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[[Category:096.52 Add To Cart Rivotril (Clonazepam) 2mg by Roche x 500 Strips (Shipping Included) £653.57 Add To Cart Rivotril (Clonazepam) 2mg by Roche x 50 Strips (Shipping Included) £117.71 Add To Cart Rivotril (Clonazepam) 2mg by Roche x 40 Strips (Shipping Included) £105.32 Add To Cart Rivotril (Clonazepam) 2mg by Roche x 30 Strips (Shipping Included) £92.93 Add To Cart Rivotril (Clonazepam) 2mg by Roche x 20 Strips (Shipping Included) £80.54 Add To Cart Rivotril (Clonazepam) 2mg by Roche x 10 Strips (Shipping Included) £68.15 Add To Cart Sustanon 250mg Organon Karachi Pakistan x 300 Amps (Shipping Included) £433.65 Add To Cart Ritalin 10mg by Novartis x 150 Tablets (Shipping Included) £92.93 Add To Cart Ritalin 10mg by Novartis x 120 Tablets (Shipping Included) £86.73 Add To Cart Ritalin 10mg by Novartis x 90 Tablets (Shipping Included) £80.54 Add To Cart Ritalin 10mg by Novartis x 60 Tablets (Shipping Included) £74.34 Add To Cart Kinz Nalbuphine 20mg From Sami x 100 Amps £185.85 Add To Cart Kinz Nalbuphine 20mg From Sami x 10 Amps £24.78 Add To Cart Nolvadex (Tamoxifen Citrate) 20mg by AstraZeneca Poland x 1 Strip £7.43 Add To Cart Cypionax (Testosterone Cypionate) 2ml by Body Research x 100 Amps (Shipping Included) £433.65 Add To Cart Anavar (Oxandrolone) 5mg x 50 Tablets by LA Pharma x 10 Packs (Shipping Included) £619.50 Add To Cart Anavar (Oxandrolone) 10mg x 30 Tablets by LA Pharma x 10 Packs (Shipping Included) £805.35 Add To Cart T3-Cytomel 100 mcg LA Pharma x 10 Bottles (Shipping Included) £309.75 Add To Cart Clenbuterol 20mcg x 10 Bottles (Shipping Included) £402.68 Add To Cart Cialis (Tadalifil Citrate) 20mg x 100 Blisters (Shipping Included) £433.65 Add To Cart Viagra (Sildenafil Citrate) 100mg by Pfizer x 100 Blisters (Shipping Included) £619.50 Add To Cart STEROIDS FOR SPORTS ENHANCEMENT For as long as athletic competition has existed men have experimented with food products]][[Category:but rather to equip them with the truth about anabolic steroids regarding their past and present roles in athletic performance enhancement. PERFORMANCE ENHANCEMENT HISTORY The story of steroid use in sports began just before the World Weightlifting Championships of 1954. The Soviets had made their Olympic debut in Helsinki in 1952]][[Category:and were only caught when word of them somehow leaked out. The Russians and Americans were also very successful at hiding usage. In the background professional bodybuildingmarched onward with competitors taking ever-increasing amounts of AAS and other drugs]][[Category:at least half the guys are using steroids. They talk about it. They joke about it with each other. The guys who want to protect themselves or their image by lying have that right. Me? I'm at the point in my career where I've done just about every bad thing you can do. I try to walk with my head up. I don't have to hold my tongue…" (p.36) - Ken Caminiti]][[Category:June 2002 Major League Baseball (MLB) was the last professional sports organization in the United States to implement a comprehensive drug testing policy. This all started when an over-the-counter nutritional supplement bottle was seen in Mark McGwire's locker. The bottle in question contained the prohormone Androstendione]][[Category:his story was followed by hundreds of mainstream media publications. The most famous AAS story in the in sports is that of Jason Giambi and Barry Bonds. Both of those players were suspected of using anabolic steroids when the BALCO scandal was exposed. Giambi told a U.S. grand jury that he used a duo of undetectable steroids known respectively as "the cream" and "the clear]][[Category:said the leak of the testimony was simply engineered to discredit Mr. Bonds. It is also important to note that none of these substances were banned by MLB at that time. So did all this media attention hurt baseball? The answer is a resounding "no". Baseball attendance was in a slump before McGwire was en route to his home-run record]][[Category:about AAS in Major League baseball. Do major league players use steroids? Of course they