Showing posts with label anabolic steroids. Show all posts
Showing posts with label anabolic steroids. Show all posts

Friday, January 30, 2015

GP Mast 200 by Geneza Pharmaceuticals


GP Mast 200 is an injectable steroid made by Geneza Pharmaceuticals, its active substance is Drostanolone Enanthate and Propionate.

 GP Mast 200 by Geneza Pharmaceuticals is perhaps one of the more exotic androgenic / anabolic steroids that may be used by an athlete. Originally it was developed and used as an anti-estrogen for the treatment of breast cancer. It was largely used in combination with the SERM (Selective Estrogen Receptor Modulator) Tamoxifen (Nolvadex) for the treatment of breast cancer, and did give a significant decrease in estrogen levels in women undergoing such treatment. It is not much used these days for such purposes, for varying reasons, however for many athletes including competitive bodybuilders in particular,  GP Mast 200 by Geneza Pharmaceuticals remains a rather unsung favourite of anabolic steroids medicines.

The fact that  GP Mast 200 by Geneza Pharmaceuticals was being used as an anti-estrogen goes to suggest quite a lot about some properties  GP Mast 200 by Geneza Pharmaceuticals possesses.  GP Mast 200 by Geneza Pharmaceuticals is a derivative of DHT (dihydrotestosterone) and does not convert to estrogen through means of aromatisation. It is thought that the anti-estrogenic properties of  GP Mast 200 by Geneza Pharmaceuticals may be in part to do with either an inhibition in some way of the aromatase enzyme or an interaction with estrogen itself in a way which blocks receptor binding of the estrogen. Either way, this would put  GP Mast 200 by Geneza Pharmaceuticals as a useful tool for the anabolic steroid user who uses compounds that convert to estrogen (which most anabolic tseroid users do, considering testosterone is the main basis of most cycles).

By inhibiting the aromatase enzyme,  GP Mast 200 by Geneza Pharmaceuticals would be in effect blocking the conversion of free testosterone to estrogen by the aromatisation pathway. This would not only serve to marginally increase the amounts of active free testosterone in circulation, but it would also negate the side-effects that result from high levels of estrogen due to aromatisation. Such side effects include the development of gynecomastia and water retention/bloating. Conversely, if  GP Mast 200 by Geneza Pharmaceuticals actually blocks the binding of estrogen to the estrogen receptor (ER) in some way, although aromatisation of testosterone may occur, its effects would be limited due to the inability of the estrogen to bind to the ER. Thus through this mechanism, the effects of excess estrogen production through aromatisation would also be limited by use of this steroid.

Although  GP Mast 200 by Geneza Pharmaceuticals contains such anti-estrogenic properties, it also (being a DHT derivative) has anabolic and androgenic properties. Although in theory and on paper it may be seen to be not a very strong androgen, in fact  GP Mast 200 by Geneza Pharmaceuticals does give higher androgenic effects than one may expect. The use of  GP Mast 200 by Geneza Pharmaceuticals, as it is an anabolic steroids, will shut down natural testosterone production and so despite having anti-estrogenic effects again, one must not think that  GP Mast 200 by Geneza Pharmaceuticals could be used as an option in post cycle therapy as it will inhibit recovery.

There are two forms of Masteron that are generally available for use – Drostanolone Propionate and Drostanolone Enanthate. The propionate version is usually dosed at 50-150mg/ml and is the fast acting version of Masteron, needing to be injected every other day. The enanthate version of Masteron is dosed normally at around 200mg/ml and needs only to be injected twice per week as the ester attached to the drostanolone is longer thus giving a slower release of hormone.

Due to the effects of  GP Mast 200 by Geneza Pharmaceuticals on estrogen related side effects,  GP Mast 200 by Geneza Pharmaceuticals is a very useful tool (especially in competitive bodybuilding) when cutting. As higher levels of estrogen result in water retention,  GP Mast 200 by Geneza Pharmaceuticals inhibits water retention, and many users claim that their muscles feel very full and tight on  GP Mast 200 by Geneza Pharmaceuticals, with it giving them amazing muscle pumps in the gym. Use of  GP Mast 200 by Geneza Pharmaceuticals (in combination with other appropriate meds) at low body fat levels results in the user seeing fine detail of the muscles being accentuated, such as striations and the fine details of the muscle.  GP Mast 200 by Geneza Pharmaceuticals helps draw out the water from between the skin and the muscle giving this very cut look (at low body fat levels). Not many other anabolic steroids medicines can give such effects on muscle detail as those seen with  GP Mast 200 by Geneza Pharmaceuticals.

Despite these effects of this steroid, it is a rather weak anabolic steroid in itself. One would hardly benefit at all from use of  GP Mast 200 by Geneza Pharmaceuticals on its own, and furthermore use of  GP Mast 200 by Geneza Pharmaceuticals alone may result in loss of libido due to shutdown of the body's natural testosterone production. For these reasons, it is always recommended to stack  GP Mast 200 by Geneza Pharmaceuticals with other steroids.

It is said by many that using  GP Mast 200 by Geneza Pharmaceuticals is a waste when the user has a body fat percentage higher than 10-12%. I can understand the reasoning, and the user must understand that at higher body fat levels the detail to the muscle will not be seen in such a way as described, however I do not see it as a waste due to its anti-estrogenic properties. Such properties may allow one to not use other ancillaries on cycle that would have other undesirable side effects, and in addition  GP Mast 200 by Geneza Pharmaceuticals may work in a synergistic fashion with other AS medicines to amplify their effects (for example with testosterone as described above).  GP Mast 200 by Geneza Pharmaceuticals would however not be recommended for beginner use as it is not needed at this starting out level.

An example of an excellent cutting cycle for an advanced user would be: (6-10 weeks)
  • 150mg Testosterone Propionate every other day
  • 50mg Trenbolone Acetate every day (or 100mg every other day)
  • 150mg  GP Mast 200 by Geneza Pharmaceuticals every other day50mg Winstrol every day, last 4 weeks of cycle only
As discussed,  GP Mast 200 by Geneza Pharmaceuticals possesses anti-estrogenic properties which results in the elimination of many of the unwanted side effects that AS users may experience, such as gynecomastia, water retention and dangerous increases in blood pressure. Although  GP Mast 200 by Geneza Pharmaceuticals is a weak steroid and on paper it has low androgenic properties, it has already been mentioned that in practice the androgenic properties appear to be slightly higher than in theory, and secondly  GP Mast 200 by Geneza Pharmaceuticals is a DHT derivative.

Briefly however, the side effects that may occur with use of  GP Mast 200 by Geneza Pharmaceuticals include hair loss (if prone to male pattern baldness), aggression and acne. If a user does experience acne with other androgens such as testosterone, then it is a real possibility that they may experience it with the use of  GP Mast 200 by Geneza Pharmaceuticals. I know of people who experience only a few spots with the use of testosterone however when using  GP Mast 200 by Geneza Pharmaceuticals they experience many more spots. On the other hand, there are users who seem to experience less spots on  GP Mast 200 by Geneza Pharmaceuticals than they do on Trenbolone.

Friday, September 12, 2014

Winter Bulk Cycle with Oral Anabolic Steroid for Added Mass Gains.

Bulking is an art. An art that takes a ton of effort to be successful at. Especially when you are a seasoned juicer who has already put on some mass. If you have not gained at least 20 pounds over the weight you were at before coming over to the dark side, you just have not been juicing effectively and you will be very happy with the information that follows. If you have put on a good deal of size, you will still find useful information in the following paragraphs, but for now, we will not discuss usage of other non-anbolic steroid bulking drugs such as insulin. We will get to that soon though. Keep reading!

The catch with bulking drugs is that you have to accept not being so pretty if you are to really put on some size. Water and a little fat weight have to come with adding considerable size unless you are a genetic abnormality. The most potent drugs for bulking involve the heavy androgenic drugs which also cause large amounts of water retention. All the testosterone esters, anadrol, dianabol, and deca or equipoise when combined with any of the former make for a good bulking team.

One thing you want to take into consideration with here is the mechanism by which each drugs works. Anabolic steroids are either known to have a high affinity for the androgen receptor, and thereby cause growth through this mechanism, or they have effects on growth outside the receptor. For max benefit you want to combine drugs that work by different mechanisms. All orals will work by different mechanism purely on the fact that they are ingested and not injected. The way you get a drug into your body is called the route of administration. When an oral drug is taken it must eventually pass its way through the liver. The first time it does this a few hours after you ingest the oral is the popular term, "first pass". This is just code for the first time the liver has a chance to break down the oral drug. This site of metabolism is also where the functionality of oral anabolic steroids come into play.

