Primobolan
(methenolone acetate) Primobolan is one of those anabolic steroids, which has a cult like the old original version of Masteron. Indeed, as can be seen from its anabolic: androgenic is lower in profile, it is rather weak steroid, but it is actually stronger (!) Masteron that in both cases. I do not know anyone who has the prospect of a connection to the same dose. We are probably justified in speculating that you will probably get similar results from one of them, given that you get a little less of the drug and more airtime when you choose the Primobolan injectable (which has a large enanthate ester attached) during Masteron (which has a very short propionate ester attached). In truth, I believe, in part, Primobolan, many users were disappointed that it is not enough to use it for long enough. Since its chemical structure and anabolic: androgenic rating, we can assume that it is at least as effective as equal Masteron mg mg base. However, because of its ester (in the version for injection), we must run for at least 12 weeks to see all the benefits thereof. If you think a miserable dose 400mg of this material for 12 weeks, probably cost about $ 500. It is easy to understand why many people try to use less ... and they were disappointed by their results. On the other hand, competition from many bodybuilders Primobolan indespensible consider their pre-competition Drud usual, and not consider a food without it. But ... I think the comparison with Masteron (another great precontest drugs) is the best we can do, given the expected results and outcomes. It remains one of the few people who use drostanolone enanthate (Masteron enanthate ester attached) as well as methenolone enanthate (Primobolan injectable). I can tell you that the results of these two compounds, when air power and mg are the same, in fact, very similar. Step Primobolan Allow us to clarify some of the different overall effects of Primobolan, before arriving at the distinction between oral and injectable versions ... A study on sheep in the administration of 100mg methenolone and electronically enabling lats (electronic stimulation was used, because they kept falling chin-up bar). In all cases, compared with LAT muscles of sheep that are not methenolone, the host team a lot more muscle mass and strength (1) (2). It also has a high affinity for binding to AR, in fact, better than the binding of testosterone (3). This ability to bind strongly with the AR Primobolan May be the reason why a good fat burner. " Strong AR-binding is positively correlated with lypolysis (fats) (8). In addition, as in May actually help reduce steroids breast tumors, but other products should be considered for use with Primobolan and in fact, in May this be a useful tool in its own right, similar to Masteron. In addition, like Masteron, Primobolan has no tendency to aromatization (conversion to estrogen). As she aromatization, many side effects commonly associated with estrogen do not worry. This means, retention, acne, and gyno will be no more or less. This lack of water combined with the slow and steady gains provided by Primo May help to explain why he has earned a reputation for creating quality muscle gains. This also helps explain why it is so expensive. Although the parties not estrogen anxiety, hair loss is a very real concern with Primobolan, like many DHT derived steroids. Many fans are still primobolan and finasteride Ketoconazole (shampoo) in cycles with Primobolan. Although no one has ever suggest using Primobolan agent, was studied as an agent to stop the loss and possibly a large number of reversing the adverse effects of anemia. It is a shocking failure in these two areas, according to some case studies I've read, (5) (6), and this should not come as a surprise for everyone. Anadrol reigns supreme in this area, and nobody in the sports community would never compare the two drugs. However, Michael Mooney, and many other doctors who work with AIDS patients have found sufficient evidence to say that the Primobolan is Immune Enhancer and as such is very useful for people living with AIDS (which is concerned about the FDA ... Primobolan are not yet approved for sale in the United States). AIDS patients, Bulking not need drugs, and immune system enhancer as Primo, adding a small improvement in the quality of the muscle is ideal for them. And since we do not even vaguely considering using Primobolan an agent, we clearly begin to consider for use in obtaining and maintaining lean tissue. It is an excellent choice for this purpose and many competitors have used successfully to retain muscle while on reducing calories. Why Primo is useful for this purpose is that one of its main functions is to help your body to maintain nitrogen (7) to strengthen significantly the course. Plus you retain nitrogen, the more muscle to build. In the case of Primo as a pre-contest drug, this retention of nitrogen will help you keep your muscles and make sure that your diet contributes to a loss of body fat primarily from the loss of muscle. Primobolan steroids unique in that it is one of the few that occurs at the hearing and the injection. I think, and Winstrol, but in fact, an ester of Primobolan oral (acetate) and injectable (enanthate) version. The oral version is one of the most interesting interpretations of compounds I looked. First, it is one of the few compounds for athletes and bodybuilders, which is both oral and non-17-alpha-alkylation. This change (and I'm sure you remember other things I have written), which is usually oral steroids to survive their first pass metabolism, but also makes Hepatoxic (liver? Toxic). Well ... Oral primo is not this feature, it is very gentle to the liver (in fact it is largely in the liver of all poisons), but also largely destroyed, and 17 and 1 beta estrification alkylation is the method used to make this material available orally. You'll need to take a lot of material that is effective ... 100mgs/day version of the oral cavity is a safe estimate of female success, you can go with a smaller, perhaps 25mgs/day. Although the acetate ester of the active life of 2-3 days, your liver will do some damage to the Primo oral daily dosage is needed. When men were given 30-45mg oral dose of Primo, they experienced a decline of 15-65% of the level of gonadotropin (9). Remember, I said it is a 100mg dose to achieve good ... Well, you can also reduce the level of gonadotropin significantly. Personally, I never understood why people recommend that the oral or injectable Primobolan can overcome the complex for this reason ... May be too low-DO-a dose of 10mg may be used as a link. And forget using injectable Primo on deck and Hey ... Talking about injectable Primo ... I used this material in 200mgs/week and was not very impressed by him. In general, I think, Primo injection should be used at a dose of at least 350mgs/week (100mgs/Every another day), and preferably at a dose of 400-600mgs/week. For me, it works with testosterone propionate, but for practical reasons, I think most people is the testosterone enanthate, in order to maintain the same dosing times (shooting twice a week, in most cases). Buy Primobolan Unfortunately, the truth about injectable Primo, it is very costly to obtain chemicals and the price is factored into the costs for the average consumer. Ten dollars per bulb 1ml/100mg not heard, and I saw him do much more. This, of course, absurd. As if this were not enough, it is also the most often counterfeited steroids on the black market. I recommend to buy Primobolan (oral or injectable) renowned underground lab, rather than playing the game "spot fake steroids" in Mexico and Europe. The underground version costs $ 5.7 per 100mg of methenolone and I would not consider to pay more for it, but I have seen British Dragon version of the product, the price to $ 20/ml. Primobolan profile (Methenolone) (Oral acetate Ester + version) (Version enanthate injection + Ester) [17beta-hydroxy-1-methyl-5alpha-androst-1-ene-3-one] Molecular weight of base: 302.4558 The molecular weight acetate ester: 60.0524 Enanthate ester Molecular Weight: 130.1864 Formula: C20H30O2 Melting point: Manufacturer: Schering Effective dose (oral): (Men) 50-100mgs/day (Women) 10-25mgs/day Effective dose (injectable) (Men) 350-600mgs/week (Women) 100mgs/week Active Life: 10-14 days (for injection), 4-6h (oral) Detection time: 4-5 weeks Anabolic / Androgenic Ratio (Range): 88:44-57 References: Anabolic steroids (metenolone) improvement of muscle activity and hemodynamic characteristics cardiomyoplasty. Ann Thorac Surg. April 1995, 59 (4) :961-9, discussion 969-70. Impact on anabolic steroids (metenolone) on the contractile performance of the chronically stimulated latissimus muscle of sheep. Eur J Cardiothorac Surg. 1994, 8 (4) :214-9. Relative binding affinity of anabolic-androgenic steroids: comparison of binding to androgen receptors in skeletal muscle and the gland and the hormone-binding globulin sex. Endocrinology. June 1984, 114 (6) :2100-6. [Anabolic therapy of metastatic breast cancer] Med Klin. 20 November 1981, 76 (24) :689-91. German. Partial remission and severe adverse reactions caused by metenolone acetate in a male patient with aplastic anemia. Eur J Haematol. 55 July 1995 (1) :57-8. Death of a patient with severe aplastic anemia after treatment with acetate metenolone. Ann Hematol. July 1993, 67 (1) :41-3. Metabolic effects of anabolic steroids. Wien Med Wochenschr. 1993, 143 (14-15) :368-75. Biochim Biophys Acta. 11 May 1995; 1244 (1) :117-20. Comparative studies on the impact of MetenoloneAcetate mesterolone and pituitary and male gonads. Arzneimittelforshung. 1970 20 (4) 545-7
вторник, 21 июля 2009 г.
Pituitary Growth Hormone (pGH)
Pituitary growth hormone
(PGH) Growth hormone is a protein hormone that is produced and provided cells in the pituitary somatotrophs. It monitors and / or the effects of many physiological processes, including muscle growth and metabolism of lipids. When it is generated within the body, it is called endogenous - and when it is performed by an external source, it is called exogenous. Growth hormone, like many other hormones have direct effects (acting directly on tissues and cells) and indirect effects (stimulating the release or synthesis of hormones, eg IGF-1, which in its turn, the effect of tissue and cells on its own). Muscle cells have receptors for growth hormone and IGF-1 receptors. When growth hormone and IGF-1 is introduced into muscle cells, the cells are created and existing cells increased. These responses are known as hyperplasia and hypertrophy, and processes that contribute to the growth of other muscles. Growth hormone also has the ability to directly influence the loss of fat, and fat cells have receptors, growth hormone. If growth hormone in fat cells, the result is that fat cells and easier to use for energy. This process is known as lipolysis, commonly known as "burn fat", which is simply the conversion of fat into energy. However, despite the muscle cells have a growth hormone, and IGF 1 ¬ receptor for growth hormone have direct and indirect effects, fat cells do not have IGF-1 receptors. IGF-1, which stimulates the production of growth hormone, work independently to burn fat in the body by activating the protein, fat and carbohydrate metabolism. Thus, growth hormone has direct and indirect effects on the promotion of muscle growth and fat loss. Finally, based on anecdotal reports from experienced people with growth hormone, the results are evident 6-8 weeks. At week 6-point, athletes tend to report that the results are beginning to appear, but 12 weeks (and beyond), increasing muscle mass and fat loss are nothing less than fantastic. That is why athletes often remain in the chamber for a minimum period of two months, but usually closer to three or four months at a time.
