Tuesday, February 27, 2007

Halotestin (fluxymesterone)

Halotestin (fluxymesterone)

Active Life: 6-8 hours
Drug Class: Highly Anabolic/Androgenic Steroid (Oral)
Average Dose: Men 20-40 mg/day
Acne: Yes
Water Retention: No
High Blood Pressure: Rare
halotestinLiver Toxic: Yes, very high
Aromatization: Debatable
DHT Conversion: No
Decrease HPTA function: Yes, moderate

Halotestin is the Upjohn brand name for the steroid fluoxymesterone. Structurally fluoxymesterone is a derivative of testosterone, differing from our base androgen by three structural alterations (specifically l7alpha-methyl, 11 beta-hydroxy and 9-fluoro group additions). The result is a potent oral steroid that exhibits extremely strong androgenic properties. This has a lot to due with the fact that it is derived from testosterone, and as such shares important similarities to this hormone. Most importantly, like testosterone, Halotestin appears to be a good substrate for the 5-alpha reductase enzyme. This is evidenced by the fact that a large number of its metabolites are found to be 5-alpha reduced androgens, which coupled with its outward androgenic nature, suggests it is converting to a much more active steroid in androgen responsive target tissues such as the skin, scalp and prostate.

The 11 beta-hydroxyl group also inhibits aromatization, making estrogen production impossible with this steroid. Estrogenic side effects such as water retention, fat fain and gynecomastia are therefore not a concern when taking this compound. Strong androgenic side effects are to be expected though, and in many cases are unavoidable. Oily skin and acne a very common for instance, at times requiring sensitive individuals to seek some form of topical or even prescription drug treatment to keep it under control. Hair loss is an additional worry, making Halotestin a poor choice for those with an existing condition. Aggression may also become very pronounced with this drug. This effect is often desired by users looking to "harness" this in order to increase the intensity of workouts or a competition. Clearly Halotestin is a strong androgen, and definitely one female athletes should stay away from. Masculinizing side effects can be intense, and may occur very rapidly with this substance. Even women daring enough to take Dianabol should think twice about this compound, as virilization symptoms are most often permanent.

Although Halotestin appears to be more androgenic than testosterone, the anabolic effect of it is not very strong. This makes it a great strength drug, but not the best for gaining serious muscle mass. The predominant effect seen when taking Halotestin is a harder, more dense look to the muscles without a notable size increase. It is therefore very useful for athletes in weight-restricted sports like wrestling, powerlifting and boxing. The strength gained from each cycle will not be accompanied by a great weight increase, allowing most competitors to stay within a specified weight range. Halotestin also makes an excellent drug for bodybuilding contest preparation. When the competitor has an acceptably low body fat percentage, the strong androgen level (in absence of excess estrogen) can elicit an extremely hard and defined ("ripped") look to the muscles. The shift in androgen/estrogen ratio additionally seems to bring about a state in which the body may be more inclined to burn off excess fat and prevent new fat storage. The "hardening" effect of Halotestin would therefore be somewhat similar to that seen with trenbolone, although it will be without the same level of mass gain. Clearly non-aromatizing androgens such as Halotestin and trenbolone can play an important role during contest preparations.

Monday, February 26, 2007

Synthroid (Levothyroxine Sodium)

Synthroid (Levothyroxine Sodium)

Synthroid is the less powerful of the two most popular thyroid replacement drugs on the market. It is synthetic T4, and is actually the more prescribed thyroid medication in America, but the lesser used of the thyroid drugs which are popular with bodybuilders. If you have naturally low T3 levels, then you may be able to supplement with T4, and have it convert to T3 via your body´s natural metabolic pathways, which involves the deiodinase enzyme. However, There have been a number of studies that have shown that during reduced caloric intake, and/or when carbohydrate intake is reduced dramatically, levels of deiodinase decline, hindering the conversion of T4 to the physiologically active T3(1). So, if you are dieting (which would necessarily mean you have a reduced caloric intake and/or reduced carbohydrate levels), then you have less deiodinase enzyme (still with me?) and thus, that T4 you are taking in hopes of getting it to convert to T3, is not getting converted. This is not what we want, clearly, and is why most pre-contest dieters include Cytomel in their drug regimen instead of Synthroid. In fact, Synthroid may be particularly bad for dieters on Cyclic Ketogenic Diets.

When you earn your living off of your body, as many fitness models, models, and bodybuilders do, it´s just too haphazard to trust Synthroid. This is especially true if you are not monitoring your Basal Body Temperature or (preferably) shelling out the money for a thyroid function test every month.

As compared to Cytomel, Synthroid requires significantly higher doses to be effective. Most bodybuilders don´t exceed 100mcgs of Cytomel during a precontest phase of dieting, but with Synthroid the doses climb significantly higher to achieve the same results. From interviews I´ve done with bodybuilders who have used Synthroid, I´ve heard of it being used at up to 300mcgs/day. When you compare that to the mere 25-100mcgs/day of Cytomel that bodybuilders are typically using, we have another strike against Synthroid. It isn´t really economically feasible to do that much Synthroid and remain cost effective, at least when compared with Cytomel. To give you a fair estimate, you could run an effective dose of both Cytomel and Clenbuterol for the same price as an effective dose of Synthroid.

My advice? Use it if you have to, but only if that´s the case, and you can´t get Cytomel or Tricana. It works, and will eventually get you to the desired body temperature for optimal fat burning, but it just isn´t as elegant as the less suppressive Tricana, or the more effective Cytomel.

References:

The effect of a low-calorie diet alone and in combination with triiodothyronine therapy on weight loss and hypophyseal thyroid function in obesity. Koppeschaar HP, Meinders AE, Schwarz F. Int J Obes 1983;7(2):123-31

Sunday, February 25, 2007

Ephedrine (ephedrine hydrochloride)

Ephedrine (ephedrine hydrochloride)

Ephedrine is a stimulant drug, belonging to a group of medicines known as sympathomimetics. Specifically it is both an alpha and beta adrenergenic agonist (you may remember Clenbuterol is a selective beta-2 agonist). In addition, ephedrine enhances the release of norepinephrine, a strong endogenous alpha agonist. The action of this compound is notably similar to that of the body's primary adrenergic hormone epinephrine (adrenaline), which also exhibits action toward both alpha and beta receptors. When administered, ephedrine will notably increase the activity of the central nervous system, as well as have a stimulatory effect on other target cells. This will produce a number of effects beneficial to the athlete. For starters, the user's body temperature should rise slightly as more free fatty acids are produced from the breakdown of triglycerides in adipose tissue (stimulating the metabolism). This should help the user shed subcutaneous body fat stores, enhancing the look of definition in the physique. The anabolic effectiveness of steroids may also be increased with this substance (mildly), as the metabolic rate is a measure of fat, protein and carbohydrate conversion by the body. An enhanced metabolic state could clearly hasten the deposit of new muscle mass.

This stimulant effect of this drug will also increase the force of skeletal muscle contractions. For this reason ephedrine is commonly used by powerlifters before a competition, as the resultant (slight) strength and energy increase can clearly improve the weight totals on major lifts. It may also provide a notable mental edge, as the user is more energetic and better able to concentrate on the tasks ahead. Many recreational weight lifters find this effect particularly welcome, and use 25-50mg of this stimulant as a regular adjunct to their training sessions. The user often feels capable of attacking the weights with much more intensity while taking ephedrine, and leaves the gym knowing they will have had a more productive workout. It is important that this compound not be used continuously for this purpose, as its effect will diminish as the body becomes accustomed to the drug. In most instances the user will take the drug only two or three times per week, usually on those days personally "important" (like chest day). The athlete is also wise to take a break (one to two months) from ephedrine treatment after several weeks have past, so as to continue receiving the optimal effect from this drug. While the strength boosting effect of this drug is noteworthy, the primary application for ephedrine remains to be as a cutting agent. The athlete will generally take this drug a few times daily during dieting phases of training, at a dosage of 25 to 50mg per application. The widely touted stack of ephedrine (25-50mg), caffeine (200mg) and aspirin (300mg) is shown to be extremely potent for fat loss. In this combination, the ephedrine and caffeine both act as notable thermogenic stimulants. The added aspirin also helps to inhibit lipogenesis by blocking the incorporation of acetate into fatty acids. The athlete will be sure this stack is working by noticing an increase in body temperature, usually a degree or so (not an uncomfortable raise). This combination is taken two to three times daily, for a number of consecutive weeks. It is discontinued once the user's body temperature drops back to normal, a clear sign these drugs are no longer working as desired. At this point increasing the dosages would not prove very efficient. Instead a break of several weeks should be taken, so that this stack may once again work at an optimal level.

Ephedrine can produce a number of unwelcome side effects that the user should be aware of. For starters, the stimulant effect can produce shaky hands, tremors, sweating, rapid heartbeat, dizziness and feelings of inner unrest. Often these effects subside as the user becomes more accustomed to the effect of this drug, or perhaps the dosage is lowered. In general, those negatively impacted by caffeine would probably not like the stronger effects of ephedrine. The mental and physical state produced by this drug is also quite similar to that seen with Clenbuterol, so those who find little discomfort with this treatment should (presumably) be fine with this item (and vice versa). While taking this drug one may also endure a notable loss of appetite, usually a welcome effect when dieting. Ephedrine is in fact a popular ingredient in combination (prescription) appetite suppressants. The user may further notice headaches and an increase in blood pressure with regular use of ephedrine. Those suffering from thyroid dysfunctions, high blood pressure or cardiac irregularities should also not be taking this drug, as it will certainly not mix well with such conditions.

As of late there is much discussion about the future availability of ephedrine. This is due to that fact that ephedrine tablets are used as the primary base for the manufacture of methamphetamine. This is you know is an illegal drug, made and sold illicitly. The structure of these two compounds is notably similar, as only a few chemicals are needed to change ephedrine into "meth". Since ephedrine is currently an over-the-counter product, underground manufacturers can easily obtain it. A trend involving large volume retail purchases for OTC ephedrine products has been developing, and many states are taking notice of it. With the widespread increase of amphetamine addiction (and related crime) ephedrine may soon join the list of federally controlled substances. While some states have already taken action to restrict the sale of this stimulant, federal action would probably be required in order have a major impact on availability. Even if a particular state is aggressively preventing the sale of these products, a thriving mail-order market still exists to fill the demand. Thumbing through the back pages of many national magazines should make this clear, as we notice advertisements for companies which ship ephedrine tablets out by the thousand.

Saturday, February 24, 2007

Fat Burning Secrets Of The Worlds Best Bodybuilders

Fat Burning Secrets Of The Worlds Best Bodybuilders


Outlaw Bodybuilder Thumbs Nose At Weight Loss "Experts" Who Earn Fortunes On The Sweat And Dreams Of Young Men & Women, And Finally Reveals The Simple Proven Science Of Fat Loss No One Else Will Tell You About...

Lifetime-Natural Bodybuilder, Personal Trainer, Nutritionist and Success Coach From New Jersey Teaches You How to Turbo-Charge Your Metabolism, Gain Muscle, Burn Off Body Fat and Develop Unstoppable Motivation ... Guaranteed! Discover How He's Taught Thousands of People to Get Leaner Faster Than They Ever Thought Possible!

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If you would like to learn how to lose body fat permanently... even in your mushiest spots... without drugs, without supplements and without screwing up your metabolism, then this will be the most important web page you will ever read. I guarantee it and I've got the results to prove it!

Who I Am And Why You Should Listen to Me

There are thousands of diet programs and dozens of people claiming to be experts. However, very few of these so-called "Fat loss experts" practice what they preach or have the credentials and track record to back up their claims. Since you're probably wondering how this program is different, here's the whole story:

I've been bodybuilding for 23 years and competing for 17 years. I've been involved in the fitness industry as a personal trainer, health club manager, nutritionist, motivation coach and freelance writer for nearly 18 years. Bodybuilding and fitness is my life - it's all I've ever done.

Outlaw Bodybuilder Thumbs Nose At Weight Loss "Experts" Who Earn Fortunes On The Sweat And Dreams Of Young Men & Women, And Finally Reveals The Simple Proven Science Of Fat Loss No One Else Will Tell You About...

Lifetime-Natural Bodybuilder, Personal Trainer, Nutritionist and Success Coach From New Jersey Teaches You How to Turbo-Charge Your Metabolism, Gain Muscle, Burn Off Body Fat and Develop Unstoppable Motivation ... Guaranteed! Discover How He's Taught Thousands of People to Get Leaner Faster Than They Ever Thought Possible!

Even if You Have Less-than Average Genetics... Even If You've Never Succeeded at Losing Weight Before... Even If You Have Stubborn Fat Deposits That Don't Seem To Budge... Right Here on This Web Page You've Found The Fat Loss Success System You've Been Looking For!

Dear Friend,

You're about to discover what might be the most powerful fat loss system ever developed. It's the same diet program fitness models and bodybuilders use to reach single digit body fat levels and achieve rock-hard muscle definition that makes them look like walking anatomy charts.

My name is Tom Venuto and over the past 14 years, through a long and painstaking process of trial, error and experimentation, I've developed a sure-fire, 100% guaranteed system for losing body fat based on the little-known nutrition secrets of competitive natural bodybuilders and fitness models.

If you would like to learn how to lose body fat permanently... even in your mushiest spots... without drugs, without supplements and without screwing up your metabolism, then this will be the most important web page you will ever read. I guarantee it and I've got the results to prove it!

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When I started the program in September, I was 248 pounds with 24% bodyfat. With Tom's information, I have been able to lose 43 pounds - all of it fat. My Body fat is now 12%. I also no longer spend $400 a month on supplements.

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What Makes This Fat Burning Breakthrough So Exciting is That it Gives You The Power To...