The 17 alkylation of oral anabolics is what makes the drug able to pass the liver and not be fully degraded. Otherwise you would be able to drink testosterone and it would work fine. We all know this is not the case. The hydrochloric acid in the stomach would destroy the testosterone molecule way before the liver even gets a chance to metabilize it. This is why the oral test "methyltestosterone" came into existence. Although it is not a very effective drug, it is highly toxic. Methyltestosterone is a prototype oral. It has the most basic of structures added to testosterone to enable its hepatic(liver) survival. They simply added a CH3 or "methyl" group to the 17th postiion on th molecule (you've most likely seen it, it is the thatched roof part of the steroid structure). The reason why I mention this is that the toxicity of orals due to their chemical make-up is not all bad. When a 17 orally alkylated drug passes by the liver, it forces the liver to kick out a little extra IGF-I each time. IGF-I is the most potent anabolic substance in the body. It is through IGF-I modulation that the use of growth hormone exerts its muscle building effects.

The moral of the story:
USING AN ORAL DRUG WILL GREATLY IMPROVE THE RESULTS OF YOUR BULKING CYCLE.
Regular old testosterone is one of the best bulking drugs there is. As long as you are not super sensitive to estrogenic side effects, this should be your staple for mass building. Novices usually use around 500mg a week of a long acting ester. More advanced bodybuilders use upwards of 1000mg a week. The best way to do this is to find yourself some cheap multi-dose vials of a long acting test like enanthate. But I'm not "telling you to do this", ummm...this is for information purposes only...ok...hypothetically...If you use a shorter acting ester like propionate, it will be much more painful to administer and you will definitley not administer this amount. Prop at 100mg eod is more the norm for novices, 100-200mg daily for advanced. Prop usually comes 100mg/cc, two cc's in one shot of prop hurts!! You will definitely experience some welting if you try this. I do not recommend it. You will either be limping or rubbing your shoulder almost daily. This is miserable. Long acting esters like sustanon, enanthate, cypionate, etc. do not cause this extrem discomfort. Please keep this in mind.

Okay, so we have an oral, either Dianabol or Anadrol, with an injectible testosterone, and now you need a even blood level anabolic like deca or equipoise. Either one will suffice. Remember though, as we've said before, combining aromatizing drugs such as anadrol testosterone esters with progestagenic drugs such as anadrol is very risky for all but those who are not susceptible to gyno. So be careful. Even if you have used androgenic drugs such as test before with no chest soreness, be careful. If you decide to do this, you will want at least one estrogen on hand for precautionary reasons.

Assuming all is well, and you choose to take this aggressive technique, you will need at least a 2mg/lb of bodyweight per week of the injectible anabolic. You could technically use primo or winstrol as well for a little less overall bloat. The dosage patterns will be different with these drugs if used for this purpose and we will talk about this in the future. For now lets assume either Deca Durabolin or Equipose. Deca Durabolin at 300-400mg/week is often used by novices, 600-800mg for advanced. In all the athletes I have known, I have not seen a reason to go above 500mg when combining Deca Durabolin or Equipose with both an oral and a testosterone ester. This dose should be more than enough to get you gaining and keep your joints from aching while you push all that heavy iron (we will get into joint/ligament/tendon properties of anabolics soon).

Thursday, August 14, 2014

Winstrol – Injectable Vs Oral


Winstrol can be used as either an oral or an injectable steroid. It is important to find out about both methods because you will get different results depending on the way you decide to administer it. The steroid Winstrol comes from the base structure of DHT. This is simply testosterone with 5alpha reduced. The c4-5 double bond has been removed using two hydrogen atoms. DHT does not aromatize into estrogen. While both forms of Winstol are the same the oral type offers a micronized Stanozolol powder that is suspended in water.

Winstrol offers a couple of modifications – c17methylation so that it can get past the liver on the first pass. A pyrazol group is added as well giving it a 5 sided group of Cyclopentane. The anabolic rate of Winstrol is very high with 320% testosterone. This results in the individual gaining strength and losing fat as long as they maintain a strict diet.

Winstrol comes from DHT and it is known to have antestrogenic effects. It also features anti-progestenic properties that block the receptors. The hard look your physical appearance takes on from Winstrol is the result of the estrogen and progesterone. The body looks very smooth as a result. It is important for you to know that it is 17aa meaning it is toxic to the liver. It is even more toxic to the liver when the method used is injection. This is because when a drug is consumed orally it takes a first pass into the liver so that only a portion of it actually gets into the blood stream.

In most cases, the first pass of Winstrol will take place in the gut and the liver. After it has been metabolized it will enter the bloodstream. Any blood that is metabolized in the gastrointestinal tract won’t go directly to the heart. Instead it passes from the liver to the hepatic vein through the portal vein. The liver is the system in your body responsible for filtering excess nutrients, toxins, and various substances that shouldn’t be in your bloodstream.

Oral steroids including Winstrol must first make a pass through the metabolism in the intestines and then again in the liver. Some of the various oral steroids are able to be absorbed intact while others are absorbed after metabolic activity has taken place. During the first pass is completed the drug is allowed to move through the body until another tissue absorbs it.

You will find some huge differences between the body’s reaction to the injectable and the oral methods of consuming Winstrol. The injectable option allows it to be placed directly into the bloodstream so it only has to go through the second pass metabolism while the oral version has to go through the gut and the liver before it is circulated into the bloodstream.

If you choose to inject Winstrol you will get more nitrogen retention than taking the oral version. This allows more muscle tissue to grow. If that is your goal then of course you will want to use the injectable method. They oral method does offer some good advantages though. Taking this first pass though allows the drug to be exposed to various enzymes and proteins.

To help you understand they synergy between Winstrol and the other steroids out there let me offer you some information on Sex Hormone Binding Globulin (SHBG). This is a Glycoprotein that is produced in the liver. More than half of the testosterone in your body is actually SHBG, and you can lower the amount of it when you consume Winstrol. A dose as low as .2mg per kg of body weight will help you reduce the amount of SHBG by 50%.

You may be wondering why you can’t get the same results with the oral method. This is because of the first pass it has to take through the liver. The Winstrol interacts with SHBG that is produced in the liver. It doesn’t go through the bloodstream first. Studies have shown that the injectable method of Winstrol is more effective than the oral when 700 mgs are injected per week vs. 400 mgs per week consumed orally.

For women, the opposite is true – they need to use the injectable method of Winstrol. The oral version offers need more synergy in their cycles but women want to avoid this. When women have less SHBG they have more testosterone and that can lead to hirsuitism which is an abnormal growth of body hair. It can also affect their menstrual cycle. Some women find their clitoris becomes enlarged and they suffer from severe acne when they use the oral method of Winstrol.

It is common for males who use the oral method of Winstrol to have more acne as well. Both men and women need to watch for liver toxicity issues as well. This steroid has one of the highest occurrences of that. The best advice I can give you is to use Winstrol if you like, but don’t use too much of it and don’t use it too often.

Friday, July 18, 2014

Women and Trenbolone Use


Trenbolone is one of the most por drugs used by bodybuilders today and, when you look at the stats, it is not hard to see why. A very potent androgen with strong anabolic activity, Trenbolone is an extremely effective hardening and cutting agent. In fact, it is considered indispensable when it comes to pre contest preparation. However, it is also extremely valuable in the off-season as it creates a rapid build up of strength and muscle mass. In fact, the anabolic effect is often compared to testosterone or Dianabol with one very important difference - it does not convert to estrogen. This is what truly sets it apart, as most mass building drugs readily aromatize, leading to many estrogen related problems (e.g. water retention gynecomastia).

Due to the lack of water retention, the gains when using this drug are more easily maintained on discontinuing its use. In addition to this, a very hard and defined appearance can be achieved. Also, since gynecomastia is not an issue, there should not be any need to add an anti-estrogen as long as Trenbolone is the only steroid being used. Due to the highly androgenic nature of this drug an increase in the burning of body fat is observed and a much tighter physique can be achieved without having to resort to extreme dieting.

Trenbolone is more potent than testosterone with an effect being gauged as three times as strong on a milligram for milligram basis. It is also four times as anabolic as Deca-Durabolin - nandrolone decanoate - Durabolin and ten times as androgenic. This makes the majority of the weight gained on this drug lean, quality muscle. Trenbolone also creates an increase in the levels of the hormone IGF-1 (Insulin like Growth Factor-1) which is highly anabolic within muscle tissue. Trenbolone has a stronger binding affinity to the androgen receptor than testosterone. This feature is a major contributing factor to the process of anabolism and fat loss. By promoting nitrogen retention and protein synthesis within the muscle Trenbolone allows the food you eat and the nutritional supplements you take to be used more effectively. It also reduces levels of the catabolic hormone cortisol. Trenbolone is also involved in the production of red blood cells and increases the rate of glycogen replenishment (both of which contribute not only to stamina but also to recovery from workouts)

A reduction in aerobic capacity is the most common complaint with Trenbolone. This is thought to be caused by bronchial dilation resulting from an increase in prostaglandin production. The condition known as "trenbolone Cough" is often a complaint registered with users of the Acetate version (Trenbolone is available in Acetate and Enanthate forms). Androgenic side effects may also be experienced which include oily skin, aggressive behavior, and acne and hair loss. For this reason women are usually advised to stay away from this drug.

