Anabolic agents. Medical search

These compounds stimulate anabolism and inhibit catabolism. They stimulate the development of muscle mass, strength, and power.

A non-steroidal estrogen analog.

A synthetic estrogen that has been used as a hormonal antineoplastic agent.

An anabolic steroid used mainly as an anabolic agent in veterinary practice.

A synthetic hormone with anabolic and androgenic properties.

A polypeptide that consists of the 1-34 amino-acid fragment of human PARATHYROID HORMONE, the biologically active N-terminal region. The acetate form is given by intravenous infusion in the differential diagnosis of HYPOPARATHYROIDISM and PSEUDOHYPOPARATHYROIDISM. (Reynolds JEF(Ed): Martindale: The Extra Pharmacopoeia (electronic version). Micromedex, Inc, Englewood, CO, 1995)

Reduction of bone mass without alteration in the composition of bone, leading to fractures. Primary osteoporosis can be of two major types: postmenopausal osteoporosis (OSTEOPOROSIS, POSTMENOPAUSAL) and age-related or senile osteoporosis.

Bone-forming cells which secrete an EXTRACELLULAR MATRIX. HYDROXYAPATITE crystals are then deposited into the matrix to form bone.

A polypeptide hormone (84 amino acid residues) secreted by the PARATHYROID GLANDS which performs the essential role of maintaining intracellular CALCIUM levels in the body. Parathyroid hormone increases intracellular calcium by promoting the release of CALCIUM from BONE, increases the intestinal absorption of calcium, increases the renal tubular reabsorption of calcium, and increases the renal excretion of phosphates.

The continuous turnover of BONE MATRIX and mineral that involves first an increase in BONE RESORPTION (osteoclastic activity) and later, reactive BONE FORMATION (osteoblastic activity). The process of bone remodeling takes place in the adult skeleton at discrete foci. The process ensures the mechanical integrity of the skeleton throughout life and plays an important role in calcium HOMEOSTASIS. An imbalance in the regulation of bone remodeling's two contrasting events, bone resorption and bone formation, results in many of the metabolic bone diseases, such as OSTEOPOROSIS.

Agents that inhibit BONE RESORPTION and/or favor BONE MINERALIZATION and BONE REGENERATION. They are used to heal BONE FRACTURES and to treat METABOLIC BONE DISEASES such as OSTEOPOROSIS.

A specialized CONNECTIVE TISSUE that is the main constituent of the SKELETON. The principle cellular component of bone is comprised of OSTEOBLASTS; OSTEOCYTES; and OSTEOCLASTS, while FIBRILLAR COLLAGENS and hydroxyapatite crystals form the BONE MATRIX.

A synthetic nonsteroidal estrogen used in the treatment of menopausal and postmenopausal disorders. It was also used formerly as a growth promoter in animals. According to the Fourth Annual Report on Carcinogens (NTP 85-002, 1985), diethylstilbestrol has been listed as a known carcinogen. (Merck, 11th ed)

The process of bone formation. Histogenesis of bone including ossification.

The amount of mineral per square centimeter of BONE. This is the definition used in clinical practice. Actual bone density would be expressed in grams per milliliter. It is most frequently measured by X-RAY ABSORPTIOMETRY or TOMOGRAPHY, X RAY COMPUTED. Bone density is an important predictor for OSTEOPOROSIS.

Alterations in diaphragm contractility after nandrolone administration: an analysis of potential mechanisms. (1/470)

The aim of this study was to evaluate the potential mechanisms underlying the improved contractility of the diaphragm (Dia) in adult intact male hamsters after nandrolone (Nan) administration, given subcutaneously over 4 wk via a controlled-release capsule (initial dose: 4.5 mg. kg-1. day-1; with weight gain, final dose: 2.7 mg. kg-1. day-1). Control (Ctl) animals received blank capsules. Isometric contractile properties of the Dia were determined in vitro after 4 wk. The maximum velocity of unloaded shortening (Vo) was determined in vitro by means of the slack test. Dia fibers were classified histochemically on the basis of myofibrillar ATPase staining and fiber cross-sectional area (CSA), and the relative interstitial space was quantitated. Ca2+-activated myosin ATPase activity was determined by quantitative histochemistry in individual diaphragm fibers. Myosin heavy chain (MHC) isoforms were identified electrophoretically, and their proportions were determined by using scanning densitometry. Peak twitch and tetanic forces, as well as Vo, were significantly greater in Nan animals compared with Ctl. The proportion of type IIa Dia fibers was significantly increased in Nan animals. Nan increased the CSA of all fiber types (26-47%), whereas the relative interstitial space decreased. The relative contribution of fiber types to total costal Dia area was preserved between the groups. Proportions of MHC isoforms were similar between the groups. There was a tendency for increased expression of MHC2B with Nan. Ca2+-activated myosin ATPase activity was increased 35-39% in all fiber types in Nan animals. We conclude that, after Nan administration, the increase in Dia specific force results from the relatively greater Dia CSA occupied by hypertrophied muscle fibers, whereas the increased ATPase activity promotes a higher rate of cross-bridge turnover and thus increased Vo. We speculate that Nan in supraphysiological doses have the potential to offset or ameliorate conditions associated with enhanced proteolysis and disordered protein turnover. (+info)