Lose fat permanently. It's a fact - 95% of the people who go on conventional diets gain all the weight back and sometimes they end up fatter than when they started. Now you can learn how to be in the successful 5% group that keeps it off forever. Lose body fat without wrecking your metabolism. If you've ever started a diet, then smashed into the dreaded "plateau," it's probably because you cannibalized your own muscle and slowed down your metabolism. Not only will this system teach you the only way to prevent your metabolism from crashing, you will also learn more than a dozen ways to fire up your "metabolic engine" and accelerate your body's natural rate of calorie-burning. Lose fat without drugs. When you mention bodybuilders, some people think of steroids or fat burning drugs. It's sad but true - most pro bodybuilders take them. But the joke's on them. Drugs work, but the results are temporary and the side effects are nasty. The tiny handful of natural bodybuilders who have learned how to use training and nutrition science to alter body composition without drugs are the only people in the world who keep their fat loss and muscle gains permanently. Now you can learn these fat burning secrets from a natural bodybuilding champion who knows from real-world experience exactly how it's done. Lose fat without supplements. 97% of all supplements are a total waste of money! You are being lied to and ripped off by crooked companies that don't give a rat's ass about your health and well-being. If you want to learn the ugly truth about the $13 billion per year supplement industry, and the $40 billion per year weight loss industry, then read every word of this report because it could save you thousands of your hard-earned dollars! Who I Am And Why You Should Listen to Me

There are thousands of diet programs and dozens of people claiming to be experts. However, very few of these so-called "Fat loss experts" practice what they preach or have the credentials and track record to back up their claims. Since you're probably wondering how this program is different, here's the whole story:

I've been bodybuilding for 23 years and competing for 17 years. I've been involved in the fitness industry as a personal trainer, health club manager, nutritionist, motivation coach and freelance writer for nearly 18 years. Bodybuilding and fitness is my life - it's all I've ever done.

"Tom Venuto, in my opinion, is the leading, VERY BEST fitness expert and author of our time and much of my and our client's success are due to his teachings. He and his fat loss system are on the cutting edge of science and don't miss a nutritional tip, trick, secret, or strategy in achieving amazing results. What's more, they are offered in an easy-to-understand and easy-to-follow format.

Chad Tackett, BS, CPT President/CEO Global-Fitness.com chad @ global-fitness.com

You may have seen my photos or articles in some of the magazines or on the Internet: I've been in IRONMAN, Muscular Development, Natural Bodybuilding & Fitness, Olympian's News (in Italian), Exercise for Men and Men's Exercise. I've written over 190 articles on bodybuilding, fat loss and fitness and you can find my articles featured on dozens of websites worldwide including Bodybuilding.com, Female Muscle.com, About.com, Lee Labrada's Lean Body Coaching Club, Will Brink's Muscle Building Nutrition.com, Global Health & Fitness.com, A to Z Fitness.com, and too many others to mention.

I have a BSc. degree in exercise science, I'm a certified strength and conditioning specialist (CSCS) and a certified personal trainer (NSCA-CPT). I'm a member of the International Society for Sports Nutrition (ISSN), the American College of Sports Medicine (ACSM) and the National Strength And Conditioning Association (NSCA). I'm a competitive bodybuilder and I've won three state and three regional championships. I've even gone as far as 2nd place in the Mr. Natural USA and 2nd in the Mr. Natural North America contests.

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Thursday, February 22, 2007

Primobolan® Tablets (methenolone acetate)

Primobolan® Tablets (methenolone acetate)


Quick overview:

Active Life: 4-6 hours
Drug Class: Anabolic/Androgenic Steroid (Oral)
Average Dose: Men 50-150 mg/day......Women 50-75 mg/day
Acne: Rare
Water Retention: No
High Blood Pressure: Rare
primobolan tablets pictureLiver Toxic: Very low and only in very high dosages
Aromatization: None
DHT Conversion: No
Decrease HPTA function: Low
Comments: Moderately Anabolic/Low Androgenic


This section refers to the oral Primobolan® preparation, which contains the drug methenolone acetate. It is very similar in action to the injectable Primobolan® Depot (methenolone enanthate), but obviously here the drug is designed for oral administration. At one time Schering was in fact also manufacturing an injectable methenolone acetate (Primobolan® acetate, out of manufacture since 1993), which proved to be very useful for pre-contest cutting purposes. This steroid is now gravely missed, as it was once a favorite among European competitors. Although we still have the acetate in oral form, it is a close, but not equal substitute (injection is a much more efficient form of delivery for this steroid).

Methenolone regardless of the ester is a very mild anabolic steroid. The androgenic activity of this compound is considerably low, as are its anabolic properties. One should not expect to achieve great gains in muscle mass with this drug. Instead, Primobolan® is utilized when the athlete has a specific need for a mild anabolic agent, most notably in cutting phases of training. It is also a drug of choice when side effects are a concern. A welcome factor is that Primobolan® is not c17 alpha alkylated as most oral steroid are. Due to the absence of such an alteration, this compound is one of the few commercially produced oral steroids that is not notably stressful to the liver. While liver enzymes values have been affected by this drug in some rare instances, actual damage due to use of this substance is not a documented problem. Unfortunately the 1 alkylation and 17-beta esterification of Primobolan® do not protect the compound very well during first pass however, so much of your initial dose will not make circulation. This is obviously why we need such high daily dose with the oral version of Primobolan®.

Primobolan® will also not aromatize, so estrogen related side effects are of no concern. This is very useful when leading up to a bodybuilding contest, as subcutaneous water retention (due to estrogen) can seriously lessen the look of hardness and definition to the muscles. Non-aromatizing steroids are therefore indispensable to the competitor, helping to bring about a tight, solid build the weeks leading up to a show. And of course without excess estrogen there is little chance of the athlete developing gynecomastia. Likewise there should never be a need for anti-estrogen use with this steroid. Primobolan® is also said to have a low impact on endogenous testosterone production. Although this may well be true in small clinical doses, it will not hold true for the bodybuilder. For example, in one study more than half of the patients receiving only 30-45 mg noted a suppression of gonadotropin levels of 15% to 65% a. This is a dose far less than most bodybuilders would use, and no doubt increasing it would only lead to worse suppression. One would therefore still need a testosterone stimulating drug like HCG or Clomid®/Nolvadex® when concluding a low-dose Primobolan® cycle, unless a deliberately small dose were being used.

It is also important to note that although the androgenic component of Primobolan® is low, side effects are still possible. One may therefore notice oily skin, acne and facial/body hair growth during treatment. Men with a predisposition for hair loss may also find it exacerbates this condition, and wish to avoid this item (nandrolone injectables are a much better choice). While always possible, side effects rarely reach a point where they interfere with the progress of cycle. Primobolan® is clearly one of the milder and safer oral steroids in production. Female athletes, older or more sensitive individuals and steroid beginners will no doubt find this a comfortable steroid to experiment with.

The dosage for men is somewhere in the range of 75-150mg daily. This can obviously be tedious (and costly) if one can only obtain the 5mg tablets from Mexico and S. America. A mild anabolic such as Primobolan® is often used in conjunction with other steroids for optimal effect, so some users find a slightly lower dose effective when stacking. During a dieting or cutting phase, thought to be its primary application, a non-aromatizing androgen like Halotestin® or trenbolone can be added for example. Such combinations would enhance the physique without water retention, and help bring out a harder and more defined look of muscularity. Non-aromatizing androgen/anabolic stacks like this are in fact very popular among competing bodybuilders. This compound is also occasionally used with more potent androgens during bulking phases of training. The addition of testosterone, Dianabol or Anadrol 50® would prove effective for instance, although the gains are likely to be accompanied by some level of smoothness due to the added estrogenic component.

Among women, Primobolan® is one of the most popular steroids in use. At a dosage of 50-75mg daily, virilization symptoms are extremely uncommon. One would of course not expect a tremendous amount of muscle mass with this drug, and instead should expect a slow and steady (quality) increase. Some women choose to further add-in other anabolics such as Winstrol® or oxandrolone, in an effort to increase the muscle building effectiveness of a cycle. While both of these compounds are quite tolerable to women, one must be sure not to use too high an accumulated dosage. Troublesome androgenic side effects are always a possibility with steroid use, even with very mild substances. Taken at too high a dosage, these weak anabolics can become a formidable danger to femininity. It would therefore be the best advice not to use the normal dosage range of both, but instead start with a much lower dosage of each steroid to compensate for the other. On the black market Primobolan® orals are popular, but still much less commonly found than the injectable. This is due to the higher cost effectiveness of the injectable, which uses the same active compound but with 100% bioavailability due to the form of administration.

Wednesday, February 21, 2007

Proviron

Proviron

Mesterolone Proviron (mesterolone) is basically an orally active DHT (Dihydrotestosterone) preparation. For comparision, we can think of some other orally prepared DHT compounds like Winstrol, Anavar, etc& Those both act very similarly in mechanism to Proviron, but a more accurate way to think of this compound is as something like "Oral Masteron." As I´m sure you noticed, their anabolic/androgenic ratio is very similar.Remember, DHT is 3 to 4 times as androgenic as testosterone and is, of course, incapable of forming estrogen. Also, Proviron is provironquite unique in that a simple look at it´s 4-ring structure will show us that it is not going to be too liver toxic, since it is not c17-Alpha-Alkylated, as many orals are& this modification (lacking in Proviron) makes drugs more liver toxic. Proviron has a 1-metyhl group added, instead. Looks pretty great on paper, right? Well, as usual, things tend to look better on paper than they do in the body. Your body has a negative feedback loop which prevents your body from having too much DHT floating around(if you´ve been paying attention up to now from reading my other stuff, you already know this). An excess of DHT will eventually be changed into another (largely not anabolic) compound.
And of course, being a DHT-based compound, this stuff isn´t going to be great for female athletes to use. Virilization (development of male sexual characteristics) is going to be a concern for women daring enough to try this stuff. My advice is that there is much better, safer compounds for female athletes and bodybuilders to use.



So lets go back to the comparison with being some sort of "Oral Masteron"& basically since Proviron is 5-alpha reduced and not capable of forming estrogen, and also has a very high affinity for binding to the aromatase enzyme (the enzyme responsible for converting all that good testosterone in your body into all that nasty estrogen). That means if you choose to take proviron with testosterone (and I know you wouldn´t even be doing a cycle without including some form of testosterone) and/or any aromatizable steroid, it should actually serve to prevent estrogen build up by the aforementioned binding to the aromatase enzyme, which prevents aromatase from doing it´s dirty work and making a bunch of estrogen out of the other steroids you are taking. It should also be noted that Proviron also binds very well to SHBG (Sex Hormone Binding Globulin& a hormone responsible for reducing the amount of circulating free testosterone in your body)(1). As a matter of fact, in the last study I read, it bound to SHBG better than any other drug studied. Also, I´d like to note that Proviron bound to the Anabolic Receptor better than any oral anabolic (except for the insanely toxic MethylTrienolone), having an ability to bind to the AR better then testosterone, but not as well as Nandrolone (1). Unfortunately, as we know, DHT also has a high affinity for binding to receptors in the scalp and prostate, causing some possible nasty side effects, like male pattern baldness and prostate enlargement. It´s important to remember that DHT and DHT derived compounds are used quite successfully to treat gynocomastia, and in this area, Proviron is no different.
Let´s delve into some of the positive points of this drug before we go any farther. Androgen Receptors are found in fat cells as well as muscle cells(5), and whilethey act on the AR in muscle cells to promote growth, they also act directly on the AR in fat cells to affect fat burning.(9)(3) The stronger the androgen binds to the A.R, the higher the lipolytic (fat burning) effect on adipose (fat)tissue(6)(2). As if that´s not enough good news, some steroids (notably, testosterone) even increase the numbers of A.R. in muscle and fat (9)(7). Thus, if you are taking a simple stack of proviron and testosterone, you´ll have more of the test you shoot as free testosterone floating around building muscle (compliments of the Proviron), more androgen receptors to be bound to (compliments of your testosterone) by your Proviron, thus causing more fat loss. Testosterone and Proviron are a very nice synergistic stack, pretty nearly an "ideal" stack of an oral and injectable, because both drugs will actually act to enhance the effect of the other.



So what we have here is a steroid which can basically make other steroids more effective by preventing their conversion into estrogen, as well as increasing the amount of circulating free testosterone in your body. This of course all provides a more hardened and quality look to muscles. Proviron is very much a "synergistic" drug in this respect, and it´s inclusion in any cycle would definitely make all of the other steroids perform better, and provide better gains. This is all compounded by the fact that proviron is a very lipolytic (fat-burning) drug.
Now, as if all of this weren´t enough, let´s talk about how Proviron affects your HPTA (Hypothalamic-Pituitary-Testicular-Axis)& the thing that regulates the male hormonal system. When a reasonable dose of this stuff is given (100-150mgs/day), it had no depressing effect on low or normal serum FSH and LH levels (6). Follicle Stimulating Hormone (FSH) and Leutenizing Hormone (LH) are two hormones which send a signal to your testes to produce testosterone. Good news for people considering it for PCT is that it can even raise your LH (10)! Thus, by not suppressing those hormones and maybe even raising some, your normal testosterone levels will remain intact. This points to a novel use for this compound during Post-Cycyle-Therapy for a non-suppressive "bridge" between cycles. In fact, in yet another study, administration of Proviron (basically the same dose as in the last study) produced no changes in steroids, thyroid hormones, gonadotropins nor PRL (Prolactin Levels& you want those to remain low). (8).



Unfortunately, this stuff is not too hot on it´s own. It´s a good drug for inclusion in a cycle containing testosterone and other armoatizable steroids, and it´s a good drug for a possible "bridge" between cycles. Alone, however, as an androgenic or anabolic agent, it´s effects have been very weak in both studies (9), as well as in the experience of everyone I spoke to about it. This may be due to the addition of the 1-methyl-group to DHT, which makes this stuff orally active. Whatever the case, as a stand alone anabolic or androgenic compound, it´s not too impressive.



This drug is a rare find on the American Black Market, and many Underground Labs don´t even produce it, but if you can find it, I´d say that you shouldn´t be paying more than .50cents for each 50mg tab.



Proviron (Mesterolone) Profile


[1 alpha-methyl-17 beta-hydroxy-5 alpha-androstan-3-one] Molecular Weight: 304.4716 Molecular Formula: C20H32O2 Melting Point: N/A Manufacturer: Schering Release Date: 1960 Effective Dose: 25-200mgs/day Active Life: up to 12 hours Detection Time: 5-6weeks Androgenic: Anabolic Ratio:30-40/100-150


Monday, February 19, 2007

The Implications of Cortisol Release!