It seems that although women are generally told to avoid using this drug, Trenbolone is being used more and more by women in controlled doses. The fact that it adds primarily lean mass whilst reducing body fat is obviously a key factor in its attractiveness. When women were asked for their feedback on Trenbolone use a variety of favored dosages came up. Anything from a very conservative 10mg every other day to a more adventurous 100mg/week split into two doses.

Stacking Trenbolone with Testosterone Propionate was also something favored by those engaging in high level competition. Another use of Trenbolone involved taking it 3-4 days before a show in order to add hardness and definition to the physique. It has to be said that side effects were experienced by all - usually increased hair growth and acne - and the severity of the side effects seemed to be worse in younger women. The theory expressed here being that ovarian function may be the reason for this, with a younger woman still having stronger ovarian function than an older women who may be entering peri-menopause. This is all speculation of course but seems like a plausible explanation in my opinion. Either way, if you are considering using Trenbolone it is advised to use it on its own and at extremely low doses (such as the aforementioned 10mg every other day) in order to test your own unique sensitivity.

Trenbolone is a potent androgen that is primarily used in cattle, so there is even less information at our disposal on this compound or its effects on the female endocrine system than any other drug. It is the one drug that seems to produce results as significant as the side effects that are associated with it. Women are generally advised to stay clear of Trenbolone considering the strong androgenic component which eradicates any possibility of running Trenbolone without sides. The more seasoned female athlete will run it in the off season in order to reap the muscle building benefits of the drug whilst maintaining a relatively low body fat. On the other hand running it during contest preparation will preserve the newly added muscle mass while on a calorie restricted diet. The less daring athlete will run Trenbolone during the last few weeks of contest preparation or even limit their use to the week before the show - with a more frequent injection schedule.

Women who have experienced less favorable side effects on Trenbolone report experiencing tachycardia from a single pin, accompanied by profuse night sweats and insomnia bad enough to bail on the cycle. Others experience rapid hair growth with more frequent shaving (side effects that are far from unmanageable).

Quite honestly, Trenbolone dosing is dependent on how much a woman is willing to deal with in terms of sides. There is no conservative dose for a first timer with Trenbolone being far better suited for the educated, experienced and seasoned athlete who has paid her dues.

It is also important to note that Trenbolone lowers TSH levels so running T3 in conjunction with it is highly advisable, as well as an anti-prolactin such as Dostinex at 0.5mg every third day or 5mg of Bromocriptine daily to keep prolactin levels in check.

Friday, July 11, 2014

GP Stan 50 (Winstrol tabs) by Geneza Pharmaceuticals


GP Stan 50 by Geneza Pharmaceuticals is an oral steroid which contains 50mgs of the hormone stanozolol.

This is the same substance that is suspended in water in GP Stan 50 inj.. The oral preparation of this substance allows bodybuilders to avoid the discomfort of everyday injections which are the normally the protocol with the injectable version. Due to the fact that taking this product with food can cause absorbtion problems, it is recommended that one take GP Stan 50 on an empty stomach for best results. Some bodybuilders also choose to split up their dosage of GP Stan 50 throughout the day in an effort to keep blood levels as consistent as possible.

Winstrol , as it is most popular referred to, is one of the most popular steroids in use today. This drug has very low androgenic properties and very high anabolic properties. GP Stan 50 does not have the ability to aromatize and therefore will not cause any water bloat. This has made this steroid very popular with bodybuilders in the cutting phase of their training.

Users of winstrol often report good gains in strength, vascularity, and muscle tone. People often report very intense muscle "pumps" during workouts when using this compound. This can be attributed to the dynamic protein synthesis and nitrogen retention brought about by the use of this steroid. Some studies have also shown that winstrol has estrogen and progesterone blocking abilities, making it a good choice to use with other steroids such as Testosterone , Deca or Trenbolone.

Winstrol also does a very good job of reducing the amount of SHBG in the body, thus allowing other steroids to be much more abundant in their free state in the body. Due to this fact, GP Stan 10 makes a great addition to all cycles. Winstrol is a C17-alpha alkylated compound, and therefore can be toxic to the liver over time. Because of this, it is recommended that bodybuilders using this compound try to keep dosage in a reasonable range and limit cycle duration to 10wks. There are also several liver protectants and detoxifiers available which should be considered when doing a cycle of this steroid.

Due to its low androgenic activity, GP Stan 50 is a very good choice for women bodybuilders. Males typically use GP Stan 50 in dosages of 40-100mgs a day for a period of 6-8 weeks. 5-10mg a day for a period of 4-6 weeks is the normal dosage range for women.

Friday, July 4, 2014

Recommended Recovery Time Between Anabolic Steroid Cycles


The first factor is that recovery of the HPTA (hypothalamus, pituitary, and testicular axis) from one cycle should always occur fully before starting the next.

Where an anabolic steroid cycle is very short, such as only 2 weeks, steroid cycle recovery can be almost immediate. Well-planned, moderate length steroid cycles, such as only 8 weeks, often allow recovery in a time frame such as only 2 weeks. Long steroid cycles, such as 12 weeks or longer and especially 14 weeks or longer, or poorly planned cycles often have very protracted recoveries.

So first, regardless of what is written below with regard to timing, you should wait until natural testosterone production, without aid of any drug, is back to midnormal levels or better.

Other than this, the time between steroid cycles should be related to duration of anabolic steroid use, including time of clearance after the last injection. Another way of looking at that is the balance between the number of weeks that anabolic steroids are used versus the number of weeks that no steroid is being used.

There really are no black/white cutoff values that anyone can give. Time off versus time on is a gradually sliding scale.

Broadly speaking, I put it this way though: Being “off” twice as many weeks as being “on” is entirely conservative for most who are seeking to build muscle, and absolutely can give great results. Really the only reason to be more conservative than this is if wishing only to maintain. Being “off” about as many weeks as being “on” is moderately aggressive. When the cycles are well-planned, there’s generally no problem with this and, of course, this can give somewhat faster results than the above. And being “off” only half as many weeks as being “on” is about as aggressive as I recommend for the health conscious person. Proper recovery should of course be verified, and blood tests become more important at this frequency of use.

So there’s no one answer, but the above general description has over time proven helpful for many to decide where they wanted to be.

Friday, June 27, 2014

Anabolic Steroids, High Blood Pressure, and the Kidneys


When discussing anabolic steroid use and its known side effects, it is not uncommon to see bodybuilders express concern over potential liver injury or other cardiovascular health issues. However, we are now starting to see a much larger contingent of our community suffering from an equally serious, although less frequently recognized side effect in kidney disease/failure. This is a fairly recent phenomenon, which started in earnest about 10-15 years ago. Although there were certainly documented cases of kidney disease/failure prior to this, they were not nearly as prevalent as they are today. Although there are many potential causes of kidney failure, in this article we are going to limit ourselves to those most often attributed to the bodybuilding lifestyle.

Unfortunately, there is no single cause associated with kidney failure in bodybuilders. Often, it is an accumulative effect brought on by the presence of multiple stressors affecting the body at one time, but before we can pinpoint these causes, we must first understand how steroids affect the body, as well as possess a basic understanding of how the kidneys work to protect the body from toxins.

The kidneys are two bean-shaped organs which sit below the ribcage; one on each side of the spine. Their primary job is to filter the blood of toxins, which they do at a rate of roughly 120-150 quarts of blood per day. From this, they produce about 1-2 quarts of urine, which is then transported from the kidneys to the bladder for disposal.

The kidneys do not work as single, large filtering mechanism. Rather, each one contains about 1 million tiny filtering units called nephrons, which work to purify the blood at a microscopic level. Each of these nephrons contains a tubule, as well as its own filter (called a glomerulus). Just as the digestive system works in a multi-step process to break down food for absorption, nephrons also work through 2–step process to filter the blood. As blood moves through the glomerulus, it allows fluid and waste products to pass through it, while preventing large molecules, such as blood cells and proteins, from doing so. Afterward, this pre-filtered fluid is then sent through the tubules, which further refines the blood by separating toxins from beneficial substances, such as minerals. Ultimately, everything useful is sent back into circulation, while the final concentrated waste product becomes urine.