Effects of implants on daily gains of steers wintered on dormant native tallgrass prairie, subsequent performance, and carcass characteristics. (2/470)

Fall-weaned crossbred steer calves (n = 300; 184 +/- 2.9 kg) received either no implant (Control) or were implanted with Synovex-C (SC = 10 mg estradiol benzoate + 100 mg progesterone), Synovex-S (SS = 20 mg estradiol benzoate + 200 mg progesterone), or Revalor-G (RG = 8 mg estradiol-17beta + 40 mg trenbolone acetate) to determine the effects of implants on weight gain during winter grazing on dormant tallgrass prairie, subsequent grazing and finishing performance, and carcass characteristics. Steers grazed two dormant tallgrass prairie pastures from October 16, 1996, until March 29, 1997 (164 d), and received 1.36 kg/d of a 25% CP supplement that supplied 100 mg of monensin/steer. Following winter grazing, all steers were implanted with Ralgro (36 mg zeranol) and grazed a common tallgrass prairie pasture until July 17 (110 d). After summer grazing, all steers were implanted with Revalor-S (24 mg estradiol-17beta + 120 mg trenbolone acetate), and winter implant treatment groups were equally allotted to four feedlot pens. Steers were harvested November 17, 1997, after a 123-d finishing period. Daily gains during the winter grazing phase averaged .28, .32, .32, or .35 kg/d, respectively, for Control, SC, SS, or RG steers and were greater (P < .01) for implanted steers than for Controls. Summer daily gains were similar (1.05 +/- .016 kg/d; P > or = .61) for all treatment groups. Feedlot daily gains were also similar (1.67 +/- .034 kg/d; P > or = .21), with implanted steers weighing 14 kg more than Control steers (P = .05) at harvest, despite similar management during summer grazing and feedlot phases. Control steers tended (P = .06) to have lower yield grades. There were no differences (P = .99) in marbling between implanted and nonimplanted steers. Steers implanted during the wintering phase had increased skeletal and overall (P < .01) carcass maturities compared with nonimplanted steers, which resulted in more "B" and "C" maturity carcasses. Because carcass maturity score affects quality grade, the increased maturities of implanted steers resulted in a $9.04 decrease in carcass value/100 kg (P < .01) compared with Controls. The results of this study indicate that growth-promoting implants are efficacious for cattle wintered on dormant native range despite low daily gains. This increased weight is maintained through the summer grazing and feedlot phases; however, the benefit of the increased weight may be offset by decreased carcass quality grade and value due to increased carcass maturity. (+info)

Increased dopaminergic and 5-hydroxytryptaminergic activities in male rat brain following long-term treatment with anabolic androgenic steroids. (3/470)

1. The effects of treating groups of rats with four different anabolic androgenic steroids (AAS) (testosterone, nandrolone, methandrostenolone, and oxymetholone) on 5-hydroxytryptamine (5-HT) and dopamine (DA) neurones in different brain regions were examined. The AAS was injected six times with 1 week's interval and the rats were sacrificed 2 days after the final injection. 5-HT and its metabolite 5-hydroxyindoleacetic acid (5-HIAA), DA and its metabolites 3,4-dihydroxyphenylacetic acid (DOPAC) and homovanillic acid (HVA) were measured. The effect on DA and 5-HT synthesis rate was analysed as the accumulation of 3,4-dihydroxyphenyl-alanine (DOPA) and 5-hydroxytryptophan (5-HTP), respectively, after inhibition of the amino acid decarboxylase with NSD-1015 (3-hydroxy-benzylhydrazine dihydrochloride). Additionally, the monoamine oxidase (MAO) activity was analysed in the hypothalamus. 2. The DOPAC + HVA/DA ratio was increased in the striatum in all treatment groups. However, the synthesis rate of DA was significantly increased only in the methandrostenolone treated group. 3. The 5-HIAA/5-HT ratio was increased in all treatment groups in the hippocampus, in the frontal cortex in the methandrostenolone-treated animals and in the hypothalamus in the testosterone- and oxymetholone-treated rats, while the 5-HT synthesis rate was not affected by the AAS-treatments. 4. The MAO-A activity was increased in the oxymetholone-treated rats while the other treatment groups were unaffected. The MAO-B activity was not changed. 5. The results indicate that relatively high doses of AAS increase dopaminergic and 5-hydroxytryptaminergic metabolism in male rat brain, probably due to enhanced turnover in these monaminergic systems. (+info)