The Implications of Cortisol Release!
By: David Robson

To increase muscle size and correspondingly reduce body fat one needs to ensure that all aspects of the bodybuilding lifestyle are adhered to. Essentially, a correct bodybuilding lifestyle could be best described as a complex balancing act, and to complicate matters further what works for one person may not necessarily work for another.

Diet and training are two variables most often discussed concerning muscle building and fat loss. Although diet and training are fundamentally important variables for any bodybuilding program there are many other factors at play.

Hormone release is one factor that underpins many of the physiological reactions that cause the changes in muscle density a bodybuilder desires. For example testosterone, probably the best known hormone from a bodybuilding perspective, is released following a series of hormonal processes starting in the pituitary gland (situated below the frontal lobe of the brain).

Testosterone is important because it increases muscle protein synthesis and this is essentially what bodybuilders desire most. Other important hormones are growth hormone and insulin. Growth hormone is produced in the hypothalamus, which is situated above the pituitary gland, and is responsible for keeping the body in a youthful state by revitalizing the immune system, enhancing sexual function and most importantly for bodybuilders, stimulating muscle tissue repair. Insulin assists amino acid and glucose transport into muscle cells.

The three hormones briefly mentioned are termed anabolic because of their tissue building properties and accordingly are of paramount importance for bodybuilders.

These hormones act in three different ways: drobson


They manipulate enzyme activity (enhance chemical changes in the muscle cell)

They change the speed of transport of nutrients through the cell wall.

They enhance protein synthesis.

Cortisol



However, there is another hormone closely associated with bodybuilding. This hormone is cortisol, a steroid hormone, and is probably the most underrated of the four bodybuilding hormones overviewed in this article. Cortisol is termed catabolic as it has the opposite effect to testosterone, insulin and growth hormone in that it breaks down tissue.

In fact cortisol, which is released by the adrenal glands under conditions of high mental and physical stress and high temperature, is the body?s primary catabolic hormone. The three main functions of cortisol are:


The reduction of protein synthesis.

The facilitation of protein to glucose.


The halting of tissue growth.
It is therefore essential that cortisol release is controlled if one is to facilitate muscle growth. As well as being released under conditions of stress and high temperature cortisol is also released first thing in the morning. Morning aerobics have been thought to be effective for this very reason.

However this is misguided thinking because exercising on an empty stomach first thing in the morning has been shown to actually intensify cortisol?s effects thus resulting in further muscle loss, and consequently metabolic resistance to body fat loss.

There is not a lot a bodybuilder can do in terms of completely restricting cortisol release as, although cortisol can be problematic for bodybuilders, it is an important hormone nevertheless. The vital functions that cortisol govern are the regulation of inflammatory responses in the body and the balancing of blood sugar in times of stress.

It is excess cortisol that is the problem for bodybuilders not cortisol per se. The dangers of excess cortisol are:


Reduced growth hormone, and testosterone output.

Osteoporosis.

Reduced muscle and increased abdominal fat.

Impaired memory and learning.

Reduced glucose utilization.

Impaired immunity.

Controlling Cortisol Release


Although cortisol release cannot be prevented, it can, and should, be controlled. Controlling the release of cortisol can be achieved by employing the following methods:


Exercise (aerobically and with weights): This may seem like a paradox but correct exercise, although it increases stress, will negate the effects of cortisol in the long term. The key is to not overtrain and to do just enough to adequately stimulate the particular system being training (muscular or aerobic). Aerobic sessions should be kept at between 30 and 45 minutes and weight sessions should be no longer than 45 minutes.
The endorphin release from these two types of exercise should offset any release in cortisol. Exercise will, during and straight afterward, place the body in a catabolic state but provided the sessions are not to long and nutritional needs are met a relaxed state will ultimately be achieved, and cortisol release will be controlled. Weight training also increases growth hormone which offsets cortisone release.

Nutrition: Nutrition is important at all times of the day for bodybuilders. To control cortisol release eating first thing in the morning and directly after a workout are optimum times. This is because in these most stressful times insulin does not have the nullifying effect it normally has on cortisol and diet must facilitate an insulin release directly. Both carbohydrates and protein are important at these times.

Stress management: Given that cortisol is released in response to stressful life events, whether they be of a physical or psychological nature, it is important to try to control these events. For example, it would be wise to try to relax whenever possible and to try not to overreact to trivial things like losing ones shoes etc. Every time this happens cortisol is released and gains are compromised. Think of what we could achieve if stressful events were relatively few.

Supplement with glutamine: In addition to vitamin C, glutamine may help to reduce cortisol by supplying cortisol with blood glutamine. Cortisol will not have to destroy muscle to obtain it.

Sleep: Cortisol is at its lowest and growth hormone is at its highest during slow wave sleep (deepest stage of sleep). Ensure that this stage of sleep is attained every night.

Limiting caffeine intake: As little as 2-3 cups of coffee per day can elevate cortisol levels due to the stimulating effect of caffeine.

Increase vitamin C intake: Research has shown that patients receiving 3 grams of vitamin C per day experience lower cortisol levels (Peters, Anderson & Theron, 2001).

As one trains and diets according to the dictates of tried and tested bodybuilding strategies it is well worth noting the implications of cortisol release. Its effect on the body can be deleterious if not controlled effectively and the bodybuilder should strive to employ the methods outlined in this article if success is desired.

Sunday, February 18, 2007

Testosterone Suspension

Testosterone Suspension

Testosterone suspension is simply testosterone crystals suspended in a sterile water solution. As such, it becomes active very quickly after injection, and agressiveness often sets in immediatel as well as a possible strength elevation. Since there is no ester, it also basically drops crystals into your muscle (painful), but it also gives you more bang for the buck than other forms of injectable testosterone.

As with all forms of testosterone, this product will convert to estrogen, cause some water testosteroneretention, possible acne and hairloss. Of course, testosterone will also build mass and strength faster than any other anabolic steroid as well, and should be the base of any cycle.

Reported Characteristics

Pharmaceutical Name:Testosterone
Chemical Name:4-androstene-3-one-17b-ol
Cutting/Bulking:Cutting
Anabolic Rating: 100
Active-Life: About one day.
Drug Class: Androgenic/Anabolic Steroid (For injection)
Average Reported Dosage: Men 150-1400mg weekly Women 25-50mg weekly
Acne: Yes, high
Water Retention: Yes, high
High blood Pressure: Often in higher dosages
Liver Toxic: Low
Aromatization: Yes, high
DHT Conversion: Yes-high
Decreases HPTA function: Yes
Average Price: $10/100mgs

Friday, February 16, 2007

Clomid® (clomiphene citrate)

Clomid® (clomiphene citrate)



Quick overview:
Active Life: 5-7 daysDrug Class: Selective Estrogen Receptor Modulator (Oral)Average Dose: Men 50-100 mg/dayAcne: YesWater Retention: NoHigh Blood Pressure: RareLiver Toxic: LowAromatization: NoneDecrease HPTA function: No, used to restore itStrong gonadotropin stimulator/mild anti-estrogenclomid



Clomid® is the commonly referenced brand name for the drug clomiphene citrate. It is not an anabolic steroid, but a prescription drug generally prescribed to women as a fertility aid. This is due to the fact that clomiphene citrate shows a pronounced ability to stimulate ovulation. This is accomplished by blocking/minimizing the effects of estrogen in the body. To be more specific Clomid is chemically a synthetic estrogen with both agonist/antagonist properties, and is very similar in structure and action to Nolvadex. In certain target tissues it can block the ability of estrogen to bind with its corresponding receptor. Its clinical use is therefore to oppose the negative feedback of estrogens on the hypothalamic-pituitary-ovarian axis, which enhances the release of LH and FSH. This of course can help to induce ovulation.



For athletic purposes, Clomid does not offer a tremendous benefit to women. In men however, the elevation in both follicle stimulating hormone and (primarily) luteinizing hormone will cause natural testosterone production to increase. This effect is especially beneficial to the athlete at the conclusion of a steroid cycle when endogenous testosterone levels are depressed. If endogenous testosterone levels are not brought beck to normal, a dramatic loss in size and strength is likely to occur once the anabolics have been removed. This is due to the fact that without testosterone (or other androgens), the catabolic hormone cortisol becomes the dominant force affecting muscle protein synthesis (quickly bringing about a catabolic metabolism). Often referred to as the post-steroid crash, it can quickly eat up much of your newly acquired muscle. Clomid can play a crucial role in preventing this crash in athletic performance. As for women, the only real use for Clomid is the possible management of endogenous estrogen levels near contest time. This can increase fat loss and muscularity, particularly in female trouble areas such as this hips and thighs. Clomid however often produces troubling side effects in women (discussed below), and is likewise not in very high demand among this group of athletes.



Male users generally find that a daily intake of 50-100 mg (1-2 tablets) over a four to six week period will bring testosterone production back to an acceptable level. A very common regime of dosing is; 300 md/day 1, 100 mg/day for days 2-11, and 50 mg/day for days 12-21. This raise in testosterone should occur slowly but evenly throughout the period of intake. Since an immediate boost in testosterone is often desirable, many prefer to combine Clomid with HCG (Human Chorionic Gonadotropin) for the first week or two after the steroids have been removed. The kick-start from HCG also helps to restore the normal ability for the testes to respond to endogenous LH, which may be hindered for some time after the cycle is ended due to a prolonged state of inactivity. Once the HCG is stopped, the user continues treatment with Clomid alone. HCG should not be used for longer than two or three weeks though, as the resulting increased testosterone and estrogen levels may again initiate negative feedback inhibition at the hypothalamus. When planning your ancillary drug program, it is also important to remember that injectable steroids can stay active for a long duration. Using ancillary drugs the first week after a long acting injectable like Sustanon has been stopped may prove to be wholly ineffective. Instead, the athlete should wait for two to three weeks, to a point where androgen levels will be diminishing. Here the body will be primed and ready to restore testosterone production.



Clomid and HCG are also occasionally used periodically during a steroid cycle, in an effort to prevent natural testosterone levels from diminishing. In many instances this practice can prove difficult however, especially when using strong androgens for longer periods of time. There is also no exact method for using the two drugs in this manner. Some have experimented by periodically administering small doses of HCG along with one or two tablets of Clomid, perhaps for a few days at a stretch followed by a longer break. An on/off schedule would be implemented; for fear that this combination may lose some effectiveness if used continuously for this purpose. This method of intake may prove to be effective, although it is really much more feasible to stimulate testosterone production after the cycle than to try and maintain it for the long duration during.



In addition to helping with the post-cycle testosterone crash, this drug can also help with elevated estrogen levels during a steroid cycle. A high estrogen bevel puts an athlete in serious risk of developing gynecomastia, which is an obvious unwanted side effect. With the intake of Clomid, the athlete can hopefully reduce his risk for developing gynecomastia. The estrogen "blocking" properties of Clomid appear to be slightly weaker than Nolvadex in comparison however, which is why it is not usually thought of as an equal substitute for estrogen maintenance. Of course both drugs have similar actions in the body. and are relatively interchangeable for this purpose. Clomid can likewise also be used as a maintenance anti-estrogen throughout the duration of steroid cycle with good confidence, just as is done with Nolvadex. In most instances this will prove equally sufficient, the drug effectively minimizing the activity of estrogen in the body and warding off gyno and excess water/fat retention. Unfortunately just as with Nolvadex this is not always the case however, and many find it necessary to addition another anti-estrogenic drug. The most common adjunct is Proviron, an oral DHT used to competitively lower aromatase activity and raise the androgen to estrogen ratio. The Clomid/Nolvadex and Proviron combination is extremely effective, although we could alternately replace them both with a more specific aromatase inhibitor such as Arimidex,Femara, or Aromasin. While stronger at combating estrogen in most cases, these drugs are also typically much more costly.



As for toxicity and side effects, Clomid is considered a very safe drug. Bodybuilders seldom report any problems, but listed possible side effects do include hot flashes, nausea, dizziness, headaches and temporarily blurred vision. Such side effects usually only appear in females however, as they feel the effects of estrogen manipulation much more readily than men. While female athletes can clearly gain some benefit from this substance, estrogen manipulation is probably not the most comfortable way to go about cutting up. Should it still be used for such purposed and side effects do become pronounced, the drug of course is to be discontinued and (at least) a break taken from it.
Clomiphene citrate is widely available on the black market in a variety of brand names as well as generic tabs and liquid versions.


Thursday, February 15, 2007

Primobolan

Primobolan

Primobolan is one of those anabolic steroids which has a cult following not unlike the old original version of Masteron. Actually, as you can easily see from it´s anabolic:androgenic ratio below in the profile, it´s a pretty weak steroid but actually stronger(!) than Masteron in both regards. I don´t know anyone who has run both compounds at the same dose. We are probably justified in speculating that you´d probably get similar results from either of them, when you consider the fact that you are getting quite a bit less actual drug and more ester when you choose injectable Primobolan (which has the very long Enanthate ester attached to it) over Masteron (which has the very short propionate ester attached to it). In truth, I think part of the reason many Primobolan users have been disappointed is that they failed to use enough of it, for long enough. From it´s chemical structure and anabolic:androgenic rating, we can assume it is at least as effective as Masteron, on an equal Mg for mg basis. However, due to its ester (in the injectable version), it needs to be run for at least 12 weeks to see the full benefits from it. When you consider a measly dose of 400mgs of primobolanthis stuff for 12 weeks will probably cost you around $500.


It´s easy to see why many people have tried to use less...and have been disappointed with their results. On the other hand, many competitive bodybuilders consider Primobolan indespensible to their pre-contest drud routine, and wouldn´t consider dieting without it. Anyway...I think the comparison to Masteron (another great precontest drug) is the best one we can make, with reference to expected gains and results.



I happen to be one of the few people who have used Drostanolone Enanthate (Masteron with the Enanthate ester attached) as well as Methenolone Enanthate (injectable Primobolan). I can tell you that the results from these two compounds, when ester and mg potency are the same, are in fact very similar.