(PGH) Growth hormone is a protein hormone that is produced and provided cells in the pituitary somatotrophs. It monitors and / or the effects of many physiological processes, including muscle growth and metabolism of lipids. When it is generated within the body, it is called endogenous - and when it is performed by an external source, it is called exogenous. Growth hormone, like many other hormones have direct effects (acting directly on tissues and cells) and indirect effects (stimulating the release or synthesis of hormones, eg IGF-1, which in its turn, the effect of tissue and cells on its own). Muscle cells have receptors for growth hormone and IGF-1 receptors. When growth hormone and IGF-1 is introduced into muscle cells, the cells are created and existing cells increased. These responses are known as hyperplasia and hypertrophy, and processes that contribute to the growth of other muscles. Growth hormone also has the ability to directly influence the loss of fat, and fat cells have receptors, growth hormone. If growth hormone in fat cells, the result is that fat cells and easier to use for energy. This process is known as lipolysis, commonly known as "burn fat", which is simply the conversion of fat into energy. However, despite the muscle cells have a growth hormone, and IGF 1 ¬ receptor for growth hormone have direct and indirect effects, fat cells do not have IGF-1 receptors. IGF-1, which stimulates the production of growth hormone, work independently to burn fat in the body by activating the protein, fat and carbohydrate metabolism. Thus, growth hormone has direct and indirect effects on the promotion of muscle growth and fat loss. Finally, based on anecdotal reports from experienced people with growth hormone, the results are evident 6-8 weeks. At week 6-point, athletes tend to report that the results are beginning to appear, but 12 weeks (and beyond), increasing muscle mass and fat loss are nothing less than fantastic. That is why athletes often remain in the chamber for a minimum period of two months, but usually closer to three or four months at a time.
Parabolan (trenbolone cyclohexylmethylcarbonate)
Parabolan
Parabolan is one of these medicines, which are of short duration (Negm finally dragged on the market) and made a huge impact very quickly. Dan Duchaine was the first person to write about it in his underground complex Steroid Handbook Update Newsletter. In his writings, he suggested that you do not want to go over 2 amps per week of the original product Negm (amps each is 76mg, and if you want to know why this is so, because each gives the Ampère user specifically 50mg trenbolone after your body by esterases separated from HexaHydroBencyl Carbonate ester). Unfortunately, not many people really have a chance to experiment with the original Parabolan, as it was withdrawn from the market very quickly Negm (abolished in 1997). This creates a very strange situation where the product is used with success, several people in a very short time, then, in principle, inaccessible after. It is essentially created a cult for drugs. Past decade, and counterfeits stormed the market until Duchaine (again) wrote an article on the extraction of trenbolone Finaplex pellet, then sterilize in order to create your own trenbolone acetate, even if it ' was not Parabolan, it soon reduced the popularity of counterfeit Parabolan. Tren was Tren, in most eyes, regardless of the ether. "Fina" kit "(complete set, which allows the owner of the station) and then flooded the market, using a loophole in which the pellets and kit were purchased legally, but it is clear that the manufacture and use of steroid injections in the kitchen, is illegal. Blinks a few years, trenbolone acetate is available, many laboratories, and trenbolone enanthate became available, and now, even Parabolan (which is the basis for Trenbolone + A HexaHydroBencyl Carbonate Ester) is readily available in most major laboratories. Steroid.com A visit to any person or a larger forum to testify that Parabolan's cult has not yet been reduced. Let's see why. Parabolan neither affected by aromatase or 5alpha-reductase. This means that it is neither weak nor very sensitive to androgen target tissues, and this function is generally shared by DHT (DyhydroTestosterone) received steroids; Since Parabolan, of course, trenbolone, it is not DHT derived but rather, it stems from the 19-Nor-testosterone .. Parabolan no estrogenic activity (May actually reduce the level of estradiol in the body), is a very strong anabolic and androgenic compounds (5x stronger than testosterone in both categories!), And it binds to receptors of androgens. In fact, binding "good" to the androgen receptor is very low. There is no injectable AAS in our arsenal that binds to the androgen receptor (AR) and trenbolone ago. This is probably one of the main reasons that Parabolan so saught after for use as an agent precontest. Androgen receptors in fat cells and muscle cells (8), and we all know that they act on the AR in muscle cells to stimulate growth, but they androgens act directly on the AR in fat cells to burn fat influences. (9) (6) Strengthening the androgen binds to the RA, above lipolytic (fat) on body fat (FAT), textiles (9) (5). As if this were not enough good news, steroids even increase the number of RA in the muscle and fat (9) (10), which led me to speculate that this fat loss effect would be reinforced by the simultaneous use of other compounds such as testosterone injections. Another mechanism that Parabolan causes muscle accumulation and fat loss is its capacity as agent of nutrient partitioning. (7) In principle, this means that while using Tren, more food you eat and the muscles become smaller (if any) will be fat. Indeed, as you can see, most of Parabolan in a cult reputation is well deserved ... And as if this were not enough, Parabolan significantly increased the level of IGF-1 in muscle tissue (2), which in itself is an anabolic hormone. And it is interesting to note that not only increase the level of IGF-1 in muscle more than twice (2), it also causes muscle satellite cells (the cell repair damaged muscles), which would be more sensitive with IGF-1 and other growth factors (3). This leads me to assume that Parabolan (or any other version of Tren) would be synergistic within a cycle containing any form of IGF-1 injection. Parabolan also happens to bind strongly to glucocorticoid receptors, as well as this, in turn, provides an anti-catabolic effect ... What help in May partly explain why low (ish) doses, it seems to work fine, and the reasons for loss of grease AIDS. You see, glucocorticoid hormones send a message to muscle cells to release stored protein (this is called catabolism), which is exactly the opposite, that we want. This medication especially batteries and all, especially testosterone (in fact, if you want to avoid sexual dysfunction, stacking of testing required). I also found that what is great to stack containing the equation, but unfortunately the insomnia the Parabolan gives me added appetite equalizer me midnight snacking almost inevitable. Parabolan is most often used in the cutting of the batteries when the "quality muscles" favored strengthening the size and water. In fact, I think Parabolan (or friction) is very "strong" anabolic but it has been used successfully by many as Bulking and cutting cycles. It's not all good news, but ... Parabolan Side Effects Some users report sexual dysfunction Torque (Tren-Dick) and symptoms of gyno (probably progesterone related, effective trenbolone on progesterone receptor but not estrogen receptor). As you know, trenbolone, unfortunately, a progestin: it binds to the receptor of progesterone, female sex hormone (about 60% of the actual progesterone) (4). In the hyper-sensitive steroid.com members, this can lead to increase growth and breast in combination with estrogen or aromatization product, but probably not (14), worse yet, the active metabolite Trenbolone (17beta-trenbolone ) has a binding affinity for the receptors of progesterone, which is actually greater than progesterone itself (5). There was no panic, however, the aromatase inhibitor Lertrozole May also reduce the level of progesterone, and to fight against all parties progestenic (15) (16). I would strongly consider its inclusion in .25-.5mgs/day in a cycle containing Parabolan or 19-nor complex. Paradoxically, despite the section is an excellent cutting drug, it will be below the level of your thyroid gland (11). At the same time, using the body-negative feedback cycle, and increases in prolactin. Ergo, I recommend taking T3 (25mcgs/day) with your Tren to avoid suffering from increased levels of prolactin and a host of undesirable side effects that result in May. For these reasons, many people avoid stacking Tren with a bridge (nandrolone decanoate), which is also a progestin (4). Mental changes in the well-known side effect of any type of trenbolone use (12), and the issue is no exception to this rule. Androgens increase chemicals in the brain that promote aggressive behavior (13), which May be useful for some athletes wanting to improve the speed and power, but perhaps at the expense of those trying to work as an employee social. Fortunately, I have not known as an ambassador of good will, in general, this side effect is largely unnoticed by me. For me, the worst effects of any kind Trenbolone is "Tren cough" which I get over the first 2 weeks of my cycle, and includes the connection. Tren enanthate not have that effect on me, but sometimes Parabolan; acetate Tren gives me a negative Tren-Cough in the first week, or that I am at it. In addition, any Tren gives me a little sleep, which is common to many users. The most notable side effect of Parabolan for me is that it increases my sweating dramatically, even giving me vicious "night sweats" perfectly with my insomnia. Mounted at May I also penetrate pearls, then, when I have about this product. In addition, it should be noted that many people experience reduced cardiovascular using the clause (12), and I fall into this category. Nevertheless, a tremendous impact on my strength and appearance mean that this will be my rounds of the season and winter (when sweating is not so much on the problem). Parabolan Profile (Trenbolone Base + HexaHydroBencyl Carbonate Ester) [17beta-hydroxyestr-4 ,9,11-trien-3-one] Formula: C20 H24 O3 Molecular Weight (base): 270.3706 Molecular Weight (ester): 130.1864 Formula (base): C18 H22 O2 Melting Point (base): 183-186C Manufacturer: (originally) Negm, Various Underground Labs Effective Dose (men): 300-500mgs/week Effective Dose (Women): Not recommended Active Life: 5-7 days Detection time: 4-5 weeks Anabolic / Androgenic ratio: 500/500 References: Br J Nutr. 1978 Nov; 40 (3) :563-72. J Cell Physiol. 2004 Nov; 201 (2) :181-9. Endocrinology. May 1989; 124 (5) :2110-7. Cancer Res 1978 Nov 38 (11 Pt 2) :4186-98 APMIS. December 2000, 108 (12) :838-46. (Xu X et al. Effect of androgens on the regulation of lipolysis in fat cells. Endocrinology 1990 Feb; 126 (2): 1229). J Anim Phys.-Math. 1992 Nov; 70 (11) :3381-90. Am J Physiol. June 1998, 274 (6 Pt 1): C1645-52. Biochim Biophys Acta. 11 May 1995; 1244 (1) :117-20. J Appl. Physiol.94 1153-61 2003 Res Vet Science 1981 Jan, 30 (1) :7-13 Steroid.com forums. Med Science Sports Exerc. January 2003, 35 (1) :32-8 Progesterone is not essential to the differentiation potential of the epithelium of mammary glands in male mice. Freeman, Topper. Endocrinology. July 1978; 103 (1) :186-92 Eur J Obstet Gynecol Reprod Biol. 2002 Nov 15; 105 (2) :161-5. J Clin Endocrinol Metab. 1995 Sep; 80 (9) :2658-60.