Let’s pause there for a second and transfer our attention over to a common side effect associated with anabolic steroids use—high blood pressure. Anabolic steroids have been thought to increase blood pressure through a variety of possible mechanisms, but it is their sodium retaining properties which are the primary cause of high blood pressure in most users. When anabolic steroids are administered they inhibit an enzyme known as 11-beta hydroxylase, which leads to the increased production of deoxycorticosterone and the subsequent retention of sodium and water. While anabolic steroids can vary substantially in their ability to influence this enzyme, as a general rule, the higher the dose employed, the more this enzyme is inhibited. Therefore, high dose users are more likely to experience elevated blood pressure compared to low-dose users.

High blood pressure is frequently implicated as a risk factor in cardiovascular disease and rightly so, but what about its effect on renal (kidney) function? Unfortunately, high blood pressure is a direct cause of renal stress and a leading contributor in the development of kidney failure. In fact, high blood pressure is the #2 cause of kidney failure in the United States right behind diabetes, being responsible for a full 28+% of documented cases and this number has only continued to grow over the last decade. With high blood pressure being one of the most common side effects associated with anabolic steroids use, one might think that it would garner more attention among the drug using community, but sadly, it does not.

When blood pressure is high, blood vessels stretch so that blood can flow more easily. This chronic stretching eventually weakens and scars the blood vessels of the kidneys, damaging them and impairing their ability to work properly. Once damaged, they become inefficient at waste and fluid removal. On top of the resulting toxin build-up, the inability to remove excess fluid can elevate blood pressure even more, resulting in a dangerous cycle.

Although anabolic steroids use alone is a potentially significant contributor to kidney disease/failure, as mentioned above, there are usually multiple causes involved in its development. Another potential risk factor is the use of nephrotoxic agents, such as NSAID’s. With anti-inflammatory drugs like Ibuprofen being routinely implicated in the development of kidney disease/failure and with many bodybuilders regularly using these drugs to treat various aches and pains, this risk factor should not be ignored. For anabolic steroids using bodybuilders, the over-use of NSAID’s may be all it takes to enter stage 1 kidney failure, followed by entrance into the later stages if not addressed. Therefore, nephrotoxic drugs should be used sparingly and only as needed. In cases of chronic pain and inflammation, one should seek speak with their physician regarding alternative treatments.

If you have been around the bodybuilding nutrition scene for any length of time, you will be familiar with the warnings associated with a high protein diet. While numerous studies have demonstrated the relative safety of a high protein diet, excess protein intake will still place additional strain on the kidneys. While this is not an issue in otherwise healthy people, it is like throwing gasoline on a burning fire in those with already compromised kidney function.

This is good reason to rely on the protein-sparing effects of carbohydrates and fats in the off-season, rather than using excess protein to meet one’s caloric demands. There has yet to be any published research demonstrating the benefits of a very high protein diet for the purpose of muscle growth, but perhaps we should first define the term “very high protein” diet. Among bodybuilders, 1-2 grams of protein per pound of bodyweight is considered to be typical in terms of daily protein intake.

In my opinion, this amount is ideal for optimizing muscle growth, assuming that adequate carbohydrate and fat is consumed in order to meet energy requirements. I see no need to go beyond this amount and at times have even questioned the validity of 2 grams. Obviously, there are instances in which a bodybuilder will need to consume more than the standard 1-2 grams per pound, such as during pre-contest prep, when carbs & fats have been reduced in an effort to shed bodyfat, but during the off-season, when muscle growth is the objective, I have yet to see a bodybuilder experience measurably greater growth when venturing beyond this pre-determined amount.

The take home message here is that there is no clinical evidence to suggest that protein consumption beyond the standard range supplies additional muscle building benefits, but we do know that the kidneys are responsible for processing protein, with larger amounts increasing the work-load on the kidneys. In those with normal kidney function, excess protein consumption does not appear to contribute to a decline in kidney function, likely because the stress generated by a high protein diet alone is not great enough to produce such an effect. However, in combination with other risk factors, very high protein diets (above 1-2 grams/pound) are associated with a worsening of kidney function. Therefore, it does not make any sense to follow a potentially injurious diet in the absence of documented benefits.

Excess protein is not the only dietary consideration in the management of high blood pressure. Sodium also plays a role. Unlike anabolic steroids, which indirectly increase sodium retention as a consequence of use, we have no excuse for ignorance when it comes to the deliberate consumption of excess sodium. This is something that is easily within our control and while not all pre-made foods list sodium content on their packaging, as a bodybuilder you shouldn’t be eating many of these foods anyway. When attempting to manipulate sodium to our advantage, there are 2 primary factors we need to concern ourselves with. They are total intake and consistency of intake. Most bodybuilders will require slightly more sodium than a sedentary individual of equal bodyweight, due to the sodium loss that occurs during training via perspiration. Those bodybuilders who work in hot environments and/or have manual labor jobs will need to make further adjustments according to need.

The body is constantly regulating sodium levels in order to maintain/establish homeostasis (balance), as the proper balance of electrolytes is critical for the preservation of life. Aldosterone, a anabolic steroids hormone produced by the adrenal glands, plays a key role in maintaining this balance through the regulation of sodium levels within the body. When sodium levels are low aldosterone levels increase, causing the body to excrete less sodium. When sodium levels are high, aldosterone levels decrease, causing the body to excrete more sodium. The body is in a constant state of evaluation, with even the slightest changes in sodium levels initiating a change in aldosterone concentration.

By maintaining a fairly consistent sodium intake, the body is only required to make subtle adjustments in order to maintain homeostasis, but when it is exposed to large fluctuations in sodium due to an ever-changing diet, aldosterone concentrations are altered dramatically. This can cause substantial increases in water retention and as a consequence, significant elevations in blood pressure. Therefore, a bodybuilder would likely be better off consistently consuming slightly more sodium than needed, rather than eating low sodium on most days, but high sodium on others. In some cases it can take the body several days to restore proper water balance after a sodium splurge, during which times blood pressure can remain elevated.

Another risk factor associated with kidney disease/failure, and which is heavily connected to the first, is the unwillingness to go off anabolic steroids for a prolonged period of time. Fearing the loss of muscle tissue, many of today’s bodybuilders remain on anabolic steroids 365 days a year. Now, most of the side effects associated with anabolic steroids use are transient, and kidney stress is no exception (in most cases), but when these stressors remain in place indefinitely, the affected organ(s) never get a chance to rest. For those who have already entered into Stage 1 kidney failure or worse, this has potentially dire ramifications, as the body never has a chance to normalize itself and may be pushed into later stages of kidney failure. Needless to say, a little prudence in matters such as this can go a long way in making a positive impact on one’s health.

Finally, dehydration can have a negative effect on kidney function by reducing blood flow to the kidneys. As a result, the kidneys are unable to properly remove toxins from the bloodstream, resulting in toxin build-up; a condition known as azotaemia. The kidneys require adequate blood flow in order to perform their job properly and nothing reduces blood flow more quickly than dehydration (aside from extensive blood loss). In fact, if water is completely withheld, death can result in as little as 2-3 days.

Kidney damage is not uncommon among pre-contest bodybuilders who frequently utilize diuretics in an effort to present a dry appearance onstage. Due to the potent nature of these drugs, one can simulate a state of severe water deprivation within days and in some cases mere hours. With protracted and/or repeated use, and depending on the dose administered, kidney damage can and often does occur to varying degrees.

Regardless of the cause(s), high blood pressure leading to kidney damage is a very real concern among anabolic steroid-using bodybuilders. The relative scarcity of outwardly discernible symptoms has earned it the moniker “the silent killer”, as many of those afflicted with the condition are unaware of its existence. This makes it potentially more dangerous than many other side effects, which manifest themselves openly.

As mentioned above, excessive protein & sodium intake, the use of NSAID’s, inadequate water consumption, and a refusal to take periodic breaks from anabolic steroid use, all serve to further compound the problem. With most bodybuilders being exposed to one or more of these risk factors, it makes sense to take steps to minimize their deleterious effects on the body, especially in those who individuals who have already entered into the beginning stages of kidney failure.

Supplementation is also a viable option in the prevention of kidney disease/failure. One of the most common classes of kidney support supplements are those which help reduce blood pressure. Fortunately, there are several clinically validated OTC supplements which have proven effective in the alleviation of this malady. Hawethorn berry is one of the most heavily researched of the bunch and at optimal dosage is quite effective at reducing blood pressure. Co-Q10, as well as celery seed extract, have also been shown to provide considerable benefit in this area. Other classes of supplementation include detoxifiers, antioxidants, and alkalinizers, as well as single compounds, such as vitamin B-6 and L-Carnitine, although not all of these products may be beneficial in every case. Underlying causes, as well as disease progression, should be taken into consideration when designing a kidneys support program.