do! Can we say that steroids are the reason for the inflated home-run statistics of recent years? Of course not. With multi-million dollar contracts on the line every season]][[Category:but AAS use in baseball is unlikely to decline considerably as a result of this...there's just too much at stake! STEROIDS IN FOOTBALL The steroid policy in the National Football League (NFL) began in 1987. But to understand the use of steroids in football]][[Category:makes a strong case. Using this starting point we can better assess AAS use in professional football. So what does the landscape of professional football look like anyway? This storyline is very similar to that of the high school and collegiate ranks. For example]][[Category:and there was absolutely no reason for Alzado to believe his condition could have been attributed to his steroid use. He could just as easily have made the exact same evidence-free claim about his Gatorade drinking. The story of Bill Romanowski is probably the next most influential one concerning AAS in football. Although Romanowski wasn't indicted in the BALCO scandal]][[Category:Charlie Francis has provided ample evidence for the unreliability of the testing (3). Briefly he states that the accepted drug clearance time for Winstrol (at that time) was +/- three days for the oral form and +/- 14 days for the injectable. Ben had used the compound 28 days prior to the race]][[Category:and for her role in a check-fraud scam. The New York Times first reported that Marion has been working on her basketball skills and conditioning in San Antonio since October ‘08. Jones told the newspaper she received a call in May from someone in the NBA asking if she might play in the WNBA. "I thought it would be an interesting journey if I decided to do this]][[Category:where she was the starting point guard on the Tar Heels' National Championship Team in 1994. She told the Times that she hopes to play in Europe this winter and in the WNBA next season. I for one believe she deserves that second chance and I'll wish her well]][[Category:and colloquial usage.[3] In pharmacology]][[Category:or diagnosis of disease or used to otherwise enhance physical or mental well-being."[3] Drugs may be prescribed for a limited duration]]

[[Category:or on a regular basis for chronic disorders.[4] Recreational drugs are chemical substances that affect the central nervous system]] [[Category:such as opioids or hallucinogens.[4] They may be used for perceived beneficial effects on perception]][[Category:and behavior.[4][5] Some drugs can cause addiction and/or habituation.[5] Drugs are usually distinguished from endogenous biochemicals by being introduced from outside the organism.[citation needed] For example]][[Category:it is called a drug.[citation needed] Many natural substances]][[Category:as when ingested they affect the functioning of both mind and body and some substances normally considered drugs such as DMT (Dimethyltryptamine) are actually produced by the human body in trace amounts. Contents [hide] 1 Etymology 2 Medication 3 Spiritual and religious use 4 Self-improvement 5 Recreational drug use 6 Administering drugs 7 See also 8 References 9 External links Etymology Drug is thought to originate from Old French "drogue"]][[Category:referring to medicinal plants preserved in them.[6] Medication Nexium pills 40 mg (esomeprazole magnesium) Main article: pharmaceutical drug A medication or medicine is a drug taken to cure and/or ameliorate any symptoms of an illness or medical condition]][[Category:usually a physician.[citation needed] In the United Kingdom]][[Category:by or under the supervision of a pharmacist. These medications are designated by the letter P on the label.