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Cabergoline is a drug most often medically prescribed for its ability to inhibit prolactin secretion via its action as a dopamine agonist. Used in the treatment of such diseases as Parkinson's disease (1), acromegaly (2), restless leg syndrome (3), Cushing?s syndrome (4), hyperprolactinemia (5), among others, the drug has been adopted by bodybuilders and strength athletes as a means to combat prolactin related side effects caused by certain anabolic steroids. For this purpose cabergoline is extremely effective while presenting little risk in terms of serious side effects to the health of the user when used for this purpose.

Steroid users should be concerned about excessive prolactin levels because of the side effects associated with them. Prolactin is a naturally occurring hormone primarily produced by the lactotrophs located in the pituitary gland, with a minority amount of the hormone being produced by other tissues/cells of the body. Prolactin plays a major role in lactation in most mammals including humans. It both stimulates milk production as well as inducing lobuloalveolar growth of the mammary gland. Obviously both of these side effects would be of great concern to bodybuilders and strength athletes from both a health and cosmetic standpoint. Decreased sex drive, sperm production and sexual function may also be related to elevated levels of this hormone (6, 7). In fact even in men with regular healthy levels of prolactin cabergoline can help to temporarily reduce the amount of the hormone that is secreted which leads to such advantages as an increase sex drive, improvement in sexual function (quality of erection) as well as reducing the refractory period for users (the amount of time between erections) (8).

When we wrote the Underground Book Thailand had closed his borders for Steroids and Male enhancement pills, mostly counterfeited Viagra. Pfizer makes millions of profit, producing a sildenafil containing tablet costs only cents and they sold it for a hundred fold. Thailand also sold cheap generic tablets and many people where able to buy outside their regional healthsystem. We all know how strong the pharmaceutical lobby is. The uSA protects his taxpayers and the pressure on Thailand became so high that it gave in.

China in fact owns the USA (financially) and this proud country didn’t gave in, the bodybuilding community had acces to China’s big pharma. First they sold reliable Growth hormones (rhGH) the famous Jintropin and ruined the very high prices of the US and European Pharma’s asked for their products. China also sold cheap API’s (raw powders) and all the necessary ancillairies. Soon all kind of Underground Laboratories (UG Labs) some good most of them bad, and home brewers bought their products in China.

Increased T/E ratio in men

 

When testosterone levels are normal, and a man is experiencing signs of andropause, the hormonal culprit is usually estrogen (and chemicals that mimic the actions of estrogen), the female hormone. Both men and women have specific amounts of estrogen in their bodies. Young men may have a ratio of testosterone to estrogen of 50:1. The ratio drops to 20:1 or even as low as 8:1 with normal aging.

When estrogen levels in a man increase, the actions of testosterone are reduced. Even worse. While estrogens in women protect them from heart disease and osteoporosis, the effects are the opposite for men. Too much estrogen will actually increase the risk of heart attacks in men.

Unfortunately, this is exactly the set of problems that we are currently facing. A combina­tion of our lifestyle and dietary choices, stress, use of anabolic androgenic steroids, medications and/or alcohol coupled with the pervasive amounts of estrogenic pollutants found in plastics and our water supply are the reasons why estradiol levels are climbing in men. In fact, we now see men with estrogen levels higher than that of many women.  As estrogen rises in men, testosterone drop and mammary gland tissue begins to grow (creating male breasts). This problem is so common that male breast reduction is now the fastest growing surgery in America!

Nilevar (Norethandrolone)

This is supposedly one of the first steroids in circulation in bodybuilding circles. Its what Arthur Jones had Bill Pearl on in 1956, and it gave him a gain of 30 pounds to win the Universe that year. Not coincidentally 1956 was the release of Nilevar by Searle in the US. The same company that would later bring us Anavar (oxandrolone) which was a lot milder on the system and notably less toxic. Nilevar is rarely used these days.

One could state, though not technically correct, that the substrate is an oral Deca preparation. It stems from the same base steroid (nortestosterone) and acts in a very similar fashion. It too is a potent stimulator of the androgen receptor, substantiated by its readiness to cause virilization in female users. Its likewise deactivated by the 5-alpha-reductase, which explains why in lower end doses its actually one of the mildest steroids, androgenically, in men. Norethandrolone is also a noted progestin and also aromatizes at some rate. This means, very much like nandrolone, that it can cause estrogenic side-effects with small amounts of circulating estrogen thanks to the estrogen-agonizing properties of the progestagenic activity.

Unrealized Potential: Before Quadzilla, There was Jeff King!

It was still the era of Frank Zane, where the beauty if symmetry dominated over competitors possessing beastly mass. To those that felt uninspired by the beach-bodies in vogue, Casey Viator, Tim Belknap and Tom Platz were exalted as unredeemed heroes ¾ always placing well but forced to look on as the likes of Dickerson, Makkawy and Bannout pranced off with the big checks. It was almost as if the meek truly had inherited the Earth.