Without doubt, ignorance is the #1 cause of kidney dysfunction in drug-using bodybuilders today. Often, it doesn’t take more than a few simple adjustments to mitigate further damage and bring things under control. I encourage all bodybuilders to regularly evaluate their kidney health through physician monitored bloodwork, as the kidneys do not possess the same self-rejuvenating capabilities as the liver. Once damage is sustained, it is oftentimes permanent. Therefore, preventative action is a must.

Friday, June 20, 2014

How to cycle Clen and Clen Side Effects and Doses



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. 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

  • Nausea
  • Nervousness 
  • Dizziness
  • Drowsiness 
  • Dry mouth
  • Facial flushing
  • Headache
  • Heartburn
  • Increased blood pressure
  • Increased sweating
  • Insomnia
  • Lightheadness
  • Muscle cramps
  • Tremors
  • Vomiting
  • Chest 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.

Post-Cycle Therapy: Clenbuterol 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 Clenbuterol, 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 Clenbuterol.

Clenbuterol has mild steroid-like properties and can be used by non anabolic steroids 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.

Is Clen for you?
The same precautions that apply to Ephedrine must be applied to Clenbuterol, although some people find ECA stacks harsher than Clenbuterol. 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.

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: 20mcg
Day2: 40mcg
Day3: 60mcg
Day4: 80mcg
Day5: 80mcg(Note: Increase the dose only when the side effects are tolerable)
Day6-Day12: 100mcg
Day13: 80mcg (Tapering is not necessary, but it helps some users get back to normal gradually)
Day14: 60mcg
Day15: off
Day16: off
Day 17: ECA/ NYC stack

Example of a second cycle:
Day1: 60mcg
Day2: 80mcg
Day3: 80mcg
Day4: 100mcg
Day5: 100mcg
Day6-Day12: 120mcg
Day13: 100mcg
Day14: 80mcg
Day15: off
Day16: off
Day 17: ECA/ NYC stack

Do not take Clenbuterol Past 4pm and drink plenty of water: 1.5-2 gallons a day.
All brands are not equal when it comes to Clenbuterol, different brands will yield different results. That about covers everything.

Thursday, June 5, 2014

GP Oxan (Anavar) by Geneza Pharmaceuticals


GP Oxan by Geneza Pharmaceuticals is an oral steroid which contains 10mg of the hormone Oxandrolone. This steroid is commonly called Anavar, or "Var" for short.

Anavar is considered one of the mildest steroids that there is. It is mildly anabolic and mildly androgenic. Even though it is a C-17 oral, it still has minimal effect on liver values even at higher doses. Var also isn’t known by bodybuilders as the steroid for big mass gains. Rather, the mass that is gained by GP Oxan will be quality gains, and gains that likely to be kept after the steroid is no longer being used. Users of Anavar often note a very good increase in strength. Some bodybuilders compare the strength increases seen by its use to be similar to GP Oxy on a mg for mg basis, but without the extra side effects! Because of this, and the fact that users won’t gain a lot of weight because of the drug, Var is a very popular drug for powerlifters and sports related athletes.

Due to its extremely mild nature, Var is also one of the most popular steroids amongst women bodybuilders. Anavar has also been shown in studies to actually decrease bodyfat during use, making it a great choice for bodybuilders who are in the cutting phase of their training.

GP Oxan is also very mild when it comes to shutting down the body’s ability to produce testosterone, making it a great choice for those looking to "bridge" between cycles while allowing the body to recover. Those looking to stack Anavar with something may chose a low dose of a testosterone to do with it. Also, the classic Anavar / Primo cycle is one of the most popular cutting cycles ever. This cycle provides one with quality muscle gain and minimal side effects and risk.

Clearly, GP Oxan is a great all around steroid. Male bodybuilders will typically use Anavar in doses of 50-100mg a day for 6-12wks. Var has a relatively short half life of about 8 hours. So one may chose to split dosages throughout the day in order to keep blood levels as stable as possible. Women bodybuilders typically find a dosage of 2.5-10mgs to be effective for promoting muscle gains and strength without the great risk of side effects.

Friday, May 30, 2014

Stanozolol by Accordo RX and muscular development


Pharmacology is the study of drugs and their effects. Anabolic pharmacology is the study of drugs that have a growth-promoting effect in muscle. This article will explore anabolic pharmacology by profiling a different anabolic drug and its effects each month. The focus of discussion this month will be the anabolic androgenic steroid, Stanozolol.

Stanozolol is a highly-modified synthetic version of dihydrotestosterone (DHT) that was originally sold under the trade name Winstrol. As you can see, there is an additional ring system attached to the traditional A-ring of the anabolic steroid structure. The binding data for Stanozolol shows it to have very poor binding for the androgen receptor. However, the half-life of nine hours for this anabolic steroid is quite long— making up for the lower affinity. Stanozolol is incapable of being converted to estrogenic metabolites through aromatization, and is already 5-alpha reduced, so it cannot be reduced further— but does seem to have some anti-aromatase activity.

Stanozolol has minimal binding to sex hormone-binding globulin (SHBG), so it circulates for the most part in the ‘free’ state. It has been shown that although stanozolol does not interact directly with the glucocorticoid receptor, it does interact with two glucocorticoid-binding proteins known as STBP and LAGS. This interaction ‘bumps off’ bound cortisol into free circulation. At the same time, Stanozolol has been shown to interfere with cortisol release from the adrenal gland. This results in reduced cortisol levels, with chronic usage. In fact, many people notice severe joint pain when using Stanozolol, especially when used alone. This can result in a rebound effect in cortisol production when going off Stanozolol.

 Even though Stanozolol has a very large anabolic-to-androgenic ratio, it is quite androgenic. The anti-glucocorticoid effect of this drug likely augments its anabolic/androgenic ratio beyond that of its androgen receptor-binding effects alone. Stanozolol decreases thyroxine-binding globulin (TBG) levels but not as much as some of the other common anabolic-androgenic steroids.

 In addition to tablets for oral administration, Stanozolol is available as water-based suspension for injection. Because it is not esterified, this steroid needs to be injected every day. Also, water-based injections are a lot more prone to bacterial contamination, so more care is needed to keep a multi-use bottle sterile. The relatively large crystal size of some preparations limits the size of needle that can be used, because the crystals will jam smaller needles. There are some formulations available that have smaller crystal size; however, these seem to have a shorter half-life— most likely due to the crystals dispersing faster within the muscle.

Because Stanozolol is C-17 alpha-alkylated, it has the potential for liver toxicity— but this is somewhat reduced with the injectable form because a lower overall dose is often used. Stanozolol has a favorable anabolic-to-androgenic ratio, but most do not consider it to be very effective. This is largely due to the fact that Stanozolol does not result in large water weight gains.

Friday, May 23, 2014

Proviron (mesterolone) by Jintani Labs


Proviron (mesterolone) is oral androgen mesterolone (1-methyl dihydrotestosterone). Similar to dihydrotestosterone, mesterolone is a strong androgen with only a weak level of anabolic activity.This is due to the fact that like dihydrotestosterone, mesterolone is rapidly reduced to inactive diol metabolites in muscle tissue where concentrations of the 3-hydroxysteroid dehydrogenase enzyme are high. The belief that the weak anabolic nature of this compound indicates a tendency to block the androgen receptor in muscle tissue, thereby reducing the gains of other more potent muscle-building steroids, should likewise not be taken seriously. In fact, due to its extremely high affinity for plasma binding proteins such as SHBG, mesterolone may actually work to potentate the activity of other steroids by displacing a higher percentage into a free, unbound state. Among athletes, mesterolone is primarily used to increase androgen levels when dieting or preparing for a contest, and as an antiestrogen due to its intrinsic ability to antagonize the aromatase enzyme.

Mesterolone is a modified form of dihydrotestosterone. It differs by the addition of a methyl group at carbon, which helps protect the hormone from hepatic metabolism during oral administration. The same structural modification is also used with oral Primobolan (methenolone) tablets. Alkylation at the one position slows hepatic metabolism of the steroid during the first pass, although much less profoundly than c-17 alpha alkylation. Mesterolone is resistant enough to breakdown to allow therapeutically beneficial blood levels to be achieved, although the overall bioavailability remains much lower than c-17 alpha alkylated oral steroids. Mesterolone also has a very strong binding affinity for Sex Hormone Binding Globulin/1o This may act to displace other steroids more weakly bound to SHBG into a free (active) state.

Mesterolone is not aromatized by the body, and is not measurably estrogenic. An anti-estrogen is not necessary when using this steroid, as the drug is unlikely to induce gynecomastia, water retention, or other estrogen-related side effects. Mesterolone is actually believed to act as an antiaromatase in the body, preventing or slowing the conversion of steroids into estrogen.