[7] The range of medicines available without a prescription varies from country to country. Medications are typically produced by pharmaceutical companies and are often patented to give the developer exclusive rights to produce them. Those that are not patented (or with expired patents) are called generic drugs since they can be produced by other companies without restrictions or licenses from the patent holder. Spiritual and religious use Main article: Entheogen The spiritual and religious use of drugs has been occurring since the dawn of our species. Drugs that are considered to have spiritual or religious use are called entheogens. Some religions are based completely on the use of certain drugs. Entheogens are mostly hallucinogens]][[Category:often by professional athletes. Recreational drug use The cigarette is the common pharmaceutical form of tobacco – one of the world’s best selling drugs.[8] Cannabis is another commonly used recreational drug.[9] Ayahuasca Main article: Recreational drug use Further information: Prohibition of drugs Recreational drugs use is the use of psychoactive substances to have fun]][[Category:or to enhance an already positive experience. National laws prohibit the use of many different recreational drugs and medicinal drugs that have the potential for recreational use are heavily regulated. Many other recreational drugs on the other hand are legal]][[Category:usually as a cream or ointment. A drug administered in this manner may be given to act locally or systemically.[10] Vaginally as a suppository]] [[Category:primarily to treat vaginal infections. See also Pharmacy and Pharmacology portal Drug development Drug injection Inverse benefit law Lifestyle drug List of drugs List of pharmaceutical companies List of psychedelic plants Placebo Prodrug United Nations Office on Drugs and Crime References ^ Deutscher Kaffeeverband (2001-05-04). "Kaffee-Text 1/99" (in German) (PDF). Archived from the original on 2008-02-29. Retrieved 2007-12-14. ^ In Germany about 118 l of beer]][[Category:4 l of sparkling wine and 6 l of distilled beverages are consumed per person per year.[citation needed] ^ a b "Drug." Dictionary.com Unabridged (v 1.1)]][[Category:Douglas. "drug". Online Etymology Dictionary. ^ "Glossary of MHRA terms - P". MHRA. Retrieved 2008-11-05. ^ According to the statistic of the Food and Agriculture Organization the production quantity in 2006 of coffee was 7.8 million tonnes and of tobacco was 6.7 million tonnes. ^ Lingeman]][[Category:with a hydroxyl group at position-3 and a skeleton derived from cholestane.[1] Hundreds of distinct steroids are found in plants]][[Category:and fungi. All steroids are made in cells either from the sterols lanosterol (animals and fungi) or from cycloartenol (plants). Both lanosterol and cycloartenol are derived from the cyclization of the triterpene squalene.[2] Contents [hide] 1 Structure 2 Classification 2.1 Taxonomical/functional 2.2 Structural 3 Biosynthesis 3.1 Mevalonate pathway 3.1.1 Pharmacology 3.2 DMAPP to lanosterol 3.3 Steroidogenesis 3.4 Regulation 3.5 Alternative pathways 4 Metabolism 5 See also 6 References 7 External links [edit]Structure Steroids are a class of organic compounds with a chemical structure that contains the core of gonane or a skeleton derived therefrom. Usually]][[Category:together they are called cyclopentaphenanthrene.[3] Numbering of rings and of carbon atoms in gonane]][[Category:a phytosterol showing the hydroxyl group at C-3. [edit]Classification [edit]Taxonomical/functional Some of the common categories of steroids: Animal Insect Ecdysteroids such as ecdysterone that controls moulting Vertebrate Steroid hormones Sex steroids are a subset of sex hormones that produce sex differences or support reproduction. They include androgens]][[Category:whereas mineralocorticoids help maintain blood volume and control renal excretion of electrolytes. Most medical 'steroid' drugs are corticosteroids. Anabolic steroids are a class of steroids that interact with androgen receptors to increase muscle and bone synthesis. There are natural and synthetic anabolic steroids. In popular language]][[Category:which modulates the fluidity of cell membranes and is the principal constituent of the plaques implicated in atherosclerosis. Plant Phytosterols Brassinosteroids (includes several plant hormones) Fungus Ergosterols [edit]Structural It is also possible to classify steroids based upon their chemical composition. One example of how MeSH performs this classification is available at the Wikipedia MeSH catalog. Examples from this classification include: Class Examples Number of carbon atoms Cholestanes cholesterol 27 Cholanes cholic acid 24 Pregnanes progesterone 21 Androstanes testosterone 19 Estranes estradiol 18 Gonane (or steroid nucleus) is the parent (17-carbon tetracyclic) hydrocarbon molecule without any alkyl sidechains.