Parabolan is one of these medicines, which are of short duration (Negm finally dragged on the market) and made a huge impact very quickly. Dan Duchaine was the first person to write about it in his underground complex Steroid Handbook Update Newsletter. In his writings, he suggested that you do not want to go over 2 amps per week of the original product Negm (amps each is 76mg, and if you want to know why this is so, because each gives the Ampère user specifically 50mg trenbolone after your body by esterases separated from HexaHydroBencyl Carbonate ester). Unfortunately, not many people really have a chance to experiment with the original Parabolan, as it was withdrawn from the market very quickly Negm (abolished in 1997). This creates a very strange situation where the product is used with success, several people in a very short time, then, in principle, inaccessible after. It is essentially created a cult for drugs. Past decade, and counterfeits stormed the market until Duchaine (again) wrote an article on the extraction of trenbolone Finaplex pellet, then sterilize in order to create your own trenbolone acetate, even if it ' was not Parabolan, it soon reduced the popularity of counterfeit Parabolan. Tren was Tren, in most eyes, regardless of the ether. "Fina" kit "(complete set, which allows the owner of the station) and then flooded the market, using a loophole in which the pellets and kit were purchased legally, but it is clear that the manufacture and use of steroid injections in the kitchen, is illegal. Blinks a few years, trenbolone acetate is available, many laboratories, and trenbolone enanthate became available, and now, even Parabolan (which is the basis for Trenbolone + A HexaHydroBencyl Carbonate Ester) is readily available in most major laboratories. Steroid.com A visit to any person or a larger forum to testify that Parabolan's cult has not yet been reduced. Let's see why. Parabolan neither affected by aromatase or 5alpha-reductase. This means that it is neither weak nor very sensitive to androgen target tissues, and this function is generally shared by DHT (DyhydroTestosterone) received steroids; Since Parabolan, of course, trenbolone, it is not DHT derived but rather, it stems from the 19-Nor-testosterone .. Parabolan no estrogenic activity (May actually reduce the level of estradiol in the body), is a very strong anabolic and androgenic compounds (5x stronger than testosterone in both categories!), And it binds to receptors of androgens. In fact, binding "good" to the androgen receptor is very low. There is no injectable AAS in our arsenal that binds to the androgen receptor (AR) and trenbolone ago. This is probably one of the main reasons that Parabolan so saught after for use as an agent precontest. Androgen receptors in fat cells and muscle cells (8), and we all know that they act on the AR in muscle cells to stimulate growth, but they androgens act directly on the AR in fat cells to burn fat influences. (9) (6) Strengthening the androgen binds to the RA, above lipolytic (fat) on body fat (FAT), textiles (9) (5). As if this were not enough good news, steroids even increase the number of RA in the muscle and fat (9) (10), which led me to speculate that this fat loss effect would be reinforced by the simultaneous use of other compounds such as testosterone injections. Another mechanism that Parabolan causes muscle accumulation and fat loss is its capacity as agent of nutrient partitioning. (7) In principle, this means that while using Tren, more food you eat and the muscles become smaller (if any) will be fat. Indeed, as you can see, most of Parabolan in a cult reputation is well deserved ... And as if this were not enough, Parabolan significantly increased the level of IGF-1 in muscle tissue (2), which in itself is an anabolic hormone. And it is interesting to note that not only increase the level of IGF-1 in muscle more than twice (2), it also causes muscle satellite cells (the cell repair damaged muscles), which would be more sensitive with IGF-1 and other growth factors (3). This leads me to assume that Parabolan (or any other version of Tren) would be synergistic within a cycle containing any form of IGF-1 injection. Parabolan also happens to bind strongly to glucocorticoid receptors, as well as this, in turn, provides an anti-catabolic effect ... What help in May partly explain why low (ish) doses, it seems to work fine, and the reasons for loss of grease AIDS. You see, glucocorticoid hormones send a message to muscle cells to release stored protein (this is called catabolism), which is exactly the opposite, that we want. This medication especially batteries and all, especially testosterone (in fact, if you want to avoid sexual dysfunction, stacking of testing required). I also found that what is great to stack containing the equation, but unfortunately the insomnia the Parabolan gives me added appetite equalizer me midnight snacking almost inevitable. Parabolan is most often used in the cutting of the batteries when the "quality muscles" favored strengthening the size and water. In fact, I think Parabolan (or friction) is very "strong" anabolic but it has been used successfully by many as Bulking and cutting cycles. It's not all good news, but ... Parabolan Side Effects Some users report sexual dysfunction Torque (Tren-Dick) and symptoms of gyno (probably progesterone related, effective trenbolone on progesterone receptor but not estrogen receptor). As you know, trenbolone, unfortunately, a progestin: it binds to the receptor of progesterone, female sex hormone (about 60% of the actual progesterone) (4). In the hyper-sensitive steroid.com members, this can lead to increase growth and breast in combination with estrogen or aromatization product, but probably not (14), worse yet, the active metabolite Trenbolone (17beta-trenbolone ) has a binding affinity for the receptors of progesterone, which is actually greater than progesterone itself (5). There was no panic, however, the aromatase inhibitor Lertrozole May also reduce the level of progesterone, and to fight against all parties progestenic (15) (16). I would strongly consider its inclusion in .25-.5mgs/day in a cycle containing Parabolan or 19-nor complex. Paradoxically, despite the section is an excellent cutting drug, it will be below the level of your thyroid gland (11). At the same time, using the body-negative feedback cycle, and increases in prolactin. Ergo, I recommend taking T3 (25mcgs/day) with your Tren to avoid suffering from increased levels of prolactin and a host of undesirable side effects that result in May. For these reasons, many people avoid stacking Tren with a bridge (nandrolone decanoate), which is also a progestin (4). Mental changes in the well-known side effect of any type of trenbolone use (12), and the issue is no exception to this rule. Androgens increase chemicals in the brain that promote aggressive behavior (13), which May be useful for some athletes wanting to improve the speed and power, but perhaps at the expense of those trying to work as an employee social. Fortunately, I have not known as an ambassador of good will, in general, this side effect is largely unnoticed by me. For me, the worst effects of any kind Trenbolone is "Tren cough" which I get over the first 2 weeks of my cycle, and includes the connection. Tren enanthate not have that effect on me, but sometimes Parabolan; acetate Tren gives me a negative Tren-Cough in the first week, or that I am at it. In addition, any Tren gives me a little sleep, which is common to many users. The most notable side effect of Parabolan for me is that it increases my sweating dramatically, even giving me vicious "night sweats" perfectly with my insomnia. Mounted at May I also penetrate pearls, then, when I have about this product. In addition, it should be noted that many people experience reduced cardiovascular using the clause (12), and I fall into this category. Nevertheless, a tremendous impact on my strength and appearance mean that this will be my rounds of the season and winter (when sweating is not so much on the problem). Parabolan Profile (Trenbolone Base + HexaHydroBencyl Carbonate Ester) [17beta-hydroxyestr-4 ,9,11-trien-3-one] Formula: C20 H24 O3 Molecular Weight (base): 270.3706 Molecular Weight (ester): 130.1864 Formula (base): C18 H22 O2 Melting Point (base): 183-186C Manufacturer: (originally) Negm, Various Underground Labs Effective Dose (men): 300-500mgs/week Effective Dose (Women): Not recommended Active Life: 5-7 days Detection time: 4-5 weeks Anabolic / Androgenic ratio: 500/500 References: Br J Nutr. 1978 Nov; 40 (3) :563-72. J Cell Physiol. 2004 Nov; 201 (2) :181-9. Endocrinology. May 1989; 124 (5) :2110-7. Cancer Res 1978 Nov 38 (11 Pt 2) :4186-98 APMIS. December 2000, 108 (12) :838-46. (Xu X et al. Effect of androgens on the regulation of lipolysis in fat cells. Endocrinology 1990 Feb; 126 (2): 1229). J Anim Phys.-Math. 1992 Nov; 70 (11) :3381-90. Am J Physiol. June 1998, 274 (6 Pt 1): C1645-52. Biochim Biophys Acta. 11 May 1995; 1244 (1) :117-20. J Appl. Physiol.94 1153-61 2003 Res Vet Science 1981 Jan, 30 (1) :7-13 Steroid.com forums. Med Science Sports Exerc. January 2003, 35 (1) :32-8 Progesterone is not essential to the differentiation potential of the epithelium of mammary glands in male mice. Freeman, Topper. Endocrinology. July 1978; 103 (1) :186-92 Eur J Obstet Gynecol Reprod Biol. 2002 Nov 15; 105 (2) :161-5. J Clin Endocrinol Metab. 1995 Sep; 80 (9) :2658-60.
Oxantrione (Var 10)
Oxantrione
(Var 10) Oxantrione known as one of the safest products on the market. It is not as effective as most bodybuilders want to make it less popular. For those who want a clean environment, security products with strong results and a very low chance of side effects, this product is for you! It is widely used in large loops, as an effect stronger than the anabolic androgen. Most people are satisfied with the results they get from this product. It is an ideal entry product, as well. Dosage: Hit hard on 10 mg 3 times daily from the start. Most users will find a good dose of 8-12 weeks of the cycle. Side effects: Oxantrione has a very low level of side effects. Only a low testosterone related parties has ever said about this product. Identity Theft: Oxantrione to buy very safe compared to most drugs and supplements today. This is not high on the list fall between counterfeiters because it is in lower demand compared to other products. Counterfeiters tend to focus on products with big names that are largely demand, which makes it very safe Oxantrione buying! Var, research anabolic is the most popular product Oxantrione.
(Var 10) Oxantrione known as one of the safest products on the market. It is not as effective as most bodybuilders want to make it less popular. For those who want a clean environment, security products with strong results and a very low chance of side effects, this product is for you! It is widely used in large loops, as an effect stronger than the anabolic androgen. Most people are satisfied with the results they get from this product. It is an ideal entry product, as well. Dosage: Hit hard on 10 mg 3 times daily from the start. Most users will find a good dose of 8-12 weeks of the cycle. Side effects: Oxantrione has a very low level of side effects. Only a low testosterone related parties has ever said about this product. Identity Theft: Oxantrione to buy very safe compared to most drugs and supplements today. This is not high on the list fall between counterfeiters because it is in lower demand compared to other products. Counterfeiters tend to focus on products with big names that are largely demand, which makes it very safe Oxantrione buying! Var, research anabolic is the most popular product Oxantrione.