Effects of Primobolan
Let´s flesh out some of the various general effects of Primobolan, before we get into the differences between the oral and injectable versions... One study performed on sheep involved administering 100mgs of Methenolone, and electronically stimulating their lats (electronic stimulation was used because they kept falling off the chin-up bars). Anyway, when compared with the lat muscles of sheep who didn´t receive Methenolone, the receiving group gained significantly more muscle mass as well as strength (1)(2). It´s also has a relatively high affinity for binding to the AR, actually binding better than testosterone (3). This ability to strongly bind to the AR may be why Primobolan is such a good "fat burner." Strong AR binding has been positively correlated with lypolysis (fat-burning) (8).



In addition, as this steroid can actually aid in reducing breast tumors, no ancillary products need be considered for use with Primobolan, and in fact, it may actually be a useful ancillary agent in it´s own right, similar to Masteron. Also, just like Masteron, Primobolan has no propensity to aromatize (convert to estrogen). Since it doesn´t aromatize, alot of the side effects commonly associated with estrogen will not be of concern. This means water retention, acne, and gyno will be non-existent more or less. this lack of water retention combined with the slow and steady gains provided by Primo may help to explain why it has earned a reputation for creating quality muscle gains. This also helps to explain why it is so expensive. Although estrogenic sides are not a concern, hair loss still, remains a very real concern with Primobolan, as with many DHT-Derived steroids. Many primobolan fans always include Finasteride and Ketoconazole (shampoo) in cycles containing Primobolan.



Although nobody would ever suggest to use Primobolan as a bulking agent, it´s been studied as an agent to halt wasting and possibly reverse many of the adverse effects of anemia. It is a shocking failure in both areas, according to some of the case studies I´ve read, (5)(6) and this should come to no surprise to anyone. Anadrol reigns supreme in this area, and nobody in the athletic community would ever compare those two drugs. However, Michael Mooney and many other respected doctors who work with AIDS patients have found sufficient evidence to claim that Primobolan is an immune enhancer and as such is very useful for AIDS patients (not that the FDA cares...Primobolan is still not approved for sale in the United States). AIDS patients aren´t really in need of Bulking Drugs, so an immune enhancer like Primo which will add small, quality gains in muscle is perfect for them. And since we aren´t even going to vaguely consider the use of Primobolan as a bulking agent, clearly this leaves us with considering it primarily for use in gaining and maintaining lean tissue. It´s a great choice for this purpose, and many competitors have used it very successfully to retain muscle while on a calorie reduced diet. The reason Primo is so useful for this purpose is that one of its primary functions is to help your body retain nitrogen (7) at a greatly enhanced rate. The greater your nitrogen retention is, the more muscle you will build. In the case of using primo as a pre-contest drug, this nitrogen retention will help you retain muscle and ensure that your dieting preferentially favors fat loss over muscle loss.



Primobolan is a very unique steroid, as it is one of the few that comes in both an oral as well as an injectable version. I suppose Winstrol does also, but Primobolan actually has a different ester on the oral (acetate ) and injectable (Enanthate) versions. The oral version is one of the more interesting oral compounds I´ve looked into. For starters, it´s one of the few compounds available to athletes and bodybuilders which is both oral as well as non-17-alpha-alkylation. This alteration is (as I´m sure you remember from other stuff I´ve written) what generally makes oral steroids survive their first pass through your liver, but also makes them Hepatoxic (Liver  toxic). Well... oral Primo doesn´t have this feature, so it is very mild on your liver (actually it basically isn´t liver toxic at all), but also is largely destroyed by it, since 17 beta estrification and 1 alkylation is the method used to make this stuff orally available. You´ll need to take a lot of this stuff for it to be effective... 100mgs/day of the oral version is a safe estimate for reasonable gains& for women, you could get away with less; perhaps 25mgs/day. Even though the acetate ester has a 2-3 day active life, your liver will do some damage to oral primo, so every day dosing will still be necessary.



When men were given a 30-45mg dose of the oral version of Primo, they experienced a 15-65% decrease in gonadotropin levels (9). Remember, I said 100mgs is a good dose for gains... well, you´ll also reduce your gonadotropin levels considerably. I have personally never understood why people recommend either oral or injectable Primobolan as a possible bridging compound for this reason... maybe at a too-low-to-do-anything dose of 10mgs it could be used as a bridge. And forget about using injectable Primo to bridge&
Hey... speaking about injectable Primo...
I´ve used this stuff at 200mgs/week and wasn´t very impressed with it. Generally, I think injectable primo needs to be used at a dose of at least 350mgs/week (100mgs/Every other Day), and preferably at a dose of 400-600mgs/week. I happen to like running it with testosterone propionate, but for convenience I would imagine most people would run it with Testosterone Enanthate, to keep dosing times the same (shooting it twice per week, in most cases).



Buying Primobolan
The unfortunate truth about injectable Primo is that it´s a very expensive chemical to obtain, and that price is reflected in the cost to the average consumer. Ten dollars per 1ml/100mg ampule is not unheard of, and I´ve seen it go for more. This is, of course, absurd. As if that´s not enough, this is also the most commonly counterfeited steroids on the black market. I recommend buying Primobolan (either the oral or injectable) from a respected Underground lab instead of trying to play a game of "spot the fake steroid" in Mexico or Europe. The underground versions should cost between $5-7 for 100mgs of Methenolone and I wouldn´t really consider paying more for it, although I have seen the British Dragon version of this product priced up to $20/ml.



Primobolan Profile
(Methenolone) (Oral Version is + Acetate Ester) (Injectable Version is + Enanthate Ester) [17beta-Hydroxy-1-methyl-5alpha-androst-1-en-3-one] Molecular weight of base: 302.4558 Molecular weight of Acetate ester: 60.0524 Molecular weight of Enanthate ester: 130.1864 Formula: C20H30O2 Melting Point: Manufacturer: Schering Effective dose(oral): (Men)50-100mgs/day; (Women) 10-25mgs/day Effective dose (injectable): (Men) 350-600mgs/week; (Women) 100mgs/week Active Life: 10-14 days (injectable); 4-6hrs (oral) Detection Time: 4-5 weeks Anabolic/Androgenic Ratio (Range): 88:44-57


Wednesday, February 14, 2007

Proviron

Proviron

Mesterolone Proviron (mesterolone) is basically an orally active DHT (Dihydrotestosterone) preparation. For comparision, we can think of some other orally prepared DHT compounds like Winstrol, Anavar, etc& Those both act very similarly in mechanism to Proviron, but a more accurate way to think of this compound is as something like "Oral Masteron." As I´m sure you noticed, their anabolic/androgenic ratio is very similar.Remember, DHT is 3 to 4 times as androgenic as testosterone and is, of course, incapable of forming estrogen. Also, Proviron is provironquite unique in that a simple look at it´s 4-ring structure will show us that it is not going to be too liver toxic, since it is not c17-Alpha-Alkylated, as many orals are& this modification (lacking in Proviron) makes drugs more liver toxic. Proviron has a 1-metyhl group added, instead. Looks pretty great on paper, right? Well, as usual, things tend to look better on paper than they do in the body. Your body has a negative feedback loop which prevents your body from having too much DHT floating around(if you´ve been paying attention up to now from reading my other stuff, you already know this). An excess of DHT will eventually be changed into another (largely not anabolic) compound.
And of course, being a DHT-based compound, this stuff isn´t going to be great for female athletes to use. Virilization (development of male sexual characteristics) is going to be a concern for women daring enough to try this stuff. My advice is that there is much better, safer compounds for female athletes and bodybuilders to use.



So lets go back to the comparison with being some sort of "Oral Masteron"& basically since Proviron is 5-alpha reduced and not capable of forming estrogen, and also has a very high affinity for binding to the aromatase enzyme (the enzyme responsible for converting all that good testosterone in your body into all that nasty estrogen). That means if you choose to take proviron with testosterone (and I know you wouldn´t even be doing a cycle without including some form of testosterone) and/or any aromatizable steroid, it should actually serve to prevent estrogen build up by the aforementioned binding to the aromatase enzyme, which prevents aromatase from doing it´s dirty work and making a bunch of estrogen out of the other steroids you are taking. It should also be noted that Proviron also binds very well to SHBG (Sex Hormone Binding Globulin& a hormone responsible for reducing the amount of circulating free testosterone in your body)(1). As a matter of fact, in the last study I read, it bound to SHBG better than any other drug studied. Also, I´d like to note that Proviron bound to the Anabolic Receptor better than any oral anabolic (except for the insanely toxic MethylTrienolone), having an ability to bind to the AR better then testosterone, but not as well as Nandrolone (1). Unfortunately, as we know, DHT also has a high affinity for binding to receptors in the scalp and prostate, causing some possible nasty side effects, like male pattern baldness and prostate enlargement. It´s important to remember that DHT and DHT derived compounds are used quite successfully to treat gynocomastia, and in this area, Proviron is no different.
Let´s delve into some of the positive points of this drug before we go any farther. Androgen Receptors are found in fat cells as well as muscle cells(5), and whilethey act on the AR in muscle cells to promote growth, they also act directly on the AR in fat cells to affect fat burning.(9)(3) The stronger the androgen binds to the A.R, the higher the lipolytic (fat burning) effect on adipose (fat)tissue(6)(2). As if that´s not enough good news, some steroids (notably, testosterone) even increase the numbers of A.R. in muscle and fat (9)(7). Thus, if you are taking a simple stack of proviron and testosterone, you´ll have more of the test you shoot as free testosterone floating around building muscle (compliments of the Proviron), more androgen receptors to be bound to (compliments of your testosterone) by your Proviron, thus causing more fat loss. Testosterone and Proviron are a very nice synergistic stack, pretty nearly an "ideal" stack of an oral and injectable, because both drugs will actually act to enhance the effect of the other.



So what we have here is a steroid which can basically make other steroids more effective by preventing their conversion into estrogen, as well as increasing the amount of circulating free testosterone in your body. This of course all provides a more hardened and quality look to muscles. Proviron is very much a "synergistic" drug in this respect, and it´s inclusion in any cycle would definitely make all of the other steroids perform better, and provide better gains. This is all compounded by the fact that proviron is a very lipolytic (fat-burning) drug.
Now, as if all of this weren´t enough, let´s talk about how Proviron affects your HPTA (Hypothalamic-Pituitary-Testicular-Axis)& the thing that regulates the male hormonal system. When a reasonable dose of this stuff is given (100-150mgs/day), it had no depressing effect on low or normal serum FSH and LH levels (6). Follicle Stimulating Hormone (FSH) and Leutenizing Hormone (LH) are two hormones which send a signal to your testes to produce testosterone. Good news for people considering it for PCT is that it can even raise your LH (10)! Thus, by not suppressing those hormones and maybe even raising some, your normal testosterone levels will remain intact. This points to a novel use for this compound during Post-Cycyle-Therapy for a non-suppressive "bridge" between cycles. In fact, in yet another study, administration of Proviron (basically the same dose as in the last study) produced no changes in steroids, thyroid hormones, gonadotropins nor PRL (Prolactin Levels& you want those to remain low). (8).



Unfortunately, this stuff is not too hot on it´s own. It´s a good drug for inclusion in a cycle containing testosterone and other armoatizable steroids, and it´s a good drug for a possible "bridge" between cycles. Alone, however, as an androgenic or anabolic agent, it´s effects have been very weak in both studies (9), as well as in the experience of everyone I spoke to about it. This may be due to the addition of the 1-methyl-group to DHT, which makes this stuff orally active. Whatever the case, as a stand alone anabolic or androgenic compound, it´s not too impressive.



This drug is a rare find on the American Black Market, and many Underground Labs don´t even produce it, but if you can find it, I´d say that you shouldn´t be paying more than .50cents for each 50mg tab.



Proviron (Mesterolone) Profile


[1 alpha-methyl-17 beta-hydroxy-5 alpha-androstan-3-one] Molecular Weight: 304.4716 Molecular Formula: C20H32O2 Melting Point: N/A Manufacturer: Schering Release Date: 1960 Effective Dose: 25-200mgs/day Active Life: up to 12 hours Detection Time: 5-6weeks Androgenic: Anabolic Ratio:30-40/100-150


Tuesday, February 13, 2007

Ephedrine (ephedrine hydrochloride)


Ephedrine (ephedrine hydrochloride)

Ephedrine is a stimulant drug, belonging to a group of medicines known as sympathomimetics. Specifically it is both an alpha and beta adrenergenic agonist (you may remember Clenbuterol is a selective beta-2 agonist). In addition, ephedrine enhances the release of norepinephrine, a strong endogenous alpha agonist. The action of this compound is notably similar to that of the body's primary adrenergic hormone epinephrine (adrenaline), which also exhibits action toward both alpha and beta receptors. When administered, ephedrine will notably increase the activity of the central nervous system, as well as have a stimulatory effect on other target cells. This will produce a number of effects beneficial to the athlete. For starters, the user's body temperature should rise slightly as more free fatty acids are produced from the breakdown of triglycerides in adipose tissue (stimulating the metabolism). This should help the user shed subcutaneous body fat stores, enhancing the look of definition in the physique. The anabolic effectiveness of steroids may also be increased with this substance (mildly), as the metabolic rate is a measure of fat, protein and carbohydrate conversion by the body. An enhanced metabolic state could clearly hasten the deposit of new muscle mass.

This stimulant effect of this drug will also increase the force of skeletal muscle contractions. For this reason ephedrine is commonly used by powerlifters before a competition, as the resultant (slight) strength and energy increase can clearly improve the weight totals on major lifts. It may also provide a notable mental edge, as the user is more energetic and better able to concentrate on the tasks ahead. Many recreational weight lifters find this effect particularly welcome, and use 25-50mg of this stimulant as a regular adjunct to their training sessions. The user often feels capable of attacking the weights with much more intensity while taking ephedrine, and leaves the gym knowing they will have had a more productive workout. It is important that this compound not be used continuously for this purpose, as its effect will diminish as the body becomes accustomed to the drug. In most instances the user will take the drug only two or three times per week, usually on those days personally "important" (like chest day). The athlete is also wise to take a break (one to two months) from ephedrine treatment after several weeks have past, so as to continue receiving the optimal effect from this drug. While the strength boosting effect of this drug is noteworthy, the primary application for ephedrine remains to be as a cutting agent. The athlete will generally take this drug a few times daily during dieting phases of training, at a dosage of 25 to 50mg per application. The widely touted stack of ephedrine (25-50mg), caffeine (200mg) and aspirin (300mg) is shown to be extremely potent for fat loss. In this combination, the ephedrine and caffeine both act as notable thermogenic stimulants. The added aspirin also helps to inhibit lipogenesis by blocking the incorporation of acetate into fatty acids. The athlete will be sure this stack is working by noticing an increase in body temperature, usually a degree or so (not an uncomfortable raise). This combination is taken two to three times daily, for a number of consecutive weeks. It is discontinued once the user's body temperature drops back to normal, a clear sign these drugs are no longer working as desired. At this point increasing the dosages would not prove very efficient. Instead a break of several weeks should be taken, so that this stack may once again work at an optimal level.