The result is somewhat comparable to Arimidex, although less profound. The anti-estrogenic properties of mesterolone are not unique, and a number of other steroids have demonstrated similar activity. Dihydrotestosterone and Masteron (2-methyl-dihydrotestosterone), for example, have been successfully used as therapies for gynecomastia and breast cancer due to their strong androgenic and potentially anti-estrogenic effect. It has also been suggested that nandrolone may even lower aromatase activity in peripheral tissues where it is more resistant to estrogen conversion (the most active site of nandrolone aromatization seems to be the liver).The antiestrogenic effect of all of these compounds is presumably caused by their ability to compete with other substrates for binding to the aromatase enzyme. With the aromatase enzyme bound to the steroid, yet being unable to alter it, an inhibiting effect is achieved as it is temporarily blocked from interacting with other hormones.

Mesterolone is classified as an androgenic steroid. Androgenic side effects are common with this substance, especially with higher doses. This may include bouts of oily skin, acne, and body/facial hair growth. Anabolic/androgenic steroids may also aggravate male pattern hair loss. Women are also warned of the potential virilizing effects of anabolic steroids. These may include a deepening of the voice, menstrual irregularities, changes in skin texture, facial hair growth, and clitoral enlargement. Additionally, the 5-alpha reductase enzyme does not metabolize mesterolone, so its relative androgenicity is not affected by finasteride.

Mesterolone is not c17-alpha alkylated, and not known to produce hepatotoxic effects; liver toxicity is unlikely.

Anabolic/androgenic steroids can have deleterious effects on serum cholesterol. This includes a tendency to reduce HDL (good) cholesterol values and increase LDL (bad) cholesterol values, which may shift the HDL to LDL balance in a direction that favors greater risk of arteriosclerosis. The relative impact of an anabolic/androgenic steroid on serum lipids is dependant on the dose, route of administration (oral vs. injectable), type of steroid (aromatizable or non-aromatizable), and level of resistance to hepatic metabolism. Mesterolone is an oral non-aromatizable androgen,and expected to have a notable negative effect on lipids. Studies administering 100 mg of mesterolone per day to hypogonadal men for approximately 6 months demonstrated a significant increase in total cholesterol (18.80/0) and LDL cholesterol (65.20/0), accompanied by a significant decrease in HDL cholesterol (-35.7°;6).

Mesterolone should not be used when cardiovascular risk factors preclude the use of other oral steroids. To help reduce cardiovascular strain it is advised to maintain an active cardiovascular exercise program and minimize the intake of saturated fats, cholesterol, and simple carbohydrates at all times during active anabolic steroids administration. Supplementing with fish oils (4 grams per day) and a natural cholesterol/antioxidant formula such as Lipid Stabil or a product with comparable ingredients is also recommended.

To treat androgen insufficiency, mesterolone is usually given in a dose of 1 tablet (25 mg) three times per day at the initiation of therapy. The drug is later continued at a lower maintenance dose, which usually consists of taking 1 tablet (25 mg) one to two times per day. Similar doses are used to support male fertility, usually in conjunction with other fertility drugs like injectable FSH. The usual dosage among male athletes is between 50 mg and 150 mg of mesterolone per day, or two to six 25 mg tablets. The drug is typically taken in cycles of 6-12 weeks in length, which is usually a sufficient period of time to notice the benefits of drug therapy. Many bodybuilders favor the use of mesterolone during dieting phases or contest preparation, when low estrogen and high androgen levels are particularly desirable. This is especially beneficial when anabolics like Winstrol, Anavar, or Primobolan are being used alone, as the androgenic content of these drugs is relatively low.

Mesterolone can be effectively used here to adjust the androgen to estrogen ratio upwards, bringing about an increase in the hardness and density of the muscles, supporting libido and general sense of well being, and increasing the tendency to burn body fat. It is also commonly used (at a similar dosage) to prevent gynecomastia when other aromatizable steroids are being administered, often in conjunction with 10-20 mg
per day of Nolvadex.

Mesterolone is not approved for use in women.This agent is not recommended for women for physique- or performance-enhancing purposes due to its strong androgenic nature and tendency to produce virilizing side
effects. Some women do favor the drug, however, and find a single 25 mg tablet enough to efficiently shift the hormone balance in the body, greatly impacting the look of definition to the physique. Intake is usually limited to no longer than four or five weeks in such situations to minimize the chance of developing lasting virilizing effects. One tablet used in conjunction with 10 or 20 mg of Nolvadex can be even more efficient for muscle hardening, creating an environment where the body is much more inclined to burn off extra body fat, especially in female trouble areas like the hips and thighs. Extreme caution should be taken with such use, however.

Friday, May 2, 2014

Anabolic Steroids and Side Effects


Anabolic steroids tend to have side effects, especially when used at above therapeutic dosages. They can increase cholesterol, raise the hematocrit ("thickening" the blood), suppress natural testosterone production, and at least for oral varieties, impair liver function. Let's not forget, too, those pesky cosmetic issues like acne, accelerated male pattern hair loss, and gynecomastia. Both sides of the anabolic steroid argument readily agree on this. Where there seems to be much disagreement, however, are the long-term risks of anabolic steroid use. Are anabolic steroid-related side effects reversible and if so, does a career of anabolic steroid use still increase the likelihood of disease or death later on? While science has yet to answer the latter question, the former has been the subject of much investigation.

Before we get into the specific results, I think it is important to examine the protocols of the study. A total of 32 men participated in this investigation, each identified as a bodybuilder or powerlifter. About half of the men (15) were former anabolic steroid abusers, with an average age of 38. The amount of time since the men quit taking the drugs varied from one to 10 years, with an average of about 3.5 years. While they were using steroids, their average intake was 720 milligrams per week for 26 weeks per year over nine years. The other 17 men were current anabolic steroid abusers, with an average age of 30. They used an average of 750 milligrams per week for approximately 32 weeks per year over an eight-year period. The two groups in this study were fairly well balanced as far as history and usage patterns go, and seem to represent a formidable though fairly average history of anabolic steroid use at above therapeutic levels.

While they were using anabolic steroid, each of the subjects self-administered without a medical prescription. According to a questionnaire filled out by the subjects, the most popular injectable agents of use were Boldenone, Drostanolone, Methenolone, Nandrolone, Stanozolol and various esters of testosterone such as Testosterone enanthate and Sustanon 250. The orals most widely used included 4-chlorodehydromethyltestosterone (Oral Turinabol),  Mesterolone, Methenolone, Methandrostenolone, Oxymetholone, Oxandrolone and Stanozolol. Five ex-abusers and six current abusers had occasionally used human growth hormone (hGH) as part of their programs, at a dosage between 2 and 16 IU daily. Other non-steroid drugs commonly used by both groups included anti-estrogens and clenbuterol, as would be expected in such populations.

Now let's get to the results. To begin with, current steroid users noticed a predictable (negative) shift in cholesterol levels. In particular, HDL (good) cholesterol values were very low (< .9 nmol/L) in 15 out of 17 current anabolic steroid abusers. The cholesterol balance, of course, may reflect the ongoing disposition of plaque in the arteries during use. As such, a higher HDL level and HDL/ LDL ratio are more desirable. After a minimum of one year of abstinence, the HDL level was below the normal range in only one ex-abuser. These results are in line with other short-term administration studies, as well as the common understanding of anabolic steroid, demonstrating a strong negative impact on serum cholesterol levels, and by extension cardiovascular disease risk, during the misuse of anabolic steroids. However, they also appear to support the reversibility of anabolic steroid-related changes in serum lipids, as no consistent (negative) findings were carried over into the lab results of ex-abusers.

There were also distinct changes in the blood cell counts of current anabolic steroid users. In particular, there was a significant increase in hemoglobin (5%) and hematocrit (9%). These changes may reflect an increase in the oxygen-carrying capacity of the blood, and could improve performance. However, they may also represent an unwanted "thickening" of the blood by nature of increased red cell concentrations. This is very important because it can increase the likelihood of a cardiovascular event such as heart attack or stroke— especially in light of the other common health marker changes during anabolic steroid use, such as impaired cholesterol and elevated blood pressure. In the group of former steroid users, these changes in blood cell counts were not noticed. These findings support the position that there are distinct side effects on red blood cell counts during steroid use, but these changes are reversible when the drugs are discontinued.