Oral Turinabol
Oral-Turinabol
Oral Turinabol was first developed by scientists in East Germany for the Olympic athletes and national level for use. This, as well as possible to eliminate from the market caused OT to become very "sexy" for the athletes of drugs to try to get it. In East Germany, the drug studied in detail for many years, and some success in this country has now disappeared because of this drug, which made its first performance of athletes in the east of the Germany as little blue "Vitamins" their coaches gave them. This drug has been stopped at all the major pharmaceutical companies, but only through some underground laboratory. Although some sub-Labs have access to this issue and it appears on the lists of prices, it is still quite rare. I think this is the first time during the last decade and a half to a cat in Thailand. It is my hypothesis that the threshold of becoming very popular to the point where every Underground Lab will have its own version, or it will disappear, and then select only a few, if any suppliers. The easiest way to explain is that this drug is a derivative of Dianabol. Although it is a derivative of our old friend Diana, it is always ... Remember that balance is estrified Dianabol, and really has nothing to do with it, in terms of real-world implications. Take the OT with respect to the D-ball now, though. The first similarity between them is that they were both 17-alpha-alkylated (a carbon atom has been included in the 17th position) to survive the first pass through the liver. This, of course, increases hepatoxicity (liver toxicity). OT has a much lower level of activity compared to Dianabol androgens, but a better balance and the ratio of anabolic androgenic effects. It has a 0 rating (according to the Vida reference) for androgenic properties, steroids, and 53 for the properties on the basis of 100 points each for testosterone. This contributes to a more "rigid" Look, that competition bodybuilders often call "quality" muscle. You can not get the same "inflated" Look, how would you do with the D-bol, and many people in this way, compared to the results they have received from OT to Anavar. In reality, however, this material is simply Dianabol with 4-chloro changes, the same changes in clostebol. In this regard, the 4-chloro substitution in the A-ring Steran its Nucleus, the drug can not be aromatized (3). This, as you know, it is very useful and is one of the reasons Oral Turinabol been described as "gentle d-bol." You probably will not receive any estrogenic side effects like water retention, acne, gyno, etc, at a dose of the drug. Several studies I read examining male athletes over six weeks were given 10 mg OT / day did not show any signs of health danger. It is recommended that men should take between 20-40 mg per day, 5 mg and women every day, and I think in general it is not very strong (compared to many other oral) and not fall below 40 mg per Mark, if I had to use it personally. It May be used in low (ER) doses, if used only for its ability to reduce SHBG binding in (1) other steroids. In this regard, it May interact with other medicines, because it has the ability to reduce SHBG and thus free up more testosterone for use in your body. The only negative point that I heard of this drug is at high dose (10 + mg) virilization seen in women (14), and there was at least one case of testicular tumor, and one case of a guy who have suffered adverse effects from 5 years of use at high dose of P (2) (4). It should be noted that in the former East Germany has made a lot of experimentation with drugs in high doses, however, and found that it is a very suitable compound for their athletes. Many women suffered virilization at higher doses, however. During the 68-72 Olympic cycles, the East German Sports OT program made its biggest impact. At this time, East Germany took 10g/year weightlifters in overtime, as well as their main men took Sprinter 730mgs/year of OT (14). I think this tells me that for weight gains, and huge gains in the gym, you will need to break the bank of doses of this product. On the positive side, if you are a candidate for athletes faster, a little OT, it will be very quickly and with minimal (if any) side effects). I think the inability to cause negative side effects, and its ability to produce a favorable increase in lean body mass and thus a favorable increase in strength and speed and strength of an athlete: body ratio is the fact that transformed East Germany on the coaches and scientists. It should be noted that when this story is essentially undetectable, and this, of course, look for signs in the East Germans seeking to circumvent the testing procedures of drugs for the IOC. Now, of course, OT detected and after it is administered with a man, three major metabolites are formed: 6-beta-hydroxy-turinabol, 6 beta, 12-dihydroxy-turinabol and 6 beta, 16-dihydroxy - turinabol (5 ) (8) (9). All these metabolites are detectable drug screening. In many small amounts of at least three others are the excretion of metabolites, one of which is defined as May 17 epi-turinabol (5), which can be easily detected by testing modern ... No measurable OT is detected in any of urine proceedings against doping in sport, but the presence of metabolites sufficient for a positive result and a failed test. Keep all this in mind, it is important to note that the rate of metabolism and excretion of urine or oral Turinabol fast enough (5), although it is technically eliminated biphastically (in two parts) on the body, with the 16hr terminal half life (1). I think the sport of doping Poopers part (in the NCAA and IOC) OT is known to increase the time needed for your blood clot, as it is spontaneous fibrinolytic properties. "Fibrinolytic effects" means that the destruction of fibrin (insoluble fibrous protein produced in the liver of soluble protein) that occurs in your body. Fibrinogen is important in the process of blood clotting, as well as soluble proteins in the blood, which is converted into insoluble fibrin by the action of the enzyme thrombin in response to tissue damage. (6) (7) So you bleed longer than usual, when this material, combined with the fact that steroids raise your hematocrit and spend all morning trying to stop the bleeding, if you 're shaving. Well, this is probably an exaggeration, but not much. Oral Turinabol Olympic cycle I said that this story is a lean tissue builder, and good for cutting. But it is mainly of interest to bodybuilders. Now, with regard to athletics, the results can we expect? Well, I searched the literature in former East Germany, and found that they indicated that the number of world-class athletes are very clear improvement on the situation of at least 4 years of training period Olympic Men's Shot-putters were adding 2.5-4M shooting their free throws, 10-12M on their disk, and 6-10M with their Hammer throws. Female athletes gained even more. Let's look at the chart of improvements made by an individual, the strength of female athletes (* it has the world record shot put at the time of his departure OT administration), during the period of 18 to 13 July 1968 October, 1972. At that time he was in occupational therapy, has improved his throwing 18M 20m (yes, that is 2m + improvement, the world record of the Olympic Games while cycle). It takes about 5-15mgs/day of OT in the beginning, but 35mgs/day worked before she made her Olympic cycle. It throws while "OFF" OT even improved a little, leading to speculation that there are many successes to stand with the OT. Anyway, here in the admission patterns of OT, as well as improvements to this for 4 years, 4 years of her Olympic training regime: Effects on androgenic-anabolic steroid, Oral-Turinabol in the shot-put performance (in meters, the Y axis) of the female athlete (code identification 1 / 68 to 1 / 69 b, 1 / 72 c) directly photographed secret scientific report of Bauersfeld et al. (13) as one of the many documented examples, chosen because it is its historical significance as the first documented case of androgenic doping of a woman (for details see ref. (11)). (a) 1968. Rectangle from July 28 to 13 in October, said the period of drug administration, and the above figures show the daily number of tablets per week (in this case, 14 or 10 mg / day). The curve represents the results of competitions, an increase of the strength and performance of a fully trained woman. During the first use of drugs in 1968, athletes were well prepared for almost 14 years. Under the influence of drugs, however, she received an unprecedented number of improving muscle strength and records dramatically within a few weeks. (b) 1969. In the steroid was given in three cycles, and in various dosages, from 7 to 21 tablets per week (ie 5? 15 mg per day). Without the drugs, it can reach 18 meters, and when shooting drugs, she improved her world record once again at 20.10 h (C) 1972. It took even more of the hormone androgen, with daily doses of up to 7 pills a day (35 mg) in four cycles, for a total androgenic load of 1450 mg for one year. This led to the beginning of his speech within the winter season (left curve) and summer (right curve) and another staff (20.22 m). Pay attention to the significantly lower during the drug or after a short period of androgenization. In addition, after 4 years of systematic androgenization, its basic strength, even when not taking the drug also increased by ~ 1 m, indicative of a residual force. (14) Does all this work for those? Well, as I said earlier, almost everyone who took part in the Olympic program is German for steroids in one way or another, but the Old Testament was away, and most popular. They have access to some very strange, and too much testosterone intranasal, etc. And So ... Back to the Old Testament ... it differs from my testimony in this complex was that women are much more positive effect on OT than men (which applies to all steroids, though). In addition, women have more side effects, and generally have more serious side effects and unbearable than their male colleagues. Unfortunately, they also (sometimes), generally use higher doses than men, often up to 2x higher. Lets take a look at their type of doses per year: Some documents doses of anabolic-androgenic steroids (Oral-Turinabol) 1 adopted by the GDR medalists for women (athletics), the Olympic Games, World Championships and European Championships.2 (OT annual dose of MSG and events) 3680-Shot put 3190 Discus 2900-Shot put 2615-Shot put 2590-Shot put 1670 Sprint 1560 constraints 1480 constraints 1474 Sprint 1460 Sprint 1450-Shot put 1405 Sprint Heptathlon 1380 1375 Sprint Heptathlon 1340 1255 Discus Heptathlon 1230 1230 constraints 1185 javelin 1. Other esters of testosterone injections are not considered. 2. Data from ref. (14), which gives names and details. At least 12 of the drug-receiving competitors listed in the table of world records to save. In accordance with Journal policy regarding confidentiality of patients and subjects, the names of the elements were deleted. Shocked? Do not. It was during the Cold War and victory in the Olympic Games was seen as a victory for a certain lifestyle and certain ideologies, defeat is unthinkable and unacceptable. Does the recent resurgence of Oral-Turinabol on the black market will change in athletics and bodybuilding dramatically? № .. I doubt it ... combination of price ($ 1/10mgs average), and availability can lead to things that are undervalued tool at our disposal. However, it is a viable tool in weight of the meat-cutting cycle, cycle, or any athlete under drugs. In the finals, I'll give you an example (direct from the East German State Doping Program reports) on how they are used in the Old Testament, as well as several other drugs (eg, Prop. test by example): (Anabolic and special preparation for the commencement of the competition this year in direct training in the Olympic cycle 1980-84, for example, selected long jumpers (W) and high jumper (H) in conjunction with the results of competitions during this period) Example (from hundreds of evaluations) showing typical patterns oral administration of synthetic anabolic-androgenic steroids (Oral-Turinabol application period indicated by rectangles) and injections of testosterone ester [arrows, 10 mg propionate testosterone (TP), triangles, 25 mg of TP; circles, 100 mg of testosterone enanthate plus 1500 IU of hCG], here is a height (H) and long (W, Weitsprung) riders in the last 10 weeks before a major international competition in 1981? 1984 [immediate preparation period (UWV), in the week indicated on the X axis, a competition of the previous series UWV; competition results (in meters) above the drug application symbols]. (14) Oral Turinabol profile (4-chlorodehydromethyltestosterone) [4-chloro-17b-hydroxy-methyl-17A-androst-1 ,4-dien-3-one] Molecular Weight: 334.8854 Formula: C20H27O2Cl Manufacturer: Underground Labs only Effective Dose (men): 10-40mgs/day Effective Dose (Women): 5-15mgs/day Working life: 16 hours Detection time: 6 weeks Anabolic / Androgenic ratio:> 100:> 0 References: [The pharmacokinetics of Oral-Turinabol of Man] Pharmazie. 