Ephedrine can produce a number of unwelcome side effects that the user should be aware of. For starters, the stimulant effect can produce shaky hands, tremors, sweating, rapid heartbeat, dizziness and feelings of inner unrest. Often these effects subside as the user becomes more accustomed to the effect of this drug, or perhaps the dosage is lowered. In general, those negatively impacted by caffeine would probably not like the stronger effects of ephedrine. The mental and physical state produced by this drug is also quite similar to that seen with Clenbuterol, so those who find little discomfort with this treatment should (presumably) be fine with this item (and vice versa). While taking this drug one may also endure a notable loss of appetite, usually a welcome effect when dieting. Ephedrine is in fact a popular ingredient in combination (prescription) appetite suppressants. The user may further notice headaches and an increase in blood pressure with regular use of ephedrine. Those suffering from thyroid dysfunctions, high blood pressure or cardiac irregularities should also not be taking this drug, as it will certainly not mix well with such conditions.

As of late there is much discussion about the future availability of ephedrine. This is due to that fact that ephedrine tablets are used as the primary base for the manufacture of methamphetamine. This is you know is an illegal drug, made and sold illicitly. The structure of these two compounds is notably similar, as only a few chemicals are needed to change ephedrine into "meth". Since ephedrine is currently an over-the-counter product, underground manufacturers can easily obtain it. A trend involving large volume retail purchases for OTC ephedrine products has been developing, and many states are taking notice of it. With the widespread increase of amphetamine addiction (and related crime) ephedrine may soon join the list of federally controlled substances. While some states have already taken action to restrict the sale of this stimulant, federal action would probably be required in order have a major impact on availability. Even if a particular state is aggressively preventing the sale of these products, a thriving mail-order market still exists to fill the demand. Thumbing through the back pages of many national magazines should make this clear, as we notice advertisements for companies which ship ephedrine tablets out by the thousand.

Monday, February 12, 2007

Anavar ® (oxandrolone)

Anavar (oxandrolone)




Quick overview:
Active Life: 8-12 hoursDrug Class: Anabolic/Androgenic Steroid (Oral)Average Dose: Men 20-50 mg/day......Women 5-15 mg/dayAcne: Only in higher dosesWater Retention: RareHigh Blood Pressure: RareLiver Toxic: Yes, c17-alfa-alkylated steroid. Due to low doses, toxicity is low to mediumAromatization: NoneDHT Conversion: LowDecrease HPTA function: Dose depandant



Anavar was the old U.S. brand name for the oral steroid oxandrolone, first produced in 1964 by the drug manufacturer Searle. It was designed as an extremely mild anabolic, one that could even be safely used as a growth stimulant in children. One immediately thinks of the standard worry, "steroids will stunt growth". But it is actually the excess estrogen produced by most steroids that is the culprit, just as it is the reason why women stop growing sooner and have a shorter average stature than men. Oxandrolone will not aromatize, and therefore the anabolic effect of the compound can actually promote linear growth. Women usually tolerate this drug well at low doses, and at one time it was prescribed for the treatment of osteoporosis. As the opinions surrounding steroids began to change in the 1980's, anavarprescriptions for oxandrolone began to drop. Lagging sales probably led Searle to discontinue manufacture in 1989, and it had vanished from U.S. pharmacies until recently. Oxandrolone tablets are again available inside the U.S. by BTG, bearing the new brand name Oxandrin. BTG purchased rights to the drug from Searle and it is now manufactured for the new purpose of treating HIV/AIDS related wasting syndrome.

Anavar is a mild anabolic with low androgenic activity. Its reduced androgenic activity is due to the fact that it is a derivative of dihydrotestosterone (DHT). Although one might think that this would make it a more androgenic steroid, it in fact creates a steroid that is less androgenic because it is already "5-alpha reduced". In other words, it lacks the capacity to interact with the 5-alpha reductase enzyme and convert to a more potent "dihydro° form. It is a simple matter of where a steroid is capable of being potentiated in the body, and with oxandrolone we do not have the same potential as testosterone, which is several times more active in androgen responsive tissues compared to muscle tissue due to its conversion to DHT. It essence oxandrolone has a balanced level of potency in both muscle and androgenic target tissues such as the scalp, skin and prostate. This is a similar situation as is noted with Primobolan and Winstrol, which are also derived from dihydrotestosterone yet not known to be very androgenic substances.

This steroid works well for the promotion of strength and duality muscle mass gains, although it's mild nature makes it less than ideal for bulking purposes. Among bodybuilders it is most commonly used during cutting phases of training when water retention is a concern. The standard dosage for men is in the range of 20-50mg per day, a level that should produce noticeable results. It can be further combined with anabolics like Primobolan and Winstrol to elicit a harder, more defined look without added water retention. Such combinations are very popular and can dramatically enhance the show physique. One can also add strong non-aromatizing androgens like Halotestin, Proviron or trenbolone. In this case the androgen really helps to harden up the muscles, while at the same time making conditions more favorable for fat reduction. Some athletes do choose to incorporate oxandrolone into bulking stacks, but usually with standard bulking drugs like testosterone or Dianabol. The usual goal in this instance is an additional gain of strength, as well as more quality look to the androgen bulk. Women who fear the masculinizing effects of many steroids would be quite comfortable using this drug, as this is very rarely seen with low doses. Here a daily dosage of 5mg should illicit considerable growth without the noticeable androgenic side effects of other drugs. Eager females may wish to addition mild anabolics like Winstrol, Primobolan or Durabolin. When combined with such anabolics, the user should notice faster, more pronounced muscle-building effects, but may also increase the likelihood of androgenic buildup.



Studies using low dosages of this compound note minimal interferences with natural testosterone production. Likewise when it is used alone in small amounts there is typically no need for ancillary drugs like Clomid/Nolvadex or HCG. This has a lot to do with the fact that it does not convert to estrogen, which we know has an extremely profound effect on endogenous hormone production. Without estrogen to trigger negative feedback, we seem to note a higher threshold before inhibition is noted. But at higher dosages of course, a suppression of natural testosterone levels will still occur with this drug as with any anabolic/androgenic steroid and therefore require post cycle therapy to restore the HPTA.



Anavar is also a 17alpha alkylated oral steroid, carrying an alteration that will put stress on the liver. It is important to point out however that dispite this alteration oxandrolone is generally very well tolerated. While liver enzyme tests will occasionally show elevated values, actual damage due to this steroid is not usually a problem. Bio-Technology General states that oxandrolone is not as extensively metabolized by the liver as other l7aa orals are; evidenced by the fact that nearly a third of the compound is still intact when excreted in the urine. This may have to do with the understood milder nature of this agent (compared to other l7aa orals) in terms of hepatotoxicity. One study comparing the effects of oxandrolone to other agents including as methyltestosterone, norethandrolone, fluoxymesterone and methAndriol clearly supports this notion. Here it was demonstrated that oxandrolone causes the lowest sulfobromophthalein (BSP; a marker of liver stress) retention among all the alkylated orals tested. 20mg of oxandrolone in fact produced 72% less BSP retention than an equal dosage of fluoxyrnesterone, which is a considerable difference being that they possess the same liver-toxic alteration. With such findings, combined with the fact that athletes rarely report trouble with this drug, most feel comfortable believing it to be much safer to use during longer cycles than most of other orals with this distinction. Although this may very well be true, the chance of liver damage still cannot be excluded, especially with hogher dosages.



At one time oxandrolone was also looked at as a possible drug for those suffering from disorders of high cholesterol or triglycerides. Early studies showed it to be capable of lowering total cholesterol and triglyceride values in certain types of hyperlipidemic patients, which initially this was thought to signify potential for this drug as a hypo-lipid (lipid lowering) agent. With further investigation we find however that while use of this drug can be linked to a lowering of total cholesterol values, it is such that a redistribution in the ratio of good (HDL) to bad (LDL) cholesterol occurs, usually moving values in an unfavorable direction. This would of course negate any positive effect that the drug might have on triglycerides or total cholesterol, and in fact make it a danger in terms of cardiac risk when taken for prolonged periods of time. Today we understand that as a group anabolic/androgenic steroids produce very unfavorable changes in lipid profiles, and are really not useful in disorders of lipid metabolism. As an oral c17 alpha alkylated steroid, oxandrolone is probably even more risky to use than an injectable esterified injectable such as a testosterone or nandrolone in this regard.

Friday, February 9, 2007

Aromasin

Anabolic Steroids Profile Aromasin Exemestane Aromasin (Exemestane) is a steroidal suicide aromatase inhibitor, which means that it lowers estrogen production in the body by blocking the aromatase enzyme, the enzyme responsible for estrogen synthesization. (1)(2)(3) This stuff was developed to fight breast cancer in post-menopausal women, who need a particularly aggressive therapy, and for whom first line defenses such as SERMS (Tamoxifen) have not worked. This should be our first clue in inferring that this stuff is pretty strong, or at least stronger than some of the other compounds which are used to fight breast cancer. Aromasin and Side Effects Aromasin averages an 85% rate of estrogen suppression (4), so it´s clearly a very effective agent for bodybuilders and other athletes wanting to avoid estrogen related side effects such as gyno, acne, or water-retention brought on by aromatizing steroids. Specifically, Exemestane dose this by selectively inhibiting aromatase activity in a time-dependent and irreversible manner (hence the "suicidal" portion of it´s name, I guess).(7) As with most of the compounds in this class, it also causes a reasonable rise in testosterone levels (6), and as you may have guessed, this rise in testosterone means that Exemestane can also cause androgenic sides(8)(9)(10). As you can see from the chart below, exemestane is very effective at both lowering estrogen (estradiol) and raising testosterone: FIG. 1. Estrogen and androgen plasma levels after 10 d of daily exemestane (25 or 50 mg) in healthy young males (mean ± SD; n = 9-11). To convert to Systeme International units: estradiol, picomoles per liter (x3.671); estrone, picomoles per liter (x3.699); androstenedione, nanomoles per liter (*0.003492); and testosterone, nanomoles per liter (x0.03467). (13) So we can see that 25mgs is a very effective dose from that chart, right? As an added benefit, exemestane not only increases testosterone and lowers estrogen, but it also increases IGF levels (11).Additionally Worth noting is that Aromasin may possibly be less harsh on blood lipids (14)than some of the other (similar) compounds we use in the world of bodybuilding or athletics (other AI´s). It also has, at best no effect on IGF, and at worst could lower (13) it. AI´s are very tricky with regards to inconsistencies in IGF levels. Unfortunately, you need to take Exemestane for a week to reach steady blood plasma levels of it, and exemestane has a ½ life of 27 hours (12.). The ability of exemestane to lower estrogen levels by the aforementioned 85% makes it a very nice choice for use in any cycle where aromatizing steroids are used. In addition, since it´s not too harsh at all on blood lipid profiles, it´s a very good choice for longer cycles. It´s ability to raise both testosterone levels also seem to suggest that it would be a very nice addition to a Post-Cycle-Therapy (PCT).

Thursday, February 8, 2007

Equipoise (Boldenone Undeclynate)

Equipoise

Equipoise (Boldenone Undeclynate), or "EQ" is one of the most widely used compounds by athletes today. Even though it is a vetrinary steroid, the quality of production is quite high due to its use in rather expensive animals. It is one of the safest and most effective steroids used today, by athletes, power lifters and bodybuilders. It can effect slow and continuous muscle mass and strength gains over a prolonged period, and generally cycles with this drug tend to be quite long because of this fact. Gains on a cutting cycle including Eq tend to be high quality lean mass, while bulking cycle gains with Eq aren't as "clean" but still have a very nice quality about them. This could be due to Eq's resistence to being converted to Estrogen, as well as DHT (technically, it converts to Dihydroboldenone).
equipoise

Equipoise (Boldenone Undeclynate) information has become much more popular in recent years since dosages hit 200mg/ml
Men get good results from a 300-600mg weekly total. In the past, this included utilizing an every other day (EOD) injection schedule, because Eq was only available in very low concentrations (50-100mgs/ml). Recently, companies like British Dragon have begun offering Boldenone in a much higher concentration (200mgs/ml) making injections much easier. Women have made excellent progress with dosages of 50-100mg total weekly doses, and this usually means a 1 injections weekly schedule. Women as a rule, seem to prefer less scar-tissue build up than men are comfortable with. In this dose range, women almost never report virilizing side effects, and usually only experienced an elevated libido. Increased hair growth on face and legs is, of course, possible (though not probable)..


Liver toxicity is not an issue with Boldenone, and it can be used for long times on either a bulking or cutting cycle, very safely. It has a reputation for appetite and red blood cell production stimulating effects, and this makes it very nice for a bulking cycle. Obviously with increased red blood cell count an increase in oxygen transport was also realized, as was improved nutrient transport, making less food become more efficient...a very nice effect for a cutting cycle.


Athletes generally stacked Boldenone with testosterone and Anadrol for mass cycles. Dianabol, due to it's close resemblance to Eq chemically, is not usually used interchangably with Anadrol in cycles containing EQ (a rare exception). Cutting, or pre-contest cycles including Boldenone often include Trenbolones, Winstrol. With the afforementioned drugs, an anti-estrogen is generally not necessary.