In the area of liver enzymes, there were notable changes in both groups. All of the current steroid users except one had elevated AST (aspartate transaminase) and ALT (alanine transaminase) values, which is often indicative of hepatic strain due to c-17 alpha alkylated (oral) anabolic steroid use. AST and ALT enzymes were elevated above normal in three and six of the former steroid abusers, respectively. The researchers discussed the potential elevation of liver enzyme values caused by exercise, and noted that both groups practiced strength training. However, changes in enzymes not related to exercise (such as GLDH) suggested the strain in current users was anabolic steroid-related. There were no signs of lasting impairment of the organ in either group upon ultrasound examination. These results are in line with numerous previous studies that show a risk of liver toxicity with current anabolic steroid misuse. However, they do not support the position that anabolic steroid misuse increases the long-term (post-administration) likelihood of hepatic health issues.

Testosterone levels were exceedingly high in steroid abusers, owing to the prominence of synthetic testosterone use in this group (the source was not natural but exogenous). This was accompanied by a severe suppression of gonadotropin levels, with LH and FSH levels lower by 91-94 %. This reflects the underlying suppression of natural testosterone production in current steroid abusers. Unlike most of the other health markers, serum testosterone did not seem to recover to normal levels after anabolic steroid misuse. A troubling 13 of the former steroid abusers had testosterone levels that measured in the lowest 20 % of the normal range for men. Two of the subjects had testosterone that measured below normal. The other hormones were within reference ranges for this group. While we generally like to view testosterone suppression during anabolic steroid use as a temporary side effect, it may not always be. If the results of this study hold true for the general population, it suggests that former steroid users are likely to struggle with sub-optimal testosterone production years after stopping use of the drugs. Therefore, this part of the study did provide distinct evidence of prolonged steroid-related side effects.

There were some other areas of effect to note during this study. For example, there was an increase in thrombocytes in current steroid abusers compared to ex-abusers. Thrombocytes are cells involved in blood clotting. Together with increased hematocrit and possibly blood pressure, this could increase the likelihood of serious adverse cardiovascular events such as blood clot or stroke. While still relatively rare, we have seen occasional reports of such in otherwise healthy anabolic steroid users. With regard to other common blood markers, there were no significant differences between groups in serum electrolytes (sodium, potassium, magnesium, calcium), iron, urea, creatinine, uric acid, glucose or HBA1. Lastly, while the researchers did not chart common cosmetic issues, they did report a high prevalence of gynecomastia in both groups (approximately two-thirds of subjects had or are currently dealing with it). Gynecomastia can be a permanent side effect of anabolic steroid misuse that requires surgery for correction. There are no surprises here.

In the context of this study, most of the short-term negative health effects of anabolic steroid misuse appeared to be reversible. In particular, former steroid users did not have the same unfavorable changes in red or white blood cell counts, serum cholesterol levels or liver enzyme values noted in current anabolic steroid users. The immediate effects of anabolic steroid on cardiovascular and liver health markers, which we know can be markedly negative, appear to go away after the drugs have been discontinued. These results do lend support for the acute safety of these drugs. They also mirror what we've seen in many short-term administration studies, which we touched on earlier in this piece. In this case, we are simply looking more broadly (and in a real-world context) at populations of users and former users for these same changes.

The reversibility of changes to basic health markers, of course, does not necessarily discount that there were changes in the first place. Disturbed health markers, even in the short term, could reflect underlying damage to our health. There is still much question as to whether a substantial period of anabolic steroid misuse could lead to a greater incidence of disease or death years later. For example, elevated cholesterol and LDL/HDL ratio are associated with heart-disease-promoting changes in the cardiovascular system. Logically speaking, one might still be contributing to atherosclerosis (hardening of the arteries) during non-prescribed anabolic steroid administration, even if these health markers return to normal after. This is an area of medicine that needs much greater examination, of course. As mentioned in the opening of this article, such studies are lacking.

In the area of hormonal health, there does appear to be a valid reason for concern if you are contemplating the use of anabolic steroids. In the men of this study, a history of anabolic steroid misuse was associated with insufficient testosterone levels long after stopping. Low testosterone may cause immediate issues such as energy loss, impaired mental focus, reduced libido, and loss of strength and muscle mass. In the long term, however, more serious issues such as heart disease, diabetes and cancer have been linked to male hormone deficiency. It is conceivable that a "minor" problem with a low or even low-end-of-normal testosterone level after steroid use could foster considerable health issues later in life if not corrected. "Low T" is certainly a growing concern for aging men in clinical medicine. Therefore, one should consider both the positive and negative findings of this study before placing any weight on the results, one way or the other. As always, be safe.

Thursday, April 24, 2014

Boldenone Undecylenate - Equipoise


Equipoise is the popularly referenced brand name for the veterinary injectable steroid boldenone undecylenate. Specifically it is a derivative of testosterone, which exhibits strong anabolic and moderately androgenic properties. The boldenone undecylenate ester greatly extends the activity of the drug (the undecylenate ester is only one carbon atom longer than decanoate), so that clinically injections would need to be repeated every three or four weeks. In veterinary medicine Equipoise is most commonly used on horses, exhibiting a pronounced effect on lean bodyweight, appetite and general disposition of the animal. This compound is also said to shows a marked ability for increasing red blood cell production, although there should be no confusion that this is an effect characteristic of newly all anabolic/androgenic steroids. The favorable properties of this drug are greatly appreciated by athletes, Equipoise being a very popular injectable in recent years. It is considered by many to be a stronger, slightly more androgenic Deca-Durabolin. It is generally cheaper, and could replace Deca in most cycles without greatly changing the end result.

The side effects associated with Equipoise are generally mild. The structure of boldenone undecylenate does allow it to convert into estrogen, but it does not have an extremely high affinity to do so. To try and quantify this we can look toward aromatization studies, which suggest that its rate of estrogen conversion should be roughly half that of testosterone's. The tendency to develop a noticeable amount of water retention with this drug would therefore be slightly higher than that with Deca-Durabolin (with an estimated 20% conversion), but much less than what would be expected with a stronger agent such as Testosterone. While one does still have a chance of encountering an estrogen related side effect as such when using this substance, it is not a common problem when taken at a moderate dosage level. Gynecomastia might theoretically become a concern, but is usually only heaved of with very sensitive individuals or (again) those venturing high in dosage. Should estrogenic effects become troublesome, the addition of Nolvadex and/or Proviron should of course make the cycle more tolerable. An antiaromatase such as  Arimidex would be stronger options, however probably not indicated with a mild drug as such.

Although it stays active for a much longer time, Equipoise is injected at least once per week by athletes. It is most commonly used at a dosage of 200-400mg (4-8 ml, 50mg version) per week for men, 50-75 mg per week for women. Should a 25mg version be the only product available, the injection volume can become quite uncomfortable. The dosage schedule can be further divided, perhaps injections given every other day to reduce discomfort. One should also take caution to rotate injection sites regularly, so as to avoid irritation or infection. Should too large an oil volume be injected into one site, an abscess may form that requires surgical draining. To avoid such a problem, athletes will usually limit each injection to 3ml and reuse each site no more than once per week, preferably every other week. With Equipoise this may require using not only the gluteus, but also the outer thighs for an injection site. Of course all problems associated with 25mg and 50mg dosed products are eliminated with the newer 100 mg and 200mg/ml versions of this steroid, which clearly give the user much more dosage freedom and injection comfort.

Thursday, April 17, 2014

Deca Durabolin: Miracle or Monster? Nandrolone decanoate Dosages


Deca Durabolin has a long history of use in the athletic community and remains, to this day, to be one of the most popular anabolic steroids in the sport's world. The popularity it enjoys stems from the fact that it has a very high anabolic activity and produces significant mass increases with relatively few side effects. It also produces less water retention, has less effect on blood pressure and is far less toxic to the liver and kidneys than most of its mass-building buddies.

Another interesting quality of Deca Durabolin is that is helps alleviate the pain of sore joints. Some speculate that it exerts this effect by occupying the same anti-inflammatory receptors that cortisol does. In doing so, it displaces the more catabolic cortisol and replaces it with an anabolic analogue that has similar anti-inflammatory properties. While this sounds like a miracle for athletes with connective tissue problems and moderate to severe joint pain, there's some data to suggest that it might also be the root of some chronic degenerative changes that occur in the joint later in life.

Of course it would be misleading to present Deca Durabolin as a drug completely devoid of side effects. When dosages go beyond 400-600mg/week sensitive individuals may see an increase in blood pressure, prolonged bleeding time of cuts, increased oil production by the sebaceous gland (leading to acne breakouts), increased hostility, increased sex drive and a fall in sperm production. If blood pressure increases too much, headaches can become more frequent. Oh, and of course we can't overlook the fact that long-term use of this drug by male athletes can lead to impotence (which is the exact opposite of the increased sex drive experienced when dosages are kept within limits and for acceptable durations of time). The dreaded "Deca Dick" (as it has become widely known) doesn't seem to affect users that are combining Deca with another more androgenic compound such as testosterone, trenbolone, or dianabol.