1991 Sep; 46 (9) :650-4. German. Department of Urology, Universitaetsklinikum "Carl Gustav Carus", Technical University of Dresden, Dresden, Germany 1-Effect of double bond and 11-beta-hydroxy group Stereospecific microbial reduction of 4-ene-3-oxo-steroids. J Steroid Biochem. October 1986, 25 (4) :561-6. Intratesticular leiomyosarcoma in a young man after high dose doping with Oral-Turinabol: case report. Cancer. 1999 Oct 15; 86 (8) :1571-5. GC capillary column and GC / MS for the determination of synthetic anabolic steroids. II. 4-chloro-methandienone (oral turinabol) and its metabolites. J Chromatogr Phys.-Math. 1983 Sep; 21 (9) :405-10. [Activation of the fibrinolytic system dehydrochlormethyltestosterone] Folia Haematol Int Mag Klin Morphol Blutforsch. 1984, 111 (4) :556-62. German. [Change hypofibrinolytic States dehydrochlormethyltestosterone] Folia Haematol Int Mag Klin Morphol Blutforsch. 1984, 111 (4) :563-6. German. [Application of microbial enzymes in studies of steroid substances (author's transl)] Acta Microbiol Acad Sciences Hung. 1975, 22 (4) :397-402. Review. German. [Application of microbial enzymes in studies of steroid substances (author's transl)] Acta Microbiol Acad Sciences Hung. 1975, 22 (4) :397-402. Review. German. [On the pharmacology "ORAL TURINABOL.] Dtsch Gesundheitsw. 1965 Apr 15; 20:690-1. German. No abstract available. Berendonk B. doping. Von der Forschung zum betrug. Reinbek bei Hamburg: Rowohlt Taschenbuchverlag. 1992:448 p. [4-CHLORO-DELTA-1-methyltestosterone (TURINABOL RTA), a new effective oral anabolic steroid.] Dtsch Gesundheitsw. 1965 Apr 15; 20:670-4. German. No abstract available. Bauersfeld K-H. OLEK Meibner J. H. D. Hannemann J. Spenke Analysis u. Einsatz des Mr. leichtathletischen In den Wurf / Stobie Disziplinen-und Versuch trainingsmethodischer Abteilungen und Verallgemeinerungen. Science Center DVfl 1973:41 pp. Clinical Chemistry 43:7. 1262-1279 (1997)
Oral Turinabol was first developed by scientists in East Germany for the Olympic athletes and national level for use. This, as well as possible to eliminate from the market caused OT to become very "sexy" for the athletes of drugs to try to get it. In East Germany, the drug studied in detail for many years, and some success in this country has now disappeared because of this drug, which made its first performance of athletes in the east of the Germany as little blue "Vitamins" their coaches gave them. This drug has been stopped at all the major pharmaceutical companies, but only through some underground laboratory. Although some sub-Labs have access to this issue and it appears on the lists of prices, it is still quite rare. I think this is the first time during the last decade and a half to a cat in Thailand. It is my hypothesis that the threshold of becoming very popular to the point where every Underground Lab will have its own version, or it will disappear, and then select only a few, if any suppliers. The easiest way to explain is that this drug is a derivative of Dianabol. Although it is a derivative of our old friend Diana, it is always ... Remember that balance is estrified Dianabol, and really has nothing to do with it, in terms of real-world implications. Take the OT with respect to the D-ball now, though. The first similarity between them is that they were both 17-alpha-alkylated (a carbon atom has been included in the 17th position) to survive the first pass through the liver. This, of course, increases hepatoxicity (liver toxicity). OT has a much lower level of activity compared to Dianabol androgens, but a better balance and the ratio of anabolic androgenic effects. It has a 0 rating (according to the Vida reference) for androgenic properties, steroids, and 53 for the properties on the basis of 100 points each for testosterone. This contributes to a more "rigid" Look, that competition bodybuilders often call "quality" muscle. You can not get the same "inflated" Look, how would you do with the D-bol, and many people in this way, compared to the results they have received from OT to Anavar. In reality, however, this material is simply Dianabol with 4-chloro changes, the same changes in clostebol. In this regard, the 4-chloro substitution in the A-ring Steran its Nucleus, the drug can not be aromatized (3). This, as you know, it is very useful and is one of the reasons Oral Turinabol been described as "gentle d-bol." You probably will not receive any estrogenic side effects like water retention, acne, gyno, etc, at a dose of the drug. Several studies I read examining male athletes over six weeks were given 10 mg OT / day did not show any signs of health danger. It is recommended that men should take between 20-40 mg per day, 5 mg and women every day, and I think in general it is not very strong (compared to many other oral) and not fall below 40 mg per Mark, if I had to use it personally. It May be used in low (ER) doses, if used only for its ability to reduce SHBG binding in (1) other steroids. In this regard, it May interact with other medicines, because it has the ability to reduce SHBG and thus free up more testosterone for use in your body. The only negative point that I heard of this drug is at high dose (10 + mg) virilization seen in women (14), and there was at least one case of testicular tumor, and one case of a guy who have suffered adverse effects from 5 years of use at high dose of P (2) (4). It should be noted that in the former East Germany has made a lot of experimentation with drugs in high doses, however, and found that it is a very suitable compound for their athletes. Many women suffered virilization at higher doses, however. During the 68-72 Olympic cycles, the East German Sports OT program made its biggest impact. At this time, East Germany took 10g/year weightlifters in overtime, as well as their main men took Sprinter 730mgs/year of OT (14). I think this tells me that for weight gains, and huge gains in the gym, you will need to break the bank of doses of this product. On the positive side, if you are a candidate for athletes faster, a little OT, it will be very quickly and with minimal (if any) side effects). I think the inability to cause negative side effects, and its ability to produce a favorable increase in lean body mass and thus a favorable increase in strength and speed and strength of an athlete: body ratio is the fact that transformed East Germany on the coaches and scientists. It should be noted that when this story is essentially undetectable, and this, of course, look for signs in the East Germans seeking to circumvent the testing procedures of drugs for the IOC. Now, of course, OT detected and after it is administered with a man, three major metabolites are formed: 6-beta-hydroxy-turinabol, 6 beta, 12-dihydroxy-turinabol and 6 beta, 16-dihydroxy - turinabol (5 ) (8) (9). All these metabolites are detectable drug screening. In many small amounts of at least three others are the excretion of metabolites, one of which is defined as May 17 epi-turinabol (5), which can be easily detected by testing modern ... No measurable OT is detected in any of urine proceedings against doping in sport, but the presence of metabolites sufficient for a positive result and a failed test. Keep all this in mind, it is important to note that the rate of metabolism and excretion of urine or oral Turinabol fast enough (5), although it is technically eliminated biphastically (in two parts) on the body, with the 16hr terminal half life (1). I think the sport of doping Poopers part (in the NCAA and IOC) OT is known to increase the time needed for your blood clot, as it is spontaneous fibrinolytic properties. "Fibrinolytic effects" means that the destruction of fibrin (insoluble fibrous protein produced in the liver of soluble protein) that occurs in your body. Fibrinogen is important in the process of blood clotting, as well as soluble proteins in the blood, which is converted into insoluble fibrin by the action of the enzyme thrombin in response to tissue damage. (6) (7) So you bleed longer than usual, when this material, combined with the fact that steroids raise your hematocrit and spend all morning trying to stop the bleeding, if you 're shaving. Well, this is probably an exaggeration, but not much. Oral Turinabol Olympic cycle I said that this story is a lean tissue builder, and good for cutting. But it is mainly of interest to bodybuilders. Now, with regard to athletics, the results can we expect? Well, I searched the literature in former East Germany, and found that they indicated that the number of world-class athletes are very clear improvement on the situation of at least 4 years of training period Olympic Men's Shot-putters were adding 2.5-4M shooting their free throws, 10-12M on their disk, and 6-10M with their Hammer throws. Female athletes gained even more. Let's look at the chart of improvements made by an individual, the strength of female athletes (* it has the world record shot put at the time of his departure OT administration), during the period of 18 to 13 July 1968 October, 1972. At that time he was in occupational therapy, has improved his throwing 18M 20m (yes, that is 2m + improvement, the world record of the Olympic Games while cycle). It takes about 5-15mgs/day of OT in the beginning, but 35mgs/day worked before she made her Olympic cycle. It throws while "OFF" OT even improved a little, leading to speculation that there are many successes to stand with the OT. Anyway, here in the admission patterns of OT, as well as improvements to this for 4 years, 4 years of her Olympic training regime: Effects on androgenic-anabolic steroid, Oral-Turinabol in the shot-put performance (in meters, the Y axis) of the female athlete (code identification 1 / 68 to 1 / 69 b, 1 / 72 c) directly photographed secret scientific report of Bauersfeld et al. (13) as one of the many documented examples, chosen because it is its historical significance as the first documented case of androgenic doping of a woman (for details see ref. (11)). (a) 1968. Rectangle from July 28 to 13 in October, said the period of drug administration, and the above figures show the daily number of tablets per week (in this case, 14 or 10 mg / day). The curve represents the results of competitions, an increase of the strength and performance of a fully trained woman. During the first use of drugs in 1968, athletes were well prepared for almost 14 years. Under the influence of drugs, however, she received an unprecedented number of improving muscle strength and records dramatically within a few weeks. (b) 1969. In the steroid was given in three cycles, and in various dosages, from 7 to 21 tablets per week (ie 5? 15 mg per day). Without the drugs, it can reach 18 meters, and when shooting drugs, she improved her world record once again at 20.10 h (C) 1972. It took even more of the hormone androgen, with daily doses of up to 7 pills a day (35 mg) in four cycles, for a total androgenic load of 1450 mg for one year. This led to the beginning of his speech within the winter season (left curve) and summer (right curve) and another staff (20.22 m). Pay attention to the significantly lower during the drug or after a short period of androgenization. In addition, after 4 years of systematic androgenization, its basic strength, even when not taking the drug also increased by ~ 1 m, indicative of a residual force. (14) Does all this work for those? Well, as I said earlier, almost everyone who took part in the Olympic program is German for steroids in one way or another, but the Old Testament was away, and most popular. They have access to some very strange, and too much testosterone intranasal, etc. And So ... Back to the Old Testament ... it differs from my testimony in this complex was that women are much more positive effect on OT than men (which applies to all steroids, though). In addition, women have more side effects, and generally have more serious side effects and unbearable than their male colleagues. Unfortunately, they also (sometimes), generally use higher doses than men, often up to 2x higher. Lets take a look at their type of doses per year: Some documents doses of anabolic-androgenic steroids (Oral-Turinabol) 1 adopted by the GDR medalists for women (athletics), the Olympic Games, World Championships and European Championships.2 (OT annual dose of MSG and events) 3680-Shot put 3190 Discus 2900-Shot put 2615-Shot put 2590-Shot put 1670 Sprint 1560 constraints 1480 constraints 1474 Sprint 1460 Sprint 1450-Shot put 1405 Sprint Heptathlon 1380 1375 Sprint Heptathlon 1340 1255 Discus Heptathlon 1230 1230 constraints 1185 javelin 1. Other esters of testosterone injections are not considered. 