Reversal of weightlessness-induced musculoskeletal losses with androgens: quantification by MRI. (4/470)

Microgravity causes rapid decrement in musculoskeletal mass is associated with a marked decrease in circulatory testosterone levels, as we reported in hindlimb-suspended (HLS) rats. In this model which simulates microgravity, we hypothesized that testosterone supplementation should prevent these losses, and we tested this in two studies. Muscle volumes and bone masses were quantitated by using magnetic resonance imaging (MRI) on day 12. In the first study, 12-wk-old Sprague-Dawley rats that were HLS for 12 days lost 28.5% of muscle volume (53.3 +/- 4.8 vs. 74.5 +/- 3.6 cm3 in the ground control rats; P < 0.001) and had a 5% decrease in bone mineral density (BMD) (P < 0.05). In the second study, 30 male 12-wk-old Wistar rats were HLS and were administered either a vehicle (control), testosterone, or nandrolone decanoate (ND). An additional 20 rats were used as ground controls, one-half of which received testosterone. HLS rats had a significant reduction in muscle volume (42.9 +/- 3.0 vs. 56 +/- 1.8 cm3 in ground control rats; P < 0.01). Both testosterone and ND treatments prevented this muscle loss (51.5 +/- 2 and 51.6 +/- 1.2 cm3, respectively; a 63% improvement; P < 0. 05). There were no statistical differences between the two active treatment groups nor with the ground controls. Similarly, there was an 85% improvement in BMD in the testosterone group (1.15 +/- 0.04 vs. 1.04 +/- 0.04 density units in vehicle controls; P < 0.05) and a 76% improvement in the ND group (1.13 +/- 0.07 density units), whereas ground control rats had a BMD of 1.17 +/- 0.03 density units. Because serum testosterone levels are markedly reduced in this model of simulated microgravity, androgen replacement seems to be a rational countermeasure to prevent microgravity-induced musculoskeletal losses. (+info)

Effects of anabolic-androgenic steroid use or gonadal testosterone suppression on serum leptin concentration in men. (5/470)

OBJECTIVE: Serum leptin concentration shows a sexual dimorphism that is not accounted for by gender differences in adiposity. A strong inverse association exists between serum leptin and testosterone concentrations in men, pointing to a likely influence of gonadal sex steroids on serum leptin concentration. The aim of this study was to investigate whether manipulation of sex steroid hormones in men would alter serum leptin concentration independently of changes in fat mass. DESIGN AND METHODS: The effects of sex steroid suppression on serum leptin concentration were investigated in nine healthy men in whom testosterone had been reversibly suppressed for 5 weeks after treatment with intramuscular triptorelin. The effects of sex steroid supplementation were investigated in nine male bodybuilders who self-administered anabolic--androgenic steroids (AAS) for a mean period of 6.5 weeks. A control group received no hormonal treatment. RESULTS: Testosterone concentration was significantly reduced by triptorelin administration (7.32+/- 1.92ng/ml at baseline compared with 1.15+/-0.57ng/ml at 5 weeks, P=0.002). High-dose AAS use was confirmed by urine analysis. Body fat percentage was unaffected by the AAS or triptorelin intervention (P>0.19). Leptin concentration was significantly reduced after one cycle of AAS use (2.40+/-0. 98ng/ml off cycle compared with 1.63+/-0.37ng/ml on cycle, P=0.012), and was significantly increased by triptorelin administration (2. 96+/-1.50ng/ml at baseline compared with 6.63+/-4.67ng/ml at five weeks, P=0.004). No significant change occurred in the control group. CONCLUSION: Androgenic sex hormone supplementation decreases serum leptin concentration, whereas suppression increases serum leptin concentration, independently of changes in body fat mass in healthy men. The sexual dimorphism evident in serum leptin concentration is likely to be due to a suppressive effect of testosterone on serum leptin concentration in males. (+info)

Effects of anabolic steroids on diaphragm impairment induced by methylprednisolone in emphysematous hamsters. (6/470)