[4] [edit]Biosynthesis Steroid biosynthesis is an anabolic metabolic pathway that produces steroids from simple precursors. A unique biosynthetic pathway is followed in animals compared to many other organisms]][[Category:the biosynthesis of steroids follows the mevalonate pathway that uses acetyl-CoA as building-blocks to form dimethylallyl pyrophosphate (DMAPP) and isopentenyl pyrophosphate (IPP).[5] In subsequent steps]][[Category:which in turn is used to synthesize the steroid lanosterol. Further modifications of lanosterol into other steroids are classified steroidogenesis transformations. [edit]Mevalonate pathway Main article: Mevalonate pathway The mevalonate pathway or HMG-CoA reductase pathway starts with and ends with dimethylallyl pyrophosphate (DMAPP) and isopentenyl pyrophosphate (IPP). Mevalonate pathway [edit]Pharmacology A number of drugs target the mevalonate pathway: Statins (used for elevated cholesterol levels) Bisphosphonates (used in treatment of various bone-degenerative diseases) [edit]DMAPP to lanosterol Isopentenyl pyrophosphate and dimethylallyl pyrophosphate donate isoprene units]][[Category:[6] which are a large class of lipids that include the carotenoids]] [[Category:and form the largest class of plant natural products.[7] Here]] [[Category:the isoprene units are joined together to make squalene and then folded up and formed into a set of rings to make lanosterol.[8] Lanosterol can then be converted into other steroids such as cholesterol and ergosterol.[8][9] [edit]Steroidogenesis "Steroidogenesis" redirects here. Steroidogenesis is the biological process by which steroids are generated from cholesterol and transformed into other steroids.[10] The pathways of steroidogenesis differ between different species – as an example the pathways of human steroidogenesis are shown in this figure below: The human steroidogenesis]][[Category:individual steroids and enzymatic pathways. Note that changes in molecular structure compared to the respective precursor are highlighted with white circles. The major classes of steroid hormones and some prominent members of the human steroidogenesis are: Progestogens: Progesterone Corticosteroids (Corticoids): Aldosterone (Mineralocorticoids) Cortisol (Glucocorticoids) Androgens: Testosterone Estrogens: Estrogen Locations of human steroidogenesis: Progestogens serve as precursors to all other human steroids – thus all human tissues which produce steroids must first convert cholesterol to pregnenolone. This conversion is the rate-limiting step of steroid synthesis]] [[Category:which occurs inside the mitochondrion of the respective tissue.[11] Corticosteroids are produced in the adrenal cortex. Estrogen and progesterone are made primarily in the ovary and in the placenta during pregnancy]][[Category:either de novo or from peripherally-derived sources. [edit]Regulation Several key enzymes can be activated through DNA transcriptional regulation on activation of SREBP (Sterol Regulatory Element-Binding Protein-1 and -2). This intracellular sensor detects low cholesterol levels and stimulates endogenous production by the HMG-CoA reductase pathway]][[Category:degradation of reductase and phosphorylation. [edit]Alternative pathways In plants and bacteria]] [[Category:the non-mevalonate pathway uses pyruvate and glyceraldehyde 3-phosphate as substrates.[6][12] [edit]Metabolism Steroids are oxidized mainly by cytochrome P450 oxidase enzymes]][[Category:to form bile acids as final products.[13] These bile acids can then be eliminated through secretion from the liver in the bile.[14] The expression of this oxidase gene can be upregulated by the steroid sensor PXR when there is a high blood concentration of steroids.