2. Data from ref. (14), which gives names and details. At least 12 of the drug-receiving competitors listed in the table of world records to save. In accordance with Journal policy regarding confidentiality of patients and subjects, the names of the elements were deleted. Shocked? Do not. It was during the Cold War and victory in the Olympic Games was seen as a victory for a certain lifestyle and certain ideologies, defeat is unthinkable and unacceptable. Does the recent resurgence of Oral-Turinabol on the black market will change in athletics and bodybuilding dramatically? № .. I doubt it ... combination of price ($ 1/10mgs average), and availability can lead to things that are undervalued tool at our disposal. However, it is a viable tool in weight of the meat-cutting cycle, cycle, or any athlete under drugs. In the finals, I'll give you an example (direct from the East German State Doping Program reports) on how they are used in the Old Testament, as well as several other drugs (eg, Prop. test by example): (Anabolic and special preparation for the commencement of the competition this year in direct training in the Olympic cycle 1980-84, for example, selected long jumpers (W) and high jumper (H) in conjunction with the results of competitions during this period) Example (from hundreds of evaluations) showing typical patterns oral administration of synthetic anabolic-androgenic steroids (Oral-Turinabol application period indicated by rectangles) and injections of testosterone ester [arrows, 10 mg propionate testosterone (TP), triangles, 25 mg of TP; circles, 100 mg of testosterone enanthate plus 1500 IU of hCG], here is a height (H) and long (W, Weitsprung) riders in the last 10 weeks before a major international competition in 1981? 1984 [immediate preparation period (UWV), in the week indicated on the X axis, a competition of the previous series UWV; competition results (in meters) above the drug application symbols]. (14) Oral Turinabol profile (4-chlorodehydromethyltestosterone) [4-chloro-17b-hydroxy-methyl-17A-androst-1 ,4-dien-3-one] Molecular Weight: 334.8854 Formula: C20H27O2Cl Manufacturer: Underground Labs only Effective Dose (men): 10-40mgs/day Effective Dose (Women): 5-15mgs/day Working life: 16 hours Detection time: 6 weeks Anabolic / Androgenic ratio:> 100:> 0 References: [The pharmacokinetics of Oral-Turinabol of Man] Pharmazie. 1991 Sep; 46 (9) :650-4. German. Department of Urology, Universitaetsklinikum "Carl Gustav Carus", Technical University of Dresden, Dresden, Germany 1-Effect of double bond and 11-beta-hydroxy group Stereospecific microbial reduction of 4-ene-3-oxo-steroids. J Steroid Biochem. October 1986, 25 (4) :561-6. Intratesticular leiomyosarcoma in a young man after high dose doping with Oral-Turinabol: case report. Cancer. 1999 Oct 15; 86 (8) :1571-5. GC capillary column and GC / MS for the determination of synthetic anabolic steroids. II. 4-chloro-methandienone (oral turinabol) and its metabolites. J Chromatogr Phys.-Math. 1983 Sep; 21 (9) :405-10. [Activation of the fibrinolytic system dehydrochlormethyltestosterone] Folia Haematol Int Mag Klin Morphol Blutforsch. 1984, 111 (4) :556-62. German. [Change hypofibrinolytic States dehydrochlormethyltestosterone] Folia Haematol Int Mag Klin Morphol Blutforsch. 1984, 111 (4) :563-6. German. [Application of microbial enzymes in studies of steroid substances (author's transl)] Acta Microbiol Acad Sciences Hung. 1975, 22 (4) :397-402. Review. German. [Application of microbial enzymes in studies of steroid substances (author's transl)] Acta Microbiol Acad Sciences Hung. 1975, 22 (4) :397-402. Review. German. [On the pharmacology "ORAL TURINABOL.] Dtsch Gesundheitsw. 1965 Apr 15; 20:690-1. German. No abstract available. Berendonk B. doping. Von der Forschung zum betrug. Reinbek bei Hamburg: Rowohlt Taschenbuchverlag. 1992:448 p. [4-CHLORO-DELTA-1-methyltestosterone (TURINABOL RTA), a new effective oral anabolic steroid.] Dtsch Gesundheitsw. 1965 Apr 15; 20:670-4. German. No abstract available. Bauersfeld K-H. OLEK Meibner J. H. D. Hannemann J. Spenke Analysis u. Einsatz des Mr. leichtathletischen In den Wurf / Stobie Disziplinen-und Versuch trainingsmethodischer Abteilungen und Verallgemeinerungen. Science Center DVfl 1973:41 pp. Clinical Chemistry 43:7. 1262-1279 (1997)
Orabolin (Ethylestranol)
Orabolin
(Ethylestranol) [19-Nor-17alpha-pregn-4-ene-17-PR] Formula: C20H22O Molecular Weight: 288.46 Melting point: 76-78C Manufacturer: Various, close Effective Dose (men): 40mg (?) Effective Dose (Women): 10mg (?) Active Life: 8-12 hours Detection time: 6 weeks Anabolic / Androgenic ratio (interval) :20-400 :200-400 What we'e here, looking at another steroid, which is to leave the market for so long that I could not actually find someone, who used it. This is a 19Nor-steroids, which means it has been received nandrolone. We always know that 19nor compounds bind to androgen receptors and that this is part of why he gave such an anabolic effect. It is very good, binding properties of androgens, which gives a good anabolic effect, but in fact reduced androgenically sensitive to androgens in the tissues of the prostate, and skin. There are few studies which considered the series to any depth, but those that I have read in fact, seem to indicate that it has an anabolic effect ethylestronol, making the 3-keto group and Indeed, the transition to norethandrolone (1). I think that is why it is very broad anabolic / androgenic range. There are also 17-alpha-ethyl group to resist, and that's what makes this complex hepatoxicity which makes the cost / benefit ratio is very bad for the athletes, so it is rare on the black market. In Orabolin the weirdest thing is that it is a strange pasta oral administrationâ € "I really do not know why this story ever put on the market, but the fact that it comes as an oral paste just very strange. Heres how ethylestranol metabolized in the body: Information: 1. The metabolism of anabolic steroids, human and marmoset monkeys (Callithrix jacchus) - I. Nilevar and Orabolin. J Steroid Biochem. October 1977, 8 (10) :1057-63.
(Ethylestranol) [19-Nor-17alpha-pregn-4-ene-17-PR] Formula: C20H22O Molecular Weight: 288.46 Melting point: 76-78C Manufacturer: Various, close Effective Dose (men): 40mg (?) Effective Dose (Women): 10mg (?) Active Life: 8-12 hours Detection time: 6 weeks Anabolic / Androgenic ratio (interval) :20-400 :200-400 What we'e here, looking at another steroid, which is to leave the market for so long that I could not actually find someone, who used it. This is a 19Nor-steroids, which means it has been received nandrolone. We always know that 19nor compounds bind to androgen receptors and that this is part of why he gave such an anabolic effect. It is very good, binding properties of androgens, which gives a good anabolic effect, but in fact reduced androgenically sensitive to androgens in the tissues of the prostate, and skin. There are few studies which considered the series to any depth, but those that I have read in fact, seem to indicate that it has an anabolic effect ethylestronol, making the 3-keto group and Indeed, the transition to norethandrolone (1). I think that is why it is very broad anabolic / androgenic range. There are also 17-alpha-ethyl group to resist, and that's what makes this complex hepatoxicity which makes the cost / benefit ratio is very bad for the athletes, so it is rare on the black market. In Orabolin the weirdest thing is that it is a strange pasta oral administrationâ € "I really do not know why this story ever put on the market, but the fact that it comes as an oral paste just very strange. Heres how ethylestranol metabolized in the body: Information: 1. The metabolism of anabolic steroids, human and marmoset monkeys (Callithrix jacchus) - I. Nilevar and Orabolin. J Steroid Biochem. October 1977, 8 (10) :1057-63.
Omnadren
Omnadren
(testosterone) Omnadren 250 is a combination of 4 tests esters above. Older versions of the list of drugs in the past two esters as isohexanoate and hexanoate. "However, it should be noted that hexanoate is simply another word for caproate esters because the drug is not altered. Most often, people will correlate Omnadren 250 with its once kidnapped brother, Sustanon 250, as they represent a mixture of esters of 4 test. The only difference between them lies in the last and most concentrated-ester. Although Omnadren contains caproate ester, Sustanon contains the decanoate ester in the same concentration. With the exception of prices, there is no difference and prices, and wise, you must pay for both ½ Omnadren and Sustanon for (or $ 3-4usd/amp). This is a very good price, and for this reason that I tend to advise people to buy more Omnadren Sustanon, if it is their source. In addition, it is not uncommon to hear people refer to Omnadren as the head version of testosterone, as it has 4 esters instead of 1 (or not). This should be taken with a grain of salt. All testosterone production very similar results, although the ester simply delays the release of the compound in the body, which has two immediate effects. The first, less important, is the frequency of injections. It is a highly controversial issue, and last, on the one hand are those who advocate injections once or twice a week. Often their arguments are supported with the results of the cycle, which allowed "good progress". On the other hand? and perhaps more scientific side are those who advocate the injection of at least once a day (EOD) or every day (ED). A single glance of the air in the constitution Omnadren can understand why it can be. These low concentrations of shorter esters (propionate and phenylpropionate) are practically useless when Omnadren is introduced once or twice a week. In addition, when injecting only a few times a week "peaks and valleys of the concentration in the blood are not desirable. We want the blood concentration of the drug are higher than they could be? Compared the dose, as long as possible. Obviously, this is not the case when rapid ester are introduced, then dispersed before an injection is given. As the ester in Omnadren (caproate) is slightly faster than the longest being distributed Sustanon (decanoate), users of their notice of increase in the level of testosterone and faster than Omnadren Sustanon. This has several consequences, which we will discuss today. First, because testosterone aromatization (conversion) to estrogen, and the accumulation of this female hormone will be faster. With estrogen increase follows the inevitability of growth retention. This is important for 3 reasons: first, the user is indeed increasing. Secondly, the size of users increases, and finally, the definition in the muscles begin dispersing. As an obvious consequence, Omnadren, usually used for bulking than cutting. The magnitude of this impact is largely dictated by the user of the diet and training habits, but it is also easy to control the proper use of anti-drugs such as estrogen Nolvadex, Armidex, and many Proviron others. As I said earlier, testosterone is highly anabolic and androgenic hormones, which is anabolic (bodybuilding) 100 rating, making it a good drug to use if the desire for more size and strength. And if you can not reach a greater size and strength, so why would you be reading this right? Well, let him see what makes a good mass builder testosterone. Firstly, testosterone promotes nitrogen retention in muscle (6) more nitrogen the muscles holds the more protein muscle stores. Testosterone May also greatly enhance the anabolic hormone, IGF-1 in muscle tissue (7) (9). Even the aromatized part of which converts testosterone into estrogen May increase the level of IGF, and sensitivity to it. Testosterone acts primarily by binding to androgen receptor of RA dependent mechanisms to promote muscle and fat loss (5). Fortunately, it also significantly increases the concentration of A. R in cells important for muscle repair and growth in the muscle and AR (8). Testosterone is changing the shape, size, and can also change the appearance and number of muscle fibers (7). Androgens, like testosterone (s) found in Omnadren can protect your hard earned muscle from catabolic hormones (8), if these hormones are derived from the exercise or other stress. Omnadren Side Effects There is a strong androgenic side effects, which are manufactured with Omnadren (as with all testosterone). Oily skin, acne, growth of body / face, and according to the increase in aggressiveness can occur. Omnadren can also be the hair. This is partly due to the conversion of testosterone into dihydrotestosterone (DGT). The test is converted to DHT via 5-alpha reductase enzyme. While the DGT is more powerful than the test on the androgen receptor (the double bond is removed from the carbon4-carbon5 duties and replaced by a hydrogen atom on each) and is