As for the female user, women can usually get away with a dose of up to 50mg/week without any major problems. However, virilization (masculinizing side effects) is always a concern when women use any anabolic hormone. While each individual user has differing sensitivities and side effects , common problems include deepening of the voice, increased body and facial hair, increased acne breakouts, and clitoral hypertrophy.

As with all steroids, diet is very important for effectiveness to be maximized. Protein intake should be high, as should overall calorie intake if significant mass gains are to be experienced.

Recommened dosages:

Deca Durabolin is commonly used in the range of 200 - 600 mg/week. Injecting more than 600mg/week is not advised. Despite this fact, there are many reports of bodybuilders taking as much as 1000mg/ week. In the case of Deca Durabolin, more is not necessarily better.

Most male athletes experience good results with dosages as low as 400mg/week. If large gains in muscle mass are the primary goal then stacking Deca with drugs such as Dianabol and Testosterone is not uncommon.

For female athletes 25-50mg/week is the commonly used dose and this is often combined with Winstrol, Anavar, or Primobolan tablets. Dosages over 100mg are not advised.

In conclusion, Deca Durabolin is often used where problems with testosterone use have been encountered. It is less prone to aromatization and is deemed to produce an overall sense of well being. One final warning; for those intending to participate in sports that drug-test their athletes, it's important to understand that Deca Durabolin metabolites can last in the body for up to 18 months (and possibly longer depending on bodyfat levels during use) which can easily result in a failed drug test for upwards of a year and a half after the final injection

Friday, April 11, 2014

Proviron (mesterolone)


Proviron is an oral DHT steroid compound similar to Masteron. Although it is not an ideal compound for building muscle (actually it is not good at all for this purpose), Proviron is helpful in stacks because of its unique ability to keep the body from turning testosterone into estrogen, thus giving the testosterone a better anabolic effect. This aids the bodybuilder in many ways. First, it helps reduce estrogenic side effects of other steroids water-retention, lowered sex drive, gynocomastia, etc. Also, Proviron can help boost the potency of testosterone in the body by freeing testosterone from its binding to sex hormone-binding globulin.

Proviron is therefore best stacked with testosterone, which makes taking anti-estrogen compounds unnecessary. However, Proviron can cause high blood pressure so blood pressure medication may be required for those prone to hypertension.

Proviron is the Schering brand name for the oral androgen mesterolone (1 methyl-dihydrotestosterone). Just as with DHT, the activity of this steroid is that of a strong androgen which does not aromatize into estrogen. In clinical situations Proviron is generally used to treat various types of sexual dysfunction, which often result from a low endogenous testosterone level. It can usually reverse problems of sexual disinterest and impotency, and is sometimes used to increase the sperm count. Proviron does not stimulate the body to produce testosterone, but is simply an oral androgen substitute that is used to compensate for a lack of the natural male androgen.

Although Proviron is strongly androgenic, the anabolic effect of it is considered too weak for muscle building purposes. This is due to the fact that Proviron is rapidly reduced to inactive metabolites in muscle tissue, a trait also characteristic of dihydrotestosterone. The belief that the weak anabolic nature of this compound indicated a tendency to block the androgen receptor in muscle tissue, thereby reducing the gains of other more potent muscle building steroids, should likewise not be taken seriously. In fact due to its extremely high affinity for plasma binding proteins such as sex hormone-binding globulin, Proviron may actually work to increase the activity of other steroids by displacing a higher percentage into a free, unbound state. Among athletes Proviron is primarily used as an anti-estrogen. It is believed to act as an anti-aromatase in the body, preventing or slowing the conversion of steroids into estrogen. The result is somewhat comparable to Arimidex (though less profound), the drug acting to prevent the buildup of estrogen in the body. This is in direct contrast to Nolvadex, which only blocks the ability of estrogen to bind and activate receptors in certain tissues. The anti-aromatization effect is preferred, as it is a more direct and efficient means of dealing with the problem of estrogenic side effects. Another disadvantage of Nolvadex is that if discontinued too early, a rebound effect may occur as high serum estrogen levels are again free to take action. This of course could mean a rapid onset of side effects such as gynecomastia. Most actually prefer to use both Proviron and Nolvadex, especially during strongly estrogenic cycles. With each item attacking estrogen at a different angle, side effects are often greatly reduced.

The anti-estrogenic properties of Proviron are not unique to this compound. A number of steroids have in fact demonstrated similar activity. Dihydrotestosterone and Masteron (2methyl-dihydrotestosterone) for example have been successfully used as therapies for gynecomastia and breast cancer due to their strong anti-estrogenic effect. It has been suggested that nandrolone may even lower aromatase activity in peripheral tissues where it is more resistant to estrogen conversion (the most active site of nandrolone aromatization seems to be the liver). The anti-estrogenic effect of all of these compounds is presumably caused by their ability to compete with other substrates for binding to the aromatase enzyme. With the aromatase enzyme bound to the steroid, yet being unable to alter it, and inhibiting effect is achieved as it is temporarily blocked from interacting with other hormones.

Proviron is also favored by many during contest preparations, when a lower estrogen/high androgen level is particularly sought after. This is especially beneficial when anabolics like Winstrol, oxandrolone and Primobolan are being used alone, as the androgenic content of these drugs is relatively low. Proviron can supplement a well needed androgen, and bring about an increase in the hardness and density of the muscles. Women in particular find a single 25mg tablet will efficiently shift the androgen/estrogen ratio, and can have a great impact on the physique. Since this is such a strong androgen however, extreme caution should be taken with administration. Higher dosages clearly have the potential to cause virilization symptoms quite readily. For this reason females will rarely take more than one tablet per day, and limit the length of intake to no longer than four or five weeks. One tablet used in conjunction with 10 or 20mg of Nolvadex can be even more efficient for muscle hardening, creating an environment where the body is much more inclined to burn off extra body fat (especially in female trouble areas like the hips and thighs).

The typical dosage for men is one to four 25 mg per tablets per day. This is a sufficient amount to prevent gynecomastia, Proviron is often used throughout the entire cycle. As mentioned earlier, it is often combined with Nolvadex (tamoxifen citrate) or Clomid (clomiphene citrate) when heavily estrogenic steroids are being taken (Dianabol, testosterone etc.). Administering 50mg of Proviron and 20mg Nolvadex daily has proven extremely effective in such instances, and it is quite uncommon for higher dosages to be required. And just as we discussed for women, the androgenic nature of this compound is greatly welcome during contest preparation. Here again Proviron should noticeably benefit the hardness and density of the muscle, while at the same time increasing the tendency to burn off a greater amount of body fat. Proviron is usually well tolerated and side effects (men) are rare with dosages under 100 mg per day. Above this, one may develop an excessively high androgen level and encounter some problems. Typical androgenic side effects include oily skin, acne, body/facial hair growth and exacerbation of a male pattern baldness condition, and may occur even with the use of a moderate dosage. With the strong effect DHT has on the reproductive system, androgenic actions may also include an extreme heightening of male libido. And as discussed earlier, Women should be careful around Proviron. It is an androgen, and as such has the potential to produce virilization symptoms quite readily. This includes, of course, a deepening of the voice, menstrual irregularities, changes in skin texture and clitoral enlargement.

Proviron is also not a c17 alpha alkylated compound, an alteration commonly used with oral anabolic steroids. Not using this structure in the case of Proviron removes the notable risk of liver toxicity we normally associate with oral drugs. It is therefore considered a “safe” oral, the user having no need to worry about serious complications with use. This steroid in fact utilizes the same 1-methylation we see present on Primobolan (methenolone), another well tolerated orally active compound. Alkylation at the one position also slows metabolism of the steroid during the first pass, although much less profoundly than 17 alpha alkylation. Likewise Proviron and Primobolan are resistant enough to breakdown to allow therapeutically beneficial blood levels to be achieved, although the overall bioavailability of these compounds is still much lower than methylated oral steroids.

The popularity of Proviron amongst bodybuilders has been increasing in recent years. Many experienced bodybuilders have in fact come to swear by it, incorporating it effectively in most markedly estrogenic cycles. Due to high demand Proviron is now very easy to obtain on the black market. Most versions will be manufactured by Schering, and should cost about $1-$2 per 25 mg tab. This drug is packaged in both push-through strips and small glass vials, so do not let this alarm you. There is currently no need to worry about authenticity with this drug, as no counterfeits are known to exist. If money and availability does not prevent it, Arimidex, Femara, or Aromasin ares actually a much better choice than Proviron though. These drugs were designed specifically as an anti-aromatase, and works much more effectively than anything else we have available.