[15] [edit]See also pharmacology portal Batrachotoxin List of steroid abbreviations Steroid hormone Corticosteroid Sex steroid Steroid sulfatase Steroid hydroxylases Steroidogenic acute regulatory protein [edit]References ^ a b G. P. Moss (1989). "Nomenclature of Steroids (Recommendations 1989)". Pure & Appl. Chem. 61 (10): 1783–1822. doi:10.1351/pac198961101783. PDF "IUPAC-IUB Joint Commission on Biochemical Nomenclature (JCBN). The nomenclature of steroids. Recommendations 1989". Eur. J. Biochem. 186 (3): 429–58. December 1989. doi:10.1111/j.1432-1033.1989.tb15228.x. PMID 2606099. ^ "Lanosterol biosynthesis". Recommendations on Biochemical & Organic Nomenclature]][[Category:Luthra R (2003). "An overview of the non-mevalonate pathway for terpenoid biosynthesis in plants". J Biosci 28 (5): 637–46. doi:10.1007/BF02703339. PMID 14517367. ^ a b Schroepfer G (1981). "Sterol biosynthesis". Annu Rev Biochem 50: 585–621. doi:10.1146/annurev.bi.50.070181.003101. PMID 7023367. ^ Lees N]][[Category:and role in regulation of steroid hormone biosynthesis.". J Steroid Biochem Mol Biol 43 (8): 779–804. doi:10.1016/0960-0760(92)90307-5. PMID 22217824. ^ Rossier MF (2006). "T channels and steroid biosynthesis: in search of a link with mitochondria". Cell Calcium. 40 (2): 155–64. doi:10.1016/j.ceca.2006.04.020. PMID 16759697. ^ Lichtenthaler H (1999). "The 1-Dideoxy-D-xylulose-5-phosphate pathway of isoprenoid biosynthesis in plants". Annu Rev Plant Physiol Plant Mol Biol 50: 47–65. doi:10.1146/annurev.arplant.50.1.47. PMID 15012203. ^ Pikuleva IA (2006). "Cytochrome P450s and cholesterol homeostasis". Pharmacol. Ther. 112 (3): 761–73. doi:10.1016/j.pharmthera.2006.05.014. PMID 16872679. ^ Zollner G]][[Category:and that the gains in muscular strength achieved through high-intensity exercise and proper diet can be additionally increased by the use of AAS in some individuals.[1] Health risks can be produced by long-term use or excessive doses of anabolic steroids.[2][3] These effects include harmful changes in cholesterol levels (increased low-density lipoprotein and decreased high-density lipoprotein)]][[Category:dangerous changes in the structure of the left ventricle of the heart.[4] Conditions pertaining to hormonal imbalances such as gynecomastia and testicular atrophy may also be caused by anabolic steroids. Ergogenic uses for anabolic steroids in sports]][[Category:AAS have been by far the most detected doping substances in IOC-accredited laboratories.[5][6] In countries where AAS are controlled substances]][[Category:or even counterfeit drugs are sold to users. Contents [hide] 1 History 1.1 Isolation of gonadal AAS 1.2 Development of synthetic AAS 2 Pharmacology 2.1 Routes of administrations 2.2 Mechanism of action 2.3 Anabolic and androgenic effects 2.3.1 Body composition and strength improvements 3 Adverse effects 3.1 Psychiatric effects 3.2 Aggression and hypomania 3.3 Depression and suicide 3.4 Addiction potential 4 Medical and ergogenic uses 4.1 Medical uses 4.2 Ergogenic use and abuse 5 Legal and sport restrictions 5.1 Legal status 5.1.1 United States 5.1.2 United Kingdom 5.2 Status in sports 5.3 Detection of use 6 Illegal trade 7 See also 8 References 9 Further reading 10 External links [edit]History [edit]Isolation of gonadal AAS Chemical structure of the natural anabolic hormone testosterone]] [[Category:17β-hydroxy-4-androsten-3-one The use of gonadal steroids pre-dates their identification and isolation. Medical use of testicle extract began in the late 19th century while its effects on strength were still being studied.[7] The isolation of gonadal steroids can be traced back to 1931]][[Category:a chemist in Zurich.[8] In the 1930s]][[Category:raced to isolate it.[8][9] This hormone was first identified by Karoly Gyula David]][[Category:J. Freud and Ernst Laqueur in a May 1935 paper "On Crystalline Male Hormone from Testicles (Testosterone)."[10] They named the hormone testosterone]][[Category:when Butenandt and G. Hanisch published a paper describing "A Method for Preparing Testosterone from Cholesterol."[11] Only a week later]][[Category:announced a patent application in a paper "On the Artificial Preparation of the Testicular Hormone Testosterone (Androsten-3-one-17-ol)."