responsible for growth. It can also cause negative effects as well. Testosterone under these obligations far more anabolic, a practical point of view, because, for example: the formation of DHT in the scalp is suspected of causing / accelerating baldness among men. To fight against this phenomenon, perhaps, can be used finasteride (Proscar ®). This drug inhibits the conversion of testosterone to TMD, but many users report that the DGT is more powerful in the androgen receptor test, gains in muscle mass and strength will be reduced. On the other hand, the lack of DHT caused by blocking 5-AR can sometimes cause gynocomastia (4) (5). Omnadren Cycles Usually, the cycles which contain Omnadren 250 will be about 12-16 weeks. The idea is that it takes at least 2 weeks in the complex is fully "active" in the body, and most users, a ratio of 1-3 weeks before the effects of Omnadren really felt. Accordingly, the benefit of Omnadren are not noticed, in general, about 1 month after the first injection. What most people remember that, although the drug is already active, gains are not realized immediately. Most users complete the quick action of oral drugs such as Dianabol or Anadrol for the first cycle of 4 weeks, which is considered a "kickstart" until the effects on the Omnadren are fully felt . As mentioned above, the typical weekly dose of Omnadren can range 500-1000mg per week. Those who are new to steroids and cycling should generally start with the minimum dose to better judge their own body responds to testosterone synthesis. I think beginners Stick 2 amps a week when they are inclined to use this drug. Omnadren always produced Polfa © which has since changed its name to Jelfa ©. The company is based in Poland, as one might conclude, of course, the availability and price of Omnadren 250 differs greatly from many other places. Sustanon is often forged in the 80s in fact prove Omnadren, which was much lower value (nonsensically). Omnadren (testosterone) Profile 1 ml Omnadren 250 contains: 30 mg of testosterone propionate 60 mg testosterone phenylpropionate 60 mg of testosterone isocaproate 100 mg of testosterone caproate [4-androstene-3-one-17beta-OL] 17beta-hydroxy-androst-4-ene-3-one Molecular Weight (base): 288,429 Molecular Weight (ester) Propionate: 362.5082 Phenylpropionate: 438.6058 Isocaproate: 404.5886 Caproate: 116.16 Formula (base): C19 H28 O2 Formula (ester) Propionate: C3 H6 O2 Phenylpropionate: C9 H10 O2 Isocaproate: C6 H12 O2 Caproate: C16 H12 O2 Melting point: 154-155C Manufacturer: Jelfa Effective dose: 250-1,000 MSG / week Working life: 10 days Detection time: 3 months Anabolic / Androgenic Ratio: 100:100 References: Hypothalamic sites of action of testosterone, dihydrotestosterone, and estrogen in regulating the secretion of luteinizing hormone human sheep. Endocrinology. 1997 Sep; 138 (9) :3686-94. The inhibition of LH secretion Localized administration of estrogen but not dihydrotestosterone, increased in the ventromedial hypothalamus Feed Restriction on young weather. Biol Reprod. 2005 Jun 22; [Epub ahead of print] Crystalline dihydrotestosterone implants in the lateral septum male rats. The positive effect of LH and FSH. Endocr Res. February-May 2001, 27 (1-2) :35-40. An important role of 5-alpha-reductase on feedback effects of androgens in cells of rat anterior pituitary gland demonstrated with a nonsteroidal 5 alpha-reductase inhibitor ONO-3805. J Androl. 1994 Nov-Dec; 15 (6) :521-7. CAS: Finasteride caused gynecomastia in the 62-year-old man. Am J Med Phys.-Math. June 1995, 309 (6) :322-5. J Clin Endocrinol Metab. 1997 Feb 82 (2) :407-13. Am J Physiol Endocrinol Metab. 2002 Mar; 282 (3): E601-7. Currency rating Clin Nutr Metab Care. May 2004, 7 (3) :271-7. Comparison of effects of increased serum levels of testosterone in the raloxifene and oral testosterone in serum insulin-like growth factor-1 and insulin like growth factor binding protein-3. Maturitas. 16 July 2005, 51 (3) :286-93.
(testosterone) Omnadren 250 is a combination of 4 tests esters above. Older versions of the list of drugs in the past two esters as isohexanoate and hexanoate. "However, it should be noted that hexanoate is simply another word for caproate esters because the drug is not altered. Most often, people will correlate Omnadren 250 with its once kidnapped brother, Sustanon 250, as they represent a mixture of esters of 4 test. The only difference between them lies in the last and most concentrated-ester. Although Omnadren contains caproate ester, Sustanon contains the decanoate ester in the same concentration. With the exception of prices, there is no difference and prices, and wise, you must pay for both ½ Omnadren and Sustanon for (or $ 3-4usd/amp). This is a very good price, and for this reason that I tend to advise people to buy more Omnadren Sustanon, if it is their source. In addition, it is not uncommon to hear people refer to Omnadren as the head version of testosterone, as it has 4 esters instead of 1 (or not). This should be taken with a grain of salt. All testosterone production very similar results, although the ester simply delays the release of the compound in the body, which has two immediate effects. The first, less important, is the frequency of injections. It is a highly controversial issue, and last, on the one hand are those who advocate injections once or twice a week. Often their arguments are supported with the results of the cycle, which allowed "good progress". On the other hand? and perhaps more scientific side are those who advocate the injection of at least once a day (EOD) or every day (ED). A single glance of the air in the constitution Omnadren can understand why it can be. These low concentrations of shorter esters (propionate and phenylpropionate) are practically useless when Omnadren is introduced once or twice a week. In addition, when injecting only a few times a week "peaks and valleys of the concentration in the blood are not desirable. We want the blood concentration of the drug are higher than they could be? Compared the dose, as long as possible. Obviously, this is not the case when rapid ester are introduced, then dispersed before an injection is given. As the ester in Omnadren (caproate) is slightly faster than the longest being distributed Sustanon (decanoate), users of their notice of increase in the level of testosterone and faster than Omnadren Sustanon. This has several consequences, which we will discuss today. First, because testosterone aromatization (conversion) to estrogen, and the accumulation of this female hormone will be faster. With estrogen increase follows the inevitability of growth retention. This is important for 3 reasons: first, the user is indeed increasing. Secondly, the size of users increases, and finally, the definition in the muscles begin dispersing. As an obvious consequence, Omnadren, usually used for bulking than cutting. The magnitude of this impact is largely dictated by the user of the diet and training habits, but it is also easy to control the proper use of anti-drugs such as estrogen Nolvadex, Armidex, and many Proviron others. As I said earlier, testosterone is highly anabolic and androgenic hormones, which is anabolic (bodybuilding) 100 rating, making it a good drug to use if the desire for more size and strength. And if you can not reach a greater size and strength, so why would you be reading this right? Well, let him see what makes a good mass builder testosterone. Firstly, testosterone promotes nitrogen retention in muscle (6) more nitrogen the muscles holds the more protein muscle stores. Testosterone May also greatly enhance the anabolic hormone, IGF-1 in muscle tissue (7) (9). Even the aromatized part of which converts testosterone into estrogen May increase the level of IGF, and sensitivity to it. Testosterone acts primarily by binding to androgen receptor of RA dependent mechanisms to promote muscle and fat loss (5). Fortunately, it also significantly increases the concentration of A. R in cells important for muscle repair and growth in the muscle and AR (8). Testosterone is changing the shape, size, and can also change the appearance and number of muscle fibers (7). Androgens, like testosterone (s) found in Omnadren can protect your hard earned muscle from catabolic hormones (8), if these hormones are derived from the exercise or other stress. Omnadren Side Effects There is a strong androgenic side effects, which are manufactured with Omnadren (as with all testosterone). Oily skin, acne, growth of body / face, and according to the increase in aggressiveness can occur. Omnadren can also be the hair. This is partly due to the conversion of testosterone into dihydrotestosterone (DGT). The test is converted to DHT via 5-alpha reductase enzyme. While the DGT is more powerful than the test on the androgen receptor (the double bond is removed from the carbon4-carbon5 duties and replaced by a hydrogen atom on each) and is responsible for growth. It can also cause negative effects as well. Testosterone under these obligations far more anabolic, a practical point of view, because, for example: the formation of DHT in the scalp is suspected of causing / accelerating baldness among men. To fight against this phenomenon, perhaps, can be used finasteride (Proscar ®). This drug inhibits the conversion of testosterone to TMD, but many users report that the DGT is more powerful in the androgen receptor test, gains in muscle mass and strength will be reduced. On the other hand, the lack of DHT caused by blocking 5-AR can sometimes cause gynocomastia (4) (5). Omnadren Cycles Usually, the cycles which contain Omnadren 250 will be about 12-16 weeks. The idea is that it takes at least 2 weeks in the complex is fully "active" in the body, and most users, a ratio of 1-3 weeks before the effects of Omnadren really felt. Accordingly, the benefit of Omnadren are not noticed, in general, about 1 month after the first injection. What most people remember that, although the drug is already active, gains are not realized immediately. Most users complete the quick action of oral drugs such as Dianabol or Anadrol for the first cycle of 4 weeks, which is considered a "kickstart" until the effects on the Omnadren are fully felt . As mentioned above, the typical weekly dose of Omnadren can range 500-1000mg per week. Those who are new to steroids and cycling should generally start with the minimum dose to better judge their own body responds to testosterone synthesis. I think beginners Stick 2 amps a week when they are inclined to use this drug. Omnadren always produced Polfa © which has since changed its name to Jelfa ©. The company is based in Poland, as one might conclude, of course, the availability and price of Omnadren 250 differs greatly from many other places. Sustanon is often forged in the 80s in fact prove Omnadren, which was much lower value (nonsensically). Omnadren (testosterone) Profile 1 ml Omnadren 250 contains: 30 mg of testosterone propionate 60 mg testosterone phenylpropionate 60 mg of testosterone isocaproate 100 mg of testosterone caproate [4-androstene-3-one-17beta-OL] 17beta-hydroxy-androst-4-ene-3-one Molecular Weight (base): 288,429 Molecular Weight (ester) Propionate: 362.5082 Phenylpropionate: 438.6058 Isocaproate: 404.5886 Caproate: 116.16 Formula (base): C19 H28 O2 Formula (ester) Propionate: C3 H6 O2 Phenylpropionate: C9 H10 O2 Isocaproate: C6 H12 O2 Caproate: C16 H12 O2 Melting point: 154-155C Manufacturer: Jelfa Effective dose: 250-1,000 MSG / week Working life: 10 days Detection time: 3 months Anabolic / Androgenic Ratio: 100:100 References: Hypothalamic sites of action of testosterone, dihydrotestosterone, and estrogen in regulating the secretion of luteinizing hormone human sheep. Endocrinology. 1997 Sep; 138 (9) :3686-94. The inhibition of LH secretion Localized administration of estrogen but not dihydrotestosterone, increased in the ventromedial hypothalamus Feed Restriction on young weather. Biol Reprod. 2005 Jun 22; [Epub ahead of print] Crystalline dihydrotestosterone implants in the lateral septum male rats. The positive effect of LH and FSH. Endocr Res. February-May 2001, 27 (1-2) :35-40. An important role of 5-alpha-reductase on feedback effects of androgens in cells of rat anterior pituitary gland demonstrated with a nonsteroidal 5 alpha-reductase inhibitor ONO-3805. J Androl. 1994 Nov-Dec; 15 (6) :521-7. CAS: Finasteride caused gynecomastia in the 62-year-old man. Am J Med Phys.-Math. June 1995, 309 (6) :322-5. J Clin Endocrinol Metab. 1997 Feb 82 (2) :407-13. Am J Physiol Endocrinol Metab. 2002 Mar; 282 (3): E601-7. Currency rating Clin Nutr Metab Care. May 2004, 7 (3) :271-7. Comparison of effects of increased serum levels of testosterone in the raloxifene and oral testosterone in serum insulin-like growth factor-1 and insulin like growth factor binding protein-3. Maturitas. 16 July 2005, 51 (3) :286-93.