Reported Characteristics
Boldenone Undeclynate 1,4-androstadiene-3-one-17b-ol Cutting/Bulking:Both Anabolic Rating: 100 Active-Life: 7-9 days Drug Class: Anabolic /Androgenic steroid (for injection) Average Reported Dosage: Men 300-600mg weekly Women 50-100mg weekly Acne: Rare Water Retention: Low High Blood Pressure: Rare Aromatization: About 50% of testosterone Liver Toxic: No DHT Conversion: No (*converts to DHB) Decreases HPTA function: Yes Average Price: $150/10ml bottle

Trade Names
EQUIPOISE 200MG/ML (British Dragon) ULTRAGAN 100 100MG/ML BOLDEBAL-H 50MG/ML EQUIPOISE 25MG,50MG, /ML ULTRAGAN 50 50MG/ML GANABOL 25MG, 50MG/ML PACE 25MG/ML VENBOL 25MG/ML

Wednesday, February 7, 2007

Anabolic Workout Guide

You should take the following factors to heart since they are absolutely necessary for a successful training. What role does the use of anabolic/androgenic steroids play- Very simple: athletes who take steroids will make clearly faster, better, and greater progress than their natural colleagues. They will also obtain a much higher development stage than would have ever been possible without taking pharmaceutical compounds. Such stupid statements that one will achieve the same mass as a bodybuilder without taking steroids -it only takes longer- is nothing but a completely absurd publicity by the authorities who in their own interest conceal the truth. Read the following lines with an open-minded attitude and try to adapt this information for your own needs. 1. High-intensity training: The human organism vehemently refuses any unnecessary change since it feels best in a constant condition, a homeostasis. In order to lure it out of its passivity, several efforts and exertions must be made. The signal that the body needs in order to build up strength and muscle mass is triggered by heavy, hard, and intense training routines. These should consist of relatively few sets. Five to eight sets for large muscle groups and three to four sets for small muscle groups are completely sufficient when every set is carried out until muscle failure. 2. Training with relatively low repetitions: The body has two different types of muscle fibers: Since the muscle hypertrophy almost completely occurs in the fast-twitch white muscle fibers of type 2, a sensible bodybuilding workout must be developed in a way that these are sufficiently stimulated. For this purpose relatively few, heavy reps in the range of 6-10 are suitable. 3. Training with progressively heavier weights: In order to build up massive muscles they must be challenged and exposed to regular progressively-higher resistances. This can be achieved when the athlete continuously increases the weight during exercises. The stronger the muscles the larger their appearance. There is no mass without power. The basic exercises such as squats, bench presses, presses behind the neck, rows, barbell curls, dips, etc. are the most suitable. 4. Sufficient rest periods: The muscles are stimulated through training but only grow during their rest phase. The higher the intensity, the higher the damage of the muscle cell and the longer the resting phase. When you train with adequate intensity you simply cannot train each and every day nor should you attack a muscle twice a week. Learn to accept rest and recovery as important factors of your training success. Every day you train in the GYM should be followed by a complete off day. Bodybuilders who are interested in an optimal strength and muscle gain should train every muscle once very intensely every 7-8 days. 5. Plateau and phase training: The body can be put under maximum stress only for a limited time. If this time is exceeded, development comes to a stop and if continued the performance will regress. For this reason the intensity and extent of the training program should be changed every 12-14 weeks. The athlete should enjoy several days off training and then change to a several-week long maintenance training (plateau training). The following training program considers all essential factors which are necessary for a quick buildup of strength and muscle mass. In combination with the nutrition tips included in this book its effectiveness can be considerably increased. Based on the high intensity it is not suitable for natural bodybuilders over a long time. This training schedule is obviously only intended as a suggestion and can be changed by every athlete to meet his individual needs, as long as the discussed principles are met. Eight-Day Training Cycle: One day training, one day rest(One day on, one day off)Day 1: Chest, biceps Bench presses 3 sets 6- 8 reps Incline bench presses 2 sets 6- 8 reps Dips with added weights 2 sets 8-10 reps Barbell curls 3 sets 6-10 reps Dumbbell curls 2 sets 6-10 reps Day 3: Thighs Squats 3 sets 6-10 reps Leg presses 2 sets 8-10 reps Leg curls 2 sets 8-10 reps Day 5: Shoulder, triceps Presses behind neck 3 sets 6- 8 reps Upright row 2 sets 8-10 reps Side laterals 2 sets 8-10 reps Lying triceps presses 3 sets 6-10 reps Triceps pulley pushdown 2 sets 8-10 reps Day 7: Back. calves Chins with added weight 3 sets 8-10 reps Lat pull to neck 2 sets 8-10 reps Barbell bent-over row 2 sets 6-10 reps Seated cable row 2 sets 6-10 reps Standing calf raise 3 sets 8-12 reps Seated calf raise 2 sets 8-12 reps Note: Training is only on uneven days, i.e. every 2nd, 4th, 6th, and 8th day is a complete rest day. The intervals between the various sets should be 3-4 minutes. The athlete should pay attention that the exercises -as much as possible- are carried out with free weights and not on machines. Every muscle is directly trained only once every eight days. It is important that every set is carried out until muscle failure meaning that the athlete is unable to do another rep-etition on its own. Only in this case are the relatively few sets and especially long rest periods justified. The muscle cell must be brought in a strongly catabolic condition since only then the distinct anticatabolic effect of anabolic/androgenic steroids develops fully. The required intensity of training, however, can only be achieved when you start (after a short warmup) with the heaviest weight possible and then decrease the weight in every following set because of the losing body strength so that the desired repetitions can still be obtained. In order to avoid any misunderstandings we would like to quickly explain this principle on an example. Our athlete is able to carry out a maximum of six repetitions with 300 pounds on bench presses. 1st warmup set: 10 reps with 140 pounds 2nd warmup set: 2 reps with 200 pounds 3rd warmup set: 2 reps with 240 pounds 1st working set: 6 reps with 300 pounds 2nd working set: 7 reps with 280 pounds 3rd working set: 7 reps with 260 pounds The first warmup set serves to bring blood to the muscles and joints. The second and third warmup set are an approach to the weight of the first working set. The interplay between the muscle and nerve is stimulated, meaning the athlete gets a feeling for the heavy weights without wasting strength and energy at the same time. During the following chest exercises the warmup sets are completely omitted which means that they are only necessary for the first exercise of the muscle to be trained. Do not forget, however, that during every exercise or set you should try to squeeze out an additional one or two repetitions than during the previous training in order to in-crease training weights in the following week. This continuous tire-some struggle to increase repetitions and weight is the only way to a massive body. Always remember: HEAVY WEIGHTS BUILD BIG MUSCLES. http://www.isteroids.com/

Tuesday, February 6, 2007

Shoulder Injuries

Shoulder Injuries Most everyone have at one time or another has tweeked their shoulder. Learn how this happens, and how to avoid it !!! Shoulder injuries are very common around the weight lifting scene, especially in bodybuilding. Numerous repetitions are required by each individual deltoid head in the hopes of full and total development, all of which amplifies the risk of injury. The hip and the shoulder work in a similar fashion, but are quite different in design. The head of the femur sits deep in the glenoid cavity of the pelvis, offering a wide range of motion but not as much as the shoulder. The shoulder is a “ball and socket” joint with the humerus held within the glenoid cavity of the scapula by a complex array of musculature and tendons. Most weightlifting injuries occur when training shoulders, and believe it or not, rarely do the injuries result in muscle pulls or tears. Poor technique or over use of tendons which reinforce the articular capsule will lead to a condition of “entrapment” (when the supraspinatus tendon gets rubbed/compressed between the humerus and the top of the shoulder joint) and leads to inflammation. If this condition is not treated and/or the poor form corrected, the problem spreads, affecting the infraspinatus tendon and possibly the long head of the biceps brachii. Everyone is different. Some people have full range of motion, while others can not raise their arms laterally without friction. Sorry to say there is nothing that can be done for those people as its simply genetic predisposition. They should avoid all back presses, all extensions from the neck and lateral raises that go too high. Barbell presses should never be performed from behind the neck, from the front only, as the risk far out weighs any benefit. Muscular imbalances and misalignment can also put undue stress on the shoulder. A few visits per year minimum to an experienced sports massage therapist will help keep you properly aligned. Treat your shoulders with respect, as they can be the weakest link in the weight lifting chain. If your shoulders are unhealthy, the remaining upper body parts will suffer as well. Every experienced lifter will agree, treat your shoulders well if you want a lifetime of lifting.w