[12] Ruzicka and Butenandt were offered the 1939 Nobel Prize in Chemistry for their work]][[Category:although he accepted the prize after the end of World War II.[8][9] Clinical trials on humans]][[Category:began as early as 1937.[8] Testosterone propionate is mentioned in a letter to the editor of Strength and Health magazine in 1938; this is the earliest known reference to an anabolic steroid in a U.S. weightlifting or bodybuilding magazine.[8] There are often reported rumors that German soldiers were administered anabolic steroids during the Second World War]][[Category:unproven.[13] Adolf Hitler himself]][[Category:was injected with testosterone derivatives to treat various ailments.[14] AAS were used in experiments conducted by the Nazis on concentration camp inmates]] [[Category:[14] and later by the allies attempting to treat the malnourished victims that survived Nazi camps.[13] President John F. Kennedy was administered steroids both before and during his presidency.[15] [edit]Development of synthetic AAS Chemical structure of the synthetic steroid Methandrostenolone (Dianabol). 17α-Methylation (upper-right corner) enhances oral bioavailability. The development of muscle-building properties of testosterone was pursued in the 1940s]][[Category:the U.S. Olympic Team physician Dr. John Ziegler worked with synthetic chemists to develop an anabolic steroid with reduced androgenic effects.[16] Ziegler's work resulted in the production of methandrostenolone]] [[Category:which Ciba Pharmaceuticals marketed as Dianabol. The new steroid was approved for use in the U.S. by the Food and Drug Administration (FDA) in 1958. It was most commonly administered to burn victims and the elderly. The drug's off-label users were mostly bodybuilders and weight lifters. Although Ziegler prescribed only small doses to athletes]] [[Category:he soon discovered that those having abused Dianabol suffered from enlarged prostates and atrophied testes.[17] AAS were placed on the list of banned substances of the IOC in 1976]] [[Category:and a decade later the committee introduced 'out-of-competition' doping tests because many athletes used AAS in their training period rather than during competition.[5] Three major ideas governed modifications of testosterone into a multitude of AAS: Alkylation at 17-alpha position with methyl or ethyl group created orally active compounds because it slows the degradation of the drug by the liver; esterification of testosterone and nortestosterone at the 17-beta position allows the substance to be administered parenterally and increases the duration of effectiveness because agents soluble in oily liquids may be present in the body for several months; and alterations of the ring structure were applied for both oral and parenteral agents to seeking to obtain different anabolic to androgenic effect ratios.[18] [edit]Pharmacology [edit]Routes of administrations A vial of injectable testosterone cypionate There are four common forms in which anabolic steroids are administered: oral pills]][[Category:but medical injections are normally done anywhere between semi-weekly to once every 12 weeks. A more frequent schedule may be desirable in order to maintain a more constant level of hormone in the system.[19] Injectable steroids are typically administered into the muscle]][[Category:intravenous injection has the potential to cause a dangerous embolism (clot) in the bloodstream. Transdermal patches (adhesive patches placed on the skin) may also be used to deliver a steady dose through the skin and into the bloodstream. Testosterone-containing creams and gels that are applied daily to the skin are also available]][[Category:since the medication can be washed off and may take up to six hours to be fully absorbed. There is also the risk that an intimate partner or child may come in contact with the application site and inadvertently dose himself or herself; children and women are highly sensitive to testosterone and can suffer unintended masculinization and health effects]] [[Category:even from small doses. Injection is the most common method used by individuals administering anabolic steroids for non-medical purposes.