Nolvadex (tamoxifen citrate)
Nolvadex
(Tamoxifen citrate) Nolvadex and Gynocomastia This medicine is used as first line of defense against breast cancer. In the late 80's, Dan Duchaine speculated that May also be used by bodybuilders to halt the development of another type of tumor in the breast, Gynocomastia. He presented his finding to the community of users of steroids, such as "preparation" The issue of groundwater and updating of the Manual Steroid Newsletter (contest prep release actually 3 questions in one, for those who subscribed to the newsletter). Nolvadex is generally described in a number of ways: as a SERM (Selective Estrogen Receptor Modulator), and anti-estrogen (which is actually incorrect, as we shall see later) and, finally, that triphenylethylene. I Stick to Nolvadex SERM, because I have three options, it will happen with the right (as we all know that the call for an anti-estrogen wrong), and pronounce (as we know, that I have no idea how to say "triphenylethylene). Selective modulators of estrogen receptor (SERMs) act as estrogen receptor agonists or antagonists in the tissue on a selective basis, which allows us to see what this means for us and Nolvadex is actually quite few requests for the use of steroids athletes. First, is the most common use is to prevent gynocomastia. Nolvadex if it is genuinely competing for the receptor site in breast tissue, and binding to it. Thus, we can say with certainty that the effect of tamoxifen is to block estrogen receptors in breast tissue (1), particularly in light of whole-body estradiol increases with use of tamoxifen. Of course, if you are on a cycle which includes steroids which convert to estrogen, you are considering NOLVADEX May as a good choice to run with them. Nolvadex Cycle Nolvadex however, is not the most powerful other compounds may be used in a loop, but this is probably the safer it is not actually reduce estrogen in the body of estrogen floating around may have many benefits for muscle growth, and. Estrogen is also essential for the proper functioning of the immune system, and not only that, but your lipid profile (HDL and LDL) have also shown improvements in the administration of tamoxifen (4). Many bodybuilders use this material as part of the cycle, for medical services provided. But if you're ready for the bodybuilding contest, you must use the aspiring majority (if not all) of estrogen in the body. I am speculating that you can use the Nolvadex for most competitions preparation cycle, to maintain relatively good health, then switch to letrozole for the last 8 weeks. Nolvadex is also important in the use of steroids athletes. In hypogonadic NOLVADEX infertile men with light, the increase in serum LH, FSH, and most importantly, testosterone were observed, all (2) (3). The Best (rough) feel that I can give you my research is that Nolvadex 20mg to raise your testosterone levels about 150% (5) ... and this will, of course, lots of help post-conflict cycle. What this means for us is that if you take Nolvadex after the cycle when you try to raise the level of testosterone, LH, FSH, and the return to normal life, he will be greatly aid recovery. In fact, if I were limited to a single connection to the menu of the post-cycle recovery, Nolvadex would be my choice. If you want to compare should be 150mg of Clomid to respond to this type of terrain of testosterone, but also NOLVADEX a surge of LH (Leutenizing hormone) response to LHRL (5), after 6 weeks. Some of the most difficult to maintain relationships that are available today, will give you more "dry" Look, this can not NOLVADEX NOLVADEX just safer to use long (over 16 weeks) cycles. Nolvadex Side Effects Unfortunately, Nolvadex is not perfect. The anecdote, it was associated with reduced profitability in some bodybuilders. This is not due, as previously estimated, the reduction of estrogen (which is not), but rather the ability to possibly reduce IGF (Insulin-like growth factor), which is important for muscle growth. Internet to buy Nolvadex Personally, I have great success with NOLVADEX cycles as well as without, but I can certainly attest to its effectiveness in preventing gynocomastia. Back in the late 90s, I purchased 30 tabs of Nolvadex 10mg for $ 30, but recently I have found much less at various websites. That costs money. References: Pädiatrie klin. 1987 Nov-Dec; 199 (6) :389-91. Stimulation of calcitonin secretory capacity of growth in serum testosterone levels in men treated with tamoxifen. Int J Androl. December 1987, 10 (6) :747-51. Hormonal changes in tamoxifen treatment with their male idiopathic oligozoospermia Exp Clin Endocrinol. December 1988, 92 (2) :211-6. 2 Bruning PF, Bronfer JMG, Hart AAM, Jong-Bakker M, tamoxifen, serum lipoproteins and cardiovascular risk, Br J. Cancer October 1988, 58 (4) 497-9 Fertil Steril. 1978 Mar; 29 (3) :320-7.
(Tamoxifen citrate) Nolvadex and Gynocomastia This medicine is used as first line of defense against breast cancer. In the late 80's, Dan Duchaine speculated that May also be used by bodybuilders to halt the development of another type of tumor in the breast, Gynocomastia. He presented his finding to the community of users of steroids, such as "preparation" The issue of groundwater and updating of the Manual Steroid Newsletter (contest prep release actually 3 questions in one, for those who subscribed to the newsletter). Nolvadex is generally described in a number of ways: as a SERM (Selective Estrogen Receptor Modulator), and anti-estrogen (which is actually incorrect, as we shall see later) and, finally, that triphenylethylene. I Stick to Nolvadex SERM, because I have three options, it will happen with the right (as we all know that the call for an anti-estrogen wrong), and pronounce (as we know, that I have no idea how to say "triphenylethylene). Selective modulators of estrogen receptor (SERMs) act as estrogen receptor agonists or antagonists in the tissue on a selective basis, which allows us to see what this means for us and Nolvadex is actually quite few requests for the use of steroids athletes. First, is the most common use is to prevent gynocomastia. Nolvadex if it is genuinely competing for the receptor site in breast tissue, and binding to it. Thus, we can say with certainty that the effect of tamoxifen is to block estrogen receptors in breast tissue (1), particularly in light of whole-body estradiol increases with use of tamoxifen. Of course, if you are on a cycle which includes steroids which convert to estrogen, you are considering NOLVADEX May as a good choice to run with them. Nolvadex Cycle Nolvadex however, is not the most powerful other compounds may be used in a loop, but this is probably the safer it is not actually reduce estrogen in the body of estrogen floating around may have many benefits for muscle growth, and. Estrogen is also essential for the proper functioning of the immune system, and not only that, but your lipid profile (HDL and LDL) have also shown improvements in the administration of tamoxifen (4). Many bodybuilders use this material as part of the cycle, for medical services provided. But if you're ready for the bodybuilding contest, you must use the aspiring majority (if not all) of estrogen in the body. I am speculating that you can use the Nolvadex for most competitions preparation cycle, to maintain relatively good health, then switch to letrozole for the last 8 weeks. Nolvadex is also important in the use of steroids athletes. In hypogonadic NOLVADEX infertile men with light, the increase in serum LH, FSH, and most importantly, testosterone were observed, all (2) (3). The Best (rough) feel that I can give you my research is that Nolvadex 20mg to raise your testosterone levels about 150% (5) ... and this will, of course, lots of help post-conflict cycle. What this means for us is that if you take Nolvadex after the cycle when you try to raise the level of testosterone, LH, FSH, and the return to normal life, he will be greatly aid recovery. In fact, if I were limited to a single connection to the menu of the post-cycle recovery, Nolvadex would be my choice. If you want to compare should be 150mg of Clomid to respond to this type of terrain of testosterone, but also NOLVADEX a surge of LH (Leutenizing hormone) response to LHRL (5), after 6 weeks. Some of the most difficult to maintain relationships that are available today, will give you more "dry" Look, this can not NOLVADEX NOLVADEX just safer to use long (over 16 weeks) cycles. Nolvadex Side Effects Unfortunately, Nolvadex is not perfect. The anecdote, it was associated with reduced profitability in some bodybuilders. This is not due, as previously estimated, the reduction of estrogen (which is not), but rather the ability to possibly reduce IGF (Insulin-like growth factor), which is important for muscle growth. Internet to buy Nolvadex Personally, I have great success with NOLVADEX cycles as well as without, but I can certainly attest to its effectiveness in preventing gynocomastia. Back in the late 90s, I purchased 30 tabs of Nolvadex 10mg for $ 30, but recently I have found much less at various websites. That costs money. References: Pädiatrie klin. 1987 Nov-Dec; 199 (6) :389-91. Stimulation of calcitonin secretory capacity of growth in serum testosterone levels in men treated with tamoxifen. Int J Androl. December 1987, 10 (6) :747-51. Hormonal changes in tamoxifen treatment with their male idiopathic oligozoospermia Exp Clin Endocrinol. December 1988, 92 (2) :211-6. 2 Bruning PF, Bronfer JMG, Hart AAM, Jong-Bakker M, tamoxifen, serum lipoproteins and cardiovascular risk, Br J. Cancer October 1988, 58 (4) 497-9 Fertil Steril. 1978 Mar; 29 (3) :320-7.
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