Monday, February 5, 2007

Side Effects of Steroids

Side Effects of Steroids Most of the time, when steroids are mentioned, they´re brought up as the reason a particular athlete can run so fast, hit so many home runs, or make so many tackles. They are also claimed to have extraordinarily harsh side effects and for causing severely unforgiving and permanent damage. Everybody´s seen movies like "The Program" where steroids ruin a young athlete´s life, or perhaps "The Aaron Henry Story" on HBO, where a young athlete suffers lifelong problems from his steroid abuse. Most recently, I saw the movie "Spiderman" where the villain, the Green Goblin, admits to having his superhuman strength and psychotic personality from using "performance enhancers"! I´m here to assure you that those types of horror stories are few and far between, and after consulting with literally hundreds of athletes and bodybuilders, I´ve almost never heard of anything even remotely resembling the popular "horror stories" we see in the media almost daily. I´ve certainly never seen anyone become the Green Goblin from using them, either.. By reading this article, coaches, athletes, parents and teachers will know the truth about anabolic steroid side effects and will be able to make their own informed decisions as to how bad they are. But I suspect that after reading what I have to say, as well as what the scientific literature says, the question of how bad steroids are will be a different question entirely; the only question remaining will be "why didn´t anyone tell me this before?" When I initially started research for this piece, I consulted not only real-life athletes who had vast experience with anabolic steroid use, but also scientific and medical journals. The picture that unfolded before me was very different than the one typically painted by the mass media, and certainly much different than the one I found on http://www.steroidabuse.org/, http://www.dea.org/, and http://www.drugabuse.gov/. In my research on the governmental sites, I found very little of use, to be perfectly honest. There were tons unfounded claims and talk of money being put into "studies." In reality, the government "studies" on anabolic steroids were not medical studies at all. They were surveys given to various age groups, on steroid use, in order to generate statistics. There was nothing of medical value or scientific merit on those sites, despite the endless parade of doctors that seemed to be against their use. Here´s an example of one of the more absurd claims made on one of those sites: "..[steroids] they are dangerous drugs, and when used inappropriately, they can cause a host of severe, long-lasting, and often irreversible negative health consequences. These drugs can stunt the height of growing adolescents, masculinize women, and alter sex characteristics of men. Anabolic steroids can lead to premature heart attacks, strokes, liver tumors, kidney failure and serious psychiatric problems. In addition, because steroids are often injected, users risk contracting or transmitting HIV or hepatitis.." This is the information found on a government website, in a piece written by a doctor. I´m surprised she didn´t mention turning into the Green Goblin in her list of possible health side effects. As you read what I have to say, I want you to keep this in the back of your head. I want you to remember this claim, made by a medical doctor, as you read the rest of this piece. All of the information here is exactly what has been reported to me by athletes, as well as what is found in credible scientific journals; then decide for yourself what the truth about steroid side effects is. -------------------------------------------------------------------------------- Anabolic Steroid Side Effects:1. Inhibition of Natural HormonesThe inhibition of natural hormones is probably the most common and probable side effect experienced from the use of anabolic steroids. In almost all cases, adding a hormone into your body will send a message to your endocrine system to stop producing it. This is because your body wants to remain in a very balanced state -- called "homeostasis," if I remember my high school biology class correctly. To maintain homeostasis, the body wants to avoid having too much of any particular hormone. To achieve this, the body sends a message to the testicles to slow down, or even stop producing testosterone when there is too much circulating. Unfortunately, this happens when any kind of hormone is added into the body, so even if an athlete is not using testosterone, but is using other anabolic steroids, the body will still send this signal 99% of the time. Of course different steroids cause varying degrees of inhibition ranging from total shut down of endogenous (natural) testosterone production, to very mild inhibition, where some natural hormones are still being produced and circulating. In almost all cases, this inhibition is over once the steroids aren´t active in the body anymore. In the following charts, we can see a mirror image of the level of steroid in the body (Nandrolone), compared with the level of natural testosterone being produced. In other words, as the level of steroid rises (chart 2), the level of testosterone falls (chart 1), and vice versa: Now, as that first chart shows, testosterone levels fell when Nandrolone (an anabolic steroid was administered, but interestingly, the following chart shows an almost identical mirror image, where the Nandrolone levels in the blood rise. What this indicates is that the amount of this particular steroid in the blood is directly and proportionately inhibiting natural testosterone production. Here´s the chart: Most athletes who use anabolic steroids accept all of this as a necessary price to pay in order to experience the benefits from using steroids. In an effort to combat this, athletes have experimented throughout the years with various compounds to avoid or at least limit this problem. Human Chorionic Gonadotropin, anti-estrogens, and Selective Estrogen Receptor Antagonists are all used during a cycle, or after (or both) with this goal in mind. The following is a table showing the various hormonal levels of former steroid users who haven´t used them for a year (*called "ex-abusers" by the nice people who funded the test) versus current users (*abusers): What we see in this chart is not surprising to anyone who is actually familiar with steroids, and not with media-hype. In people studied who haven t used steroids for a year, ALL of their measured hormones (testosterone, estrogen) were within the NORMAL RANGE! Clearly, the effects that steroids have on your hormones are reversible and the horror stories we ve all read in the media about people who never regained normal hormonal function after one cycle  are greatly exaggerated. I think anyone who is familiar with "After School Specials" about steroids will be very surprised at learning this fact. As for "The Aaron Henry Story" on HBO, I can t imagine how he has suffered side effects well into his 40âs when the steroid users in this study were totally fine after one year, and in some cases used more than he did! (*Journal of Steroid Biochemistry and Molecular Biology. 84 (2003) 369-375) 2. Steroid Effects and Liver DamageLiver damage is probably the most sensationalized of all side effects possible from steroid use. The media often focuses on this particular problem as if it occurs with every steroid, and in every person who takes them. Nothing could be further than the truth. Most anabolic steroids which are ingested orally pass through the liver, which functions as the body´s filtration system. When something goes through the liver, it is broken down by various enzymes, and passed along into the bloodstream. Most research on orally administered anabolic steroids focus on the fact that liver enzymes are elevated following ingestion. But does this necessarily mean that the liver is being damaged, does it? Of course not. Commonly, studies that focus on steroid toxicity often use absurd doses, or incorrectly focus on liver activity instead of damage. The liver functions as the filter for the human body.. it´s going to be activated whenever something (not just a steroid) passes through it. Does that show that steroids damage the liver? Let´s see what the scientists say.. There was an eight-week study done in 1999, which looked at the effects of an 8-week cycle of Oral steroids. The steroids examined were Halotestin (Fluoxymesterone), Dianabol (methylandrostanolone), or Winstrol (Stanozolol) on rats at the dose of 2mg/kg-body weight, administered five times a week for 8 weeks. That s almost 200mgs/day of any of those steroids, for a 200lb user. That is, I´ll speculate, much more than the average person would use on a cycle. In fact, I have never, in my years of researching steroids and speaking with athletes, heard of anybody using 200mgs/day of Halotestin, Winstrol, or Dianabol. Ever. And, at the end of that study, In vivo, each rat still had liver enzyme levels that were within normal range! (*Med Sci Sports Exerc. 1999 Feb;31(2):243-50, Rat liver lysosomal and mitochondrial activities are modified by anabolic-androgenic steroids. Molano F, Saborido A, Delgado J, Moran M, Megias A.) In another study, 16 bodybuilders using steroids were compared to 12 bodybuilders who were not. Then the bodybuilders who had used steroids stopped taking them for three months, at which points, the researchers found that liver enzymes had returned to the same levels as the non users. After only 3 months! (*Int J Sports Med 1996 Aug;17(6):429-33, Body composition, cardiovascular risk factors and liver function in long-term androgenic-anabolic steroids using bodybuilders three months after drug withdrawal. Hartgens F, Kuipers H, Wijnen JA, Keizer HA.) We can see from the chart below that ex-steroid users have totally normal liver enzymes one year after they stop using& .in fact, for some liver enzymes, even the current users have normal scores! (*Journal of Steroid Biochemistry and Molecular Biology. 84 (2003) 369-375) 3. Steroid Effects on Cholesterol (Blood Lipid Profile) Steroids can, in fact lower HDL cholesterol and raise LDL cholesterol. HDL (high density lipoprotein, commonly referred to as "good cholesterol") helps to protect the arteries by bringing unused cholesterol to the liver where it is broken down. LDL on the other hand has the opposite effect. Some steroids can therefore cause high cholesterol levels with low HDL and high LDL. Some steroids are, of course, very mild on blood lipids, while others are notably harsh. In both cases, however, it is likely that a return to within normal parameters would occur after steroids are not being taken. 4. Gynocomastia (Development of breast tissue in males)The development of gynecomastia or feminization of the breast tissue in males is possible with anabolic steroids. This is due to an excess of estrogen being present in the body, through a process known as "aromatization" whereby androgens like testosterone are converted to estrogen. This excess estrogen then finds its way to the receptors in breast tissue and binds to them. This results in the possibility of female-like breast tissue, which must sometimes be removed by surgery. Most athletes experience itchiness of the nipples, followed by pain. Since this develops over several days, usually, the athlete usually has more than enough time to discontinue the use of the compounds he´s taking, or to attempt to counteract the breast tissue development while remaining on the cycle. The two most common ways this is achieved by steroid users is either to use an anti-estrogen like Nolvadex or Arimidex in their cycle or to take Letrozole (*a very strong Aromatase Inhibitor and antiestrogenic compound) afterwards, to destroy the tissue that has developed. Male breast development occurs in basically the same way as female breast development, and the use of anabolic steroids can result in this happening at a later stage in life for males. At puberty a surplus of hormones all combine to stimulate the growth and development of breast tissue. The initiation and progression of breast development involves a variety of pituitary (and ovarian, in women) hormones, as well as various local mediators. As you can see from the following chart, testosterone has the ability to aromatize (convert to estrogen), and eventually become part of the cascade of hormones that eventually contribute to the development of breast tissue: (GYNECOMASTIA: ETIOLOGY, DIAGNOSIS, AND TREATMENT Chapter 14 - Ronald S. Swerdloff, MD, Jason Ng, MD, and Gladys E. Palomeno, MD, March 1, 2004) 5. Acne and Anabolic SteroidsAnabolic steroids can cause the Development of acne and the extent to which it is experienced can be due to a number of varying factors, with the particular steroids and exact dosages used being the two primary factors. The skin´s sebaceous glands have a particularly high affinity to Dihydrotestosterone, which is an androgen the body naturally produces from testosterone via the enzyme 5-alpha Reductase. Increased sebaceous gland activity can oily skin which can combine with bacteria and dead skin caused by normal wear and tear, eventually causing pores to become clogged more quickly than the body can remove them. This of course, is preventable by using only particular steroids, cleansing the skin regularly, and perhaps using a topical anti-androgen. (1. Am J Clin Dermatol. 2002;3(8):571-8. 2. Clin Dermatol. 2004 Sep-Oct;22(5):419-28. 3. Pol Merkuriusz Lek. 2004 May;16(95):490-2.) 6.  Roid Rage Increased aggressiveness is often claimed to occur with anabolic steroid use. Although it´s highly rare (less than 5%), significant psychiatric symptoms have been found in some steroid users, including aggression and increased violence, mania, and even psychosis. However, it must be noted that in the studies done without a control group, it can safely be assumed that naturally aggressive people simply just be more inclined to use steroids (type-A personalities, if you will). This would probably have an effect on possibly skewing the results. Certainly, if someone takes the risk to use steroids to improve their performance in a sport or their physique, they have certain aggressive traits. Can steroids enhance them? Possibly. Can steroids be to blame for anti-social, psychotic, "roid-rage" type behavior? Probably not. The evidence just isn´t there to support that. In fact, a landmark study was performed which examined different doses of testosterone administration on men aged 20-50, who had a variety of experience with steroids from having used them previously to not at all prior to the study. A variety of psychological tests were performed at the outset of the study as well as at the end. What was found was that no participant in the study had become violent as a result of the testosterone injections they had been receiving, although some said they  felt more aggressive. This clearly indicates that there is a high level of control over possible violent or aggressive behavior that can result from steroid use. The researchers also noted that in terms of the psychological tests performed, some subjects showed little or no response to testosterone, with regards to psychological measures, while others experienced significant changes. Thus, general temperment clearly plays a large role in how one responds psychologically to steroid administration. In addition, when this study was compared with others, similar results were found: Out of 109 cases studied, only 5 people exhibited Psychological (Manic or Hypomanic) effects. (*Archives of General Psychiatry, Volume 57, February 2000.) 7. Steroids and BaldnessSteroids can possibly cause men to start balding if they have a genetic predisposition towards Male Pattern Baldness. The gene for baldness is thought to reside in the X chromosome exclusively, so a good general indication of whether someone is genetically predisposed towards being bald is to look at the men on their mothers side. Chances are that if the majority of them are bald, then the person will be carrying that gene too. The reason steroids can cause premature balding is that the scalp reacts to Dihydrotestosterone (DHT) quite strongly, and many steroids can either convert to DHT or are derived from it. Of course, several anti-baldness medications can prevent this, such as Finasteride and Dutesteride. This is, of course, merely a cosmetic effect, and poses no real health issues. It could be catastrophic to a potential career with any one of a number of 80´s rock bands, but other than that, I can´t really see any real problems associated with hair loss; especially since it can be avoided when proper steps are taken and certain steroids are avoided. 8. Cardiovascular Problems from Anabolic SteroidsAnabolic steroids have been linked with cardiovascular issues. Part of this may be due to their effects on Blood Lipids (see above). But some of it is due to the fact that many steroid users have been found to have enlarged ventricles. This is actually very common in bodybuilders as well as powerlifters and other types of athletes, and is more indicative of the effect of weight training on the heart, rather than solely steroid use. 9. Virilization (Development of male characteristics in women)This term refers masculinization, or development of male sexual characteristics that females could potentially suffer from steroid use. This side effect on women is often reversible after the cycle has ended. Some typical signs of virilization are the development of a deeper voice, hirsuitism (growth of excess body hair), enlargement of external genitalia (clitoral enlargement), and possible male pattern baldness, or acne on the face or body. This is all dependent, of course, on the compounds used as well as the dosages employed. Personally, I have witnessed the most permanent of these effects to be the deepening of the voice due to the hypertrophy (growth) of the vocal chords. This is typically the most unwelcome side effect, as it makes it very obvious when a woman is using steroids. Of course, if this begins, the best course of action is to cease taking all steroids immediately. There are several ways to reverse this effect, the most common being to undergo a medical procedure known as vocal chord scraping. And yes, it´s exactly what it sounds like. 10. Stunted Growth (height)The use of some steroids can possibly stunt the growth potential of people who have not finished growing. This is only possible with certain steroids, and not with others. In fact, certain steroids have been used in clinical settings to improve growth rates in children. It is probable that the premature closure of the epiphysial cartilage, which is most likely caused by aromatizable steroids, will lead to a possible growth inhibiting effect, and could ultimately result in a shorter adult height. This most likely an irreversible side effect, as the growth plates would have sealed and can not "re-open". Anavar (Oxandrolone) has been used to improve the height of growth stunted children, and it is probable that most DHT-derived steroids could also be used for this purpose as could certain anti-estrogens. Speaking in broad terms, growth stops at the end of the teenage years...there is almost no chance to keep growing. This is because lengthening of a bone occurs at the epiphyseal growth plates (called the "growth plates" in common parlance), the remnant of the cartilage model. It's capable of proliferating. In 99.9% of humans, the process of bone elongation ends at around the mid to late teen years. At this point, the growth plates are obliterated and disappear, after which no more elongation (typified by an increase in limb length, height, etc...) can take place. Elongation of the bone occurs here and at a second epiphysis at the end. The proliferation of the cartilage happens very quickly, actually fast enough to keep ahead of the bone generation that´s "chasing" it, called ossification, which is just the replacement of cartilage by bone. As long as the cartilage growth "stays ahead" of the bone, you grow taller, as bone replaces cartilage. When the bone finally catches the cartilage (because the cartilage slows its growth rate, not the bone), it ossifies, and "seals" the growth plate. Here´s a growth plate picture, enhanced by radioactive dye (GP= Growth Plate), so you can sort of see the bone "catching" up with the cartilage. (Human Anatomy and Physiology, 6th Edition, John W. Hole jr., Wm. C. Brown Publishers.) 10. Prostate EnlargementOnce again, this is only a possibility that steroids could cause enlargement of the prostate. The media-perpetuated claim of possible prostate cancer seems to be wholly unfounded, according to most research. In many cases, this enlargement is quickly remedied upon cessation of anabolic steroid use. The first period of prostate Prostate growth, occurs first during puberty and is as a result of the testicular secretion of androgens. During adolescence to adulthood, the prostate stays at this stage, despite the relatively high levels of androgens found in the body. Then, much later on in life, there is often a second stage of growth. Although this was originally deemed to be a result of Dihydrotestosterone s actions in the body, it is more likely due to estrogen combined with a small amount of either DHT or Testosterone. Thus, it´s not hard to imagine that taking steroids can cause this type of prostate enlargement and caused trouble for a steroid taking athlete. Typically, a product such as Finasteride or Dutesteride is taken to avoid this problem, with a high degree of success. 11. High Blood PressureThis problem is possibly the most easily remedied of all steroid side effects. It s very common for steroid using athletes attempting to gain maximum bulk to abstain from all aerobic activity. This causes the body to work much harder to circulate blood. Also, the typical water and sodium retention induced by certain steroids can contribute to this. If blood pressure is measured regularly to ensure that the value is not higher than 140/90, there should be no problems. 12. Kidney ProblemsThe kidneys can undergo more possible strain during anabolic steroid intake. Kidneys are involved in some of the filtration and excretion systems of the body, and as such, when a foreign substance is administered, they necessarily work harder. Some steroid users have noticed very dark urine when on a cycle, and this is indicative of the kidneys working overtime to accomplish their goal. One of the major offenders of this seems to be Trenbolone, which turns the user s urine a very dark color unless enough water is taken in daily. Also, even though I know you re probably getting sick of hearing this from me, the possibility of side effects is dependant on both dose as well as compounds administered. Some steroids (Nandrolone) are even used to help treat people with Kidney problems! So clearly, they aren´t as bad as they´re made out to be with regards to possible kidney issues. 13. Immune System ChangesThere is a large amount of data indicating that anabolic steroids may have some effect(s) on modulating the immune system. As with most potential side effects, this is largely dose and compound dependant. There is strong evidence that different analogues produce vastly different effects on the immune system. Testosterone and certain analogues have been shown to be possibly immunosuppressive, while Nandrolone and other steroids are possibly immunostimulating. Both, however, have been found to be beneficial when given to AIDS patients, who clearly have an already compromised immune system. This is because the increase in lean body mass that those steroids can provide is consistent with an enhanced ability to fight off infections, enhanced survival rates, and a better quality of life. (1.Int J Immunopharmacol. 1995 Nov;17(11):857-63. 2. J Steroid Biochem Mol Biol. 1990 Sep;37(1):71-6 3. AIDS. 1996 Jun;10(7):745-52. 4. Journal of Neuroimmunology 83 1998, 162-67.) 14. Sterility in Males and FemalesIt´s a common side effect of steroids to cause temporary sterility in both males as well as females. In fact, anabolic steroids are so proficient at this that they have actually been studied and approved by the World Health Organization as a male contraceptive possibility. Steroids do this by disrupting the various hormones in women which potentiate the ability to have regular menstrual cycles. In men, steroids lower Follicle Stimulating Hormone to the point where normal production of sperm is not possible. This isn´t to say that nobody on a cycle has every conceived; quite the opposite, actually. There ve been legions of "happy accidents" reported to me by athletes who were on cycles and thought they couldn´t possibly conceive. Sterility caused by steroids is temporary, of course, and generally reversible by treatment with Selective Estrogen Receptor Modulators such as Nolvadex or Clomid, and/or Human Chorionic Gonadotropin. (1. Fertil Steril. 2004 Jan;81(1):226. 2. Urology. 2000 Oct 1;56(4):669.3. J Clin Endocrinol Metab. 1985 Oct;61(4):746-52 4. Fertil Steril. 1994 May;61(5):911-4. 5. Andrologia. 1985 Sep-Oct;17(5):497-501 6. Urol Clin North Am. 1986 Aug;13(3):455-63.) -------------------------------------------------------------------------------- Steroid Effects Myth: Believing Everything You HearOk, so this last side effect isn´t really a steroid effect at all. But it s true, nonetheless. It´s my hope that you read this entire article and were surprised and possibly even a little outraged. Maybe you were outraged with how casually I seem to treat a very serious topic& but more likely than not, you were outraged at the fact that most of you´ve come to think about steroids and their horrible side effects has been greatly exaggerated. The simple fact of the matter is that anabolic steroids, like any medication, can cause a host of unwanted side effects. I´m certainly not suggesting otherwise. What I am suggesting is that a more logical and rational view be taken of them. The literature suggests that these drugs are safe when used in a clinical setting; my numerous interviews and experience with athletes suggests that this also holds true outside the clinical setting. Please don´t misinterpret my position as being pro-steroid, anti-media, or anti-government. To do so would be to miss the point of this work entirely. I have the utmost respect for the media for providing the services that they do. I also have the utmost respect for the government and those who serve this country. Anabolic Steroid Side Effects are a very real and possible concern for those who decide to use them. My position, therefore, is one that I hope is consistent with both the media as well as the government s position: I simply wish to tell the truth, and allow my reader to make the best and most informed choice possible. In that regard, I think this article has served its purpose. http://www.isteroids.com/