[20] The traditional routes of administration do not have differential effects on the efficacy of the drug. Studies indicate that the anabolic properties of anabolic steroids are relatively similar despite the differences in pharmacokinetic principles such as first-pass metabolism. However]] [[Category:the orally available forms of AAS may cause liver damage in high doses.[6][21] [edit]Mechanism of action See also: Steroid hormone The human androgen receptor bound to testosterone[22] The protein is shown as a ribbon diagram in red]][[Category:with the steroid shown in white. The pharmacodynamics of anabolic steroids are unlike peptide hormones. Water-soluble peptide hormones cannot penetrate the fatty cell membrane and only indirectly affect the nucleus of target cells through their interaction with the cell’s surface receptors. However]][[Category:anabolic steroids are membrane-permeable and influence the nucleus of cells by direct action. The pharmacodynamic action of anabolic steroids begin when the exogenous hormone penetrates the membrane of the target cell and binds to an androgen receptor located in the cytoplasm of that cell. From there]][[Category:where it either alters the expression of genes[23] or activates processes that send signals to other parts of the cell.[24] Different types of anabolic steroids bind to the androgen receptor with different affinities]] [[Category:depending on their chemical structure.[5] Some anabolic steroids such as methandrostenolone bind weakly to this receptor in vitro]] [[Category:but still exhibit androgenic effects in vivo. The reason for this discrepancy is not known.[25] The effect of anabolic steroids on muscle mass is caused in at least two ways:[26] first]][[Category:so that catabolism of muscle is greatly reduced. It has been hypothesized that this reduction in muscle breakdown may occur through anabolic steroids inhibiting the action of other steroid hormones called glucocorticoids that promote the breakdown of muscles.[27] Anabolic steroids also affect the number of cells that develop into fat-storage cells]] [[Category:by favouring cellular differentiation into muscle cells instead.[28] Anabolic steroids can also decrease fat by increasing basal metabolic rate (BMR)]] [[Category:since an increase in muscle mass increases BMR. [edit]Anabolic and androgenic effects Relative androgenic:anabolic activity in animals[19] Preparation Ratio Testosterone 1:1 Methyltestosterone 1:1 Fluoxymesterone 1:2 Oxymetholone 1:3 Oxandrolone 1:3–1:13 Nandrolone decanoate 1:2.5–1:4 As the name suggests]][[Category:leading to increased strength.[29][30][31] The androgenic effects of AAS are numerous. Depending on the length of use]][[Category:and impaired production of sperm.[32] The androgenic:anabolic ratio of an AAS is an important factor when determining the clinical application of these compounds. Compounds with a high ratio of androgenic to an anabolic effects are the drug of choice in androgen-replacement therapy (e.g.]][[Category:where all anabolic steroids have significant androgenic effects.[19] A commonly used protocol for determining the androgenic:anabolic ratio]][[Category:while the LA weight is an indicator of the anabolic effect. Two or more batches of rats are castrated and given no treatment and respectively some AAS of interest. The LA/VP ratio for an AAS is calculated as the ratio of LA/VP weight gains produced by the treatment with that compound using castrated but untreated rats as baseline: (LAc]][[Category:which have their androgenic:anabolic ratios scaled accordingly (as shown in the table above).[25][33] In the early 2000s]] [[Category:this procedure was standardized and generalized throughout OECD in what is now known as the Hershberger assay. [edit]Body composition and strength improvements A review spanning more than three decades of experimental studies in men found that body weight may increase by 2–5 kg as a result of short-term (



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