The connoisseurs of mass felt that nothing could be more inspirational than photos of Bertil grunting out inclines with 180-pound dumbbells or Plants tensing his ponderous thighs between sets. We thrilled to tales of the Barbarian Brothers; throwing Olympic plates like Frisbees, kicking each other in the face for last rep motivation. Although this type of hardcore attitude was downplayed so that "the sport could reach a wider audience," we were just waiting for another big man to reclaim the Olympia crown and, in so doing, bring our doctrines back into prominence.

 kfsdjhgdshjhhhaawwweeaaa aaaa Since the times of the first, ancient Olympics, since the dawn of sports people have been cheating. That was then and that is now. Anti-doping organizations and sports associations are constantly chasing dopers who resort to more radical means every time. The lengths to which these “athletes” go to get an advantage is sometimes shocking. They are literally putting their lives in danger by experimenting with non-clinically tested drugs.

This blog post is meant to give an insight in the newest doping products that are out there on the market and to show how hard it is to actually detect these. And how scientific progress is often misused by cheaters. The sources I used are all scientific and can be send upon request.

In 2008, Cell published an article which was looked on with interest by the world of sports. Professor Ron Evans of La Jolla, California was doing research to find a cure for the increasing epidemic of obesity and diabetes. He found a substance that would trick the cells in thinking they exercised a lot while in fact they had been mostly idle. The mice ran faste, had better endurance and burnt fat.

When the mice were actually following a training regime the results almost doubled. The media dubbed it the “coach-potato drug”, the miracle cure to obesity and diabetes for people who were unable to exercise.

The History of Synthetic Testosterone

Testosterone has long been banned in sports as a performance-enhancing drug. This use may soon be accepted in medicine alongside other legitimate hormonal therapies (by John M. Hoberman and Charles E. Yesalis )

On June 1, 1889, Charles Edouard Brown-Sequard, a prominent French physiologist, announced at the Societe de Biologie in Paris that he had devised a rejuvenating therapy for the body and mind. The 72-year-old professor reported that he had drastically reversed his own decline by injecting himself with a liquid extract derived from the testicles of dogs and guinea pigs. These injections, he told his audience, had increased his physical strength and intellectual energy, relieved his constipation and even lengthened the arc of his urine.

Almost all experts, including some of Brown-Sequard's contemporaries, have agreed that these positive effects were induced by the power of suggestion, despite Brown-Sequard's claims to the contrary. Yet he was correct in proposing that the functions of the testicles might be enhanced or restored by replacing the substances they produce. His achievement was thus to make the idea of the "internal secretion," initially proposed by another well-known French physiologist, Claude Bernard, in 1855, the basis of an organotherapeutic "replacement" technique. Brown-Sequard's insight that internal secretions could act as physiological regulators (named hormones in 1905) makes him one of the founders of modern endocrinology. So began an era of increasingly sophisticated hormonal treatments that led to the synthesis in 1935 of testosterone, the primary male hormone produced by the testicles.

How Bodybuilding Has Changed

Bodybuilding has changed--drastically! In fact, just about everything in bodybuilding has changed; from training, to diet, to supplementation, the sport that was once defined by beauty and aesthetics, is now defined by drugs and deformity.

 

So let's talk about what BODYBUILDING actually is. Is it an art? Is it a science? Is it a lifestyle? Is it a sport? Yes, it's actually all us these things, and much, much, more. Bodybuilding can be defined as the deliberate and methodical reconstruction of cells and tissues in the human body, in an attempt to maximize lean muscle mass while minimizing body fat levels. This is not an easy task at all, and requires an intimate and extensive understanding of biology, chemistry, and human physiology.

Let’s face it. At around 40 we all start to see signs of aging. It can’t be denied any longer at that point. You aren’t ready to be old. Some of us have been athletes all of our lives and are not ready to be fat and happy sitting in a sports bar watching ball on a wide screen. You want to keep going. So you seek a reason why you feel sub-par. Finally after seeing about a dozen doctors you run into one that tests some endocrine values and low and behold you find that your testosterone has tanked. You are told a normal 30 year old athletic male might test at 700 ng/dL and you are something like 220 ng/dL. Not only that but your IGF-1, a marker for GH release is in the bottom of normal range. So the doc asks have you used and anabolic steroids in the past? Have you had a blow to the head? Are you exposed to any toxins at your job etc etc. Oh shit!! Your manhood is diminishing. No wonder you look at young women like they are all your daughter and the wife just seems to nag at you without even speaking. You’re turning into an old man. You want to chase pkids out of your yard and keep their football. The doc says there is a number of treatments and he rattles off a bunch of antidepressants, a few vitamins, Cialis and then mumbles something like testosterone injections and crèmes and your ears perk up. Hell no you say to yourself. I’m not growing old just yet, at least not while there are androgens that come in little bottles.

The research towards the myostatin inhibitor ACE-031 was terminated - but it does work

The pharma companies Acceleron Pharma and Shire have put the myostatin inhibiter ACE-031 on ice. That have indicated. [Acceleronpharma.com May 2, 2013] And that's pretty weird. Them in a joint press release a few days ago

A few weeks earlier, Muscle & Nerve published a study showing that ACE-031 is a compound which a chemical bodybuilder would gladly add to his toolbox.

The injectable ACE-031  is a synthetic activin receptor type IIB. Muscle cells have that receptor too. It is intended for proteins as myostatin, GDF11 and activin A and B. If myostatin docks itself to the activin receptor type IIB, then the growth of muscle fibers reduces. Under the 'right' circumstances myostatin even breaks down muscle.

If you inject ACE-031, then that does not happen. The synthetical activin receptor type IIB captures the muscle inhibitory proteins away, and disable them.