Sunday, February 4, 2007

clenbuterol FAQ

clenbuterol FAQ Clenbuterol FAQ: Everything you need to know about Clen I wrote this because of all the confusion that surrounds this drug. Enjoy. What is Clenbuterol? Clenbuterol is a beta-2 agonist and is used in many countries as a broncodilator for the treatment of asthma. Because of it's long half life, Clenbuterol is not FDA approved for medical use. It is a central nervous system stimulant and acts like adrenaline. It shares many of the same side effects as other CNS stimulants like ephedrine. Contrary to popular belief, Clenbuterol has a half life of 35 hours and not 48 hours. Dosing and Cycling Clenbuterol comes in 20mcg tablets, although it is also available in syrup, pump and injectable form. Doses are very dependent on how well the user responds to the side effects, but somewhere in the range of 5-8 tablets per day for men and 1-4 tablets a day for women is most common. Clenbuterol loses its thermogenic effects after 6-8 weeks when body temperature drops back to normal. It's anabolic/anti-catabolic properties fade away at around the 18 day mark. Taking the long half life into consideration, the most effective way of cycling Clen is 2 weeks on/ 2 weeks off for no more than 12 weeks. Ephedrine can be used in the off weeks. Clenbuterolvs Ephedrine vs DNP Ephedrine will raise metabolic levels by about 2-3 percent and 200mg of DNP raises metabolic levels by about 30 percent. Clenbuterol raises metabolic levels about 10 percent and it can raise body temperature several degrees. DNP is by far the most effective fat burner but many people will never use it because of the risks associated with it. It also offers no anti-catabolic benefit. Although it does have anti-catabolic effect, ephedrine short half life prevents it from being all that effective. As far as side effects, Clenbuterol's are certainly milder than DNP's, and some would even say milder than an ECA stack. There is no ECA-style crash on Clenbuterol and many users find it easier on the prostate and sex drive. This may in part be due to the fact that Clen is generally used for only 2 weeks at a time. Side effects NAUSEANERVOUSNESSDIZZINESSDROWSINESSDRY MOUTHFACIAL FLUSHINGHEADACHEHEARTBURNINCREASED BLOOD PRESSUREINCREASED SWEATINGINSOMNIALIGHTHEADEDNESSMUSCLE CRAMPSTREMORSVOMITINGCHEST PAIN The most significant side effects are muscle cramps, nervousness, headaches, and increased blood pressure. Muscle cramps can be avoided by drinking 1.5-2 gallons of water and consuming bananas and oranges or supplementing with GNC potassium tablets at 200-400mg a day taken before bed on an empty stomach. Headaches can easily be avoided with Tylenol Extra Strength taken at the first signs of a headache. You may need to take double the recommended dose. Common Uses Post-Cycle Therapy: Clen is used post cycle to aid in recovery. It allows the user to continue eating large amounts of food, without worrying about adding body fat. It also helps the user maintain more of his strength as well as his intensity in the gym. Diet: Roughly the same as on cycle. Fat loss: The most popular use for Clen, it also increases muscle hardness, vascularity, strength and size on a caloric deficit. For the most significant fat loss, Clen can be stacked with t3. Diet: A high protein(1.5g per lb of bodyweight), moderate carb(0.5g to 1g per lb of bodyweight), low fat diet(0.25g per lb of bodyweight) seems to work best with Clen. Alternative to Steroids: Clenbuterol has mild steroid-like properties and can be used by non AS using bodybuilder to increase LBM as well as strength and muscle hardness. Diet: A moderate carb, high protein, moderate fat diet work well. Stimulant/Performance Enhancement: It can be used as a stimulant, but an ECA stack may be a better choice because of it's much shorter half-life. Diet: To take full advantage of the stimulatory effects of Clen, Carbs must be included in the diet. Keto diet do not work well in this case. Precautions: Is Clen for you? The same precautions that apply to Ephedrine must be applied to Clen, although some people find ECA stacks harsher than Clen. It should not be stacked with other CNS stimulants such as Ephedrine and Yohimbine. These combinations are unnecessary and potentially dangerous. Caffeine can be used in moderation before a workout for an extra kick, although its diuretic effects may shift electrolyte balance. Drink more water if you use Caffeine. What else do I need to know? Most users that report bad side effects and discontinue use are those who use high doses right at the start of the cycle. The worst side effects occur within the first 3-4 days of use. A first time user should not exceed 40mcg the first day. Example of a first cycle: Day1: 20mcgDay2: 40mcgDay3: 60mcgDay4: 80mcgDay5: 80mcg(Note: Increase the dose only when the side effects are tolerable)Day6-Day12: 100mcgDay13: 80mcg (Tapering is not necessary, but it helps some users get back to normal gradually)Day14: 60mcgDay15: offDay16: offDay 17: ECA/ NYC stack Example of a second cycle: Day1: 60mcgDay2: 80mcgDay3: 80mcgDay4: 100mcgDay5: 100mcgDay6-Day12: 120mcgDay13: 100mcgDay14: 80mcgDay15: offDay16: offDay 17: ECA/ NYC stack Do not take Clen Past 4pm and drink plenty of water: 1.5-2 gallons a day. All brands are not equal when it comes to Clen, different brands will yield different results. That about covers everything.

Steroids Like D-Bol Helped Me Build Muscle Fast

Steroids Like D-Bol Helped Me Build Muscle Fast "I am in my early 20's and have been into bodybuilding for quite awhile. I had been natural for about 3-4 years before I decided to give steroids a shot due to natural plateaus in my lifts and size. I was weary about steroid use when I was younger due to all the bogus claims about how dangerous they are, then I found out that when used properly with care they are usually perfectly safe unless high doses of orals are taken or there is a lack of preperation for a cycle of steroids. Of course, I was always reading articles about training and bodybuilding tips in muscle magazines such as Flex, MuscleMag, and Muscle and Fitness, which were my favorite 3 magazines at the time and still are. I tried all the supplements, few if any really worked except Growth Factor-1 and the Ephedrine/caffieine/aspirin stack which is illegal now but clenbuterol cleared that little problem up for me, hehe. Anyway I found a great site on the web that lists several popular, well-known and legit steroid dealers on the net for a decent price and set out to get buff and ripped in record time. For my first cycle I combined 2mL's (500mgs) of sustanon every 10 days with 30 mgs/day of 5mg thai D-bol while combining clomid to maintain natural testosterone levels while preventing gynecomastia and water retention due to estrogen conversion. The sustanon didn't really kick in until the 3rd week but the D-bol went to work immediately and I made really impressive gains right off the bat. My benchpress went up about 12.5lbs a week (for the 1st 3 weeks) of pure muscle gain along with the gains that come with water retention. I also made equally impressive gains in other areas of my body. I put on approximately 1 inch on my arms in those first 3 weeks. At week 4 I stopped the D-bol and continued with the sustanon for a full 7 weeks or so. During the rest of the cycle my benchpress went up about 7.5lbs a week with proportionate gains on other areas of my body. So, in all, my benchpress went up about 65 solid pounds (from 215lbs. to 280lbs) and my arms grew about 1 1/2 inches (I was curling 65lb. in each arm for reps) with proportionate gains throughout my physique. For my 2nd cycle I decided to kick it up a notch so I decided to go with 750 mg of sustanon a week along with 35 mg of D-bol/day for the first 3 weeks along with clomid and nolvadex to block estrogen, gynecomastia and water retention. This time I made incredible gains... for the 1st few weeks my benchpress went up about 17.5 lbs per/week along with equal gains throughout my body, especially in my arms which grew like weeds. Once the sustanon kicked in my bench went up about 10lbs per week and the rest of my body grew equally while burning about 5lbs of fat. The entire time I was consuming about 400grams of protein/day along with varied amounts of carbs and fat. I tapered off this cycle on clenbuterol which is a strong fat burner and anti-catabolic (preserves muscle from breaking down due to cortisol build up from a cycle) and t3 a strong thyroid horomone which burns fat along with trenbolone acetate (like parabolan) and masteron/winstrol for about 7 weeks. By the end of my cycle I was completely shredded and strong as an ox. I even gained alittle more strength from the trenbolone which is rated a 10 in size and strength gains with no water retention or gyno, but is hard on the kidneys. I could easily have competed in any middle weight competition and got plenty of compliments from my friends and acquaintances along with others. I was ripped at 175lbs. 5'9 in height at 5% bodyfat. I have managed to hold on to that size due to a steady dose of 250 mg of testosterone every 7-10 days and continue to bodybuild mostly for athletic reasons but the improvement of my physique is equally pleasing. This is my experience with anabolic/androgenic steroids, I hope it was informative. Take care everyone. "

Saturday, February 3, 2007

stealth injectable labs

care of EF Human Grade pharmaceuticals, produced by major pharmaceutical companies are often the first choice for most users cycles. If you are fortunate enough to be able to have a reliable source for this kind of product, then you can always be assured of getting the highest possible quality and sterility when you make your purchases. However, in recent years, Underground Steroid Labs have been making their presence felt on the the black market. This turn of events is good because it makes products more readily available to the average consumer, but it's not without drawbacks. Last month I told you about "Stealth Labs" and their revolutionary line of Stealth Injectables. This month I'm going to tell you why Stealth Labs is not just another underground lab. First, lets take a look at how *most* underground labs operate. Underground labs are all typically operated in a very similar way. Unlike what we allow at EliteFitness.com, the owner of an underground lab is a member of several discussion forums, possibly even owning or moderating one or more. Most often, the owner of a lab will use his influence on these message boards to promote his own lab over others(which is often run under a different name than the one he posts under). Often, moderators of those message boards are given free "samples" in return for their endorsement of the underground lab in question. The lesson here is that sharing your personal information, name, email, IP address, with a site that exists only to generate leads for a drug operation is not smart. Stick to sites like Elite that are legitimate businesses and make money from supplements, articles, memberships and advertising. If a community site is a front for a drug operation and they get popped, you'll be next in line. Have you ever been to a message board where "Underground Lab X" or "Underground Lab Y" is promoted by the staff heavily? It's a good bet that the owner of that lab is a member of the staff (or at least a former member of staff) on that message board. Typically, this kind of outfit, on the small Mom & Pop boards - is run the same way every time. The owner of an underground lab finds a source of powders (usually from China), buys some sterile vials and oil and a hand crimper, some capsule fillers, and they're off and running. Then they supply some people with a few free bottles of this or that, and wham! Instant underground lab, and instant "credibility". Except for being illegal, there's nothing particularly wrong with this if it's all done openly, but more often than not, these sites mislead their members and exist through a great deal of subterfuge. Although there are some underground labs which stand head and shoulders above the rest, for the most part, all underground labs offer the same products at the same prices. However, although the end product will hopefully be sterile, their drugs certainly aren't produced in a sterile lab. And, again, for the most part, quality control and lab testing on the products is never done. This is problematic, because the consumer often isn't assured of actually getting what he paid for. However, since many underground labs are owned and operated by staff members of different message boards, they have an instant (unearned) level of credibility, bought and paid for with free drugs given to staff members and moderators. This is, of course, a less than honest way to go about business and if we find one of our moderators has been corrupted, he is quickly given the boot! But this is how most underground labs operate. I spoke with my friend Anthony Roberts about this and we remarked that we have never even seen lab tests on 99% of the underground labs that are in operation today. That's why back in June, I was interested in hearing what Anthony had to say about Stealth Labs. According to Anthony, Stealth Labs is very different from most underground labs, in this respect. They not only produce high quality injectables, but they earned their reputation by providing great customer service and quality products - which is not how most underground labs operate. Last month, in the article Ketchup Packets filled with Injectable Anabolic Steroids - The Bright Future Of Injectable Steroids, I told you about how they are innovators in the field, with their high quality line of Stealth Injectables - designed to be virtually undetectable in the mail. This month I'll share with you what Anthony explained to me about why they are different than most underground labs. For starters, their raw powders are tested for purity before they begin producing a batch of injectables. They have each batch of powder tested for purity BEFORE they begin production of their injectables. This means they actually know what they're starting with, in terms of potency. Then, they take the raw powder and begin the production process in their sterile lab, under 100% sterile conditions. Everything from the conversion of raw powder into an injectable to the sealing of the product in individual sachets is done under totally sterile conditions. Finally, after they produce the sachets, a random sachet of each separate injectable is sent out to an independent lab, for testing. Only after each batch is independently tested, is the product released for sale to the general public. Here's a link where you can view those lab tests. This is one reason why Stealth Labs and Stealth Injectables have jumped to a premier position among all underground labs currently in operation today. They are committed to producing a high quality and sterile product - without all of the smoke and mirrors we usually see when a new underground lab enters the market. So how did they do it? Anthony Roberts explained it to me best, Stealth Labs entered the underground market with a product that had never been seen before and quality control methods which have rarely been seen with an underground lab.