This study was designed to investigate whether the administration of the anabolic steroid nandrolone decanoate is able to antagonize the loss in diaphragm function induced by long-term administration of a low-dose of methylprednisolone in emphysematous hamsters. Normal and emphysematous male hamsters were randomized to receive either saline or methylprednisolone 0.2 mg x kg(-1) x day(-1) for 9 months, with or without nandrolone decanoate 1 mg x kg(-1) x week(-1) i.m. during the final 3 months. Diaphragm contractile properties and myosin heavy chain composition were determined. Compared to control hamsters, the force generating capacity of isolated diaphragm strips decreased by approximately 12% in the emphysema group and by approximately 22% in the emphysema plus methylprednisolone group. Addition of nandrolone decanoate to the emphysema plus methylprednisolone hamsters significantly improved force generation. The atrophy of type IIa and IIx diaphragm fibres in the emphysema plus methylprednisolone group was completely reversed to the level of control hamsters by the addition of nandrolone decanoate. In conclusion, nandrolone decanoate in part reversed the loss in diaphragm force-generating capacity in emphysematous hamsters treated with methylprednisolone, and reversed type IIa and IIx fibre atrophy completely. (+info)

Effects of anabolic steroid (19-nortestosterone) on the secretion of testicular hormones in the stallion. (7/470)

The aim of this study was to clarify the effect of anabolic steroids on the testicular endocrine function of mature stallions. Mature thoroughbred stallions were treated with 800 mg nandrolone decanoate every 3 weeks for 3 months. After the first treatment, plasma concentrations of LH, immunoreactive inhibin and testosterone decreased rapidly to the nadir. These hormones were maintained at significantly lower concentrations compared with concentrations in intact stallions. Histology of the testicular tissue indicated the arrest of advanced spermatogenesis in the seminiferous tubules and a severe depletion of the number of Leydig cells in the interstitial compartment as a result of treatment. Most of the immunopositive cells for the inhibin alpha-subunit and steroidogenesis enzymes in the interstitial compartment decreased below detectable amounts, whereas immunopositive reactions of inhibin alpha-subunit in the seminiferous tubules were clearly observed. In conclusion, the treatment of mature stallions with nandrolone decanoate caused a decrease in the secretion of ir-inhibin and testosterone from the testis, the depletion of the number of Leydig cells and a decrease below detectable amounts of inhibin alpha-subunit and steroidogenesis enzymes. The concentration of ir-inhibin in the peripheral blood may be a useful marker for the examination of testicular activity in stallions being treated with anabolic steroids. (+info)

Over-the-counter anabolic steroids 4-androsten-3,17-dione; 4-androsten-3beta,17beta-diol; and 19-nor-4-androsten-3,17-dione: excretion studies in men. (8/470)

Since the appearance of 4-androsten-3,17-dione (I) as a nutritional supplement in early 1997, we have frequently observed a characteristic deterioration of endogenous steroid profiles in athletes' urine in routine anabolic steroid testing in which concentrations of major endogenous urinary steroids and testosterone exceed normal. Human excretion studies are performed with I and newer, over-the-counter "supplements" 4-androsten-3beta,17beta-diol (II) and 19-nor-4-androsten-3,17-dione (III). Endogenous urinary steroids affected by I and II are androsterone, etiocholanolone, their hydroxylated derivatives 5alpha- and 5beta-androstan-3alpha,17beta-diols, testosterone, and epitestosterone. Their concentrations briefly increase by one to two orders of magnitude and return to normal 24 h after oral administration of I and II. The average male may test positive for testosterone because testosterone concentration rises faster than that of epitestosterone, causing the testosterone/epitestosterone (T/E) ratio to rise above the positive cutoff of 6:1. A remarkable distinction in excretion patterns was observed in eastern Asian men, for whom I and II did not affect urinary concentrations of testosterone and did not increase the T/E ratio. First-pass metabolism deactivates most of the orally administered drugs I and II, rapidly converting them into inactive androsterone and etiocholanolone. Drug II is a more effective testosterone booster because of its different metabolic pathway. After the use of III, a precursor of the potent anabolic nandrolone, high concentrations of norandrosterone and noretiocholanolone appear in urine, similar to nandrolone. These are detectable in urine for 7-10 days after a single oral dose of III (50 mg). (+info)

... anabolic agents; diuretics and other masking agents; "street drugs" (the NCAA gives as examples heroin, marijuana, ...

https://en.wikipedia.org/wiki/NCAA_drug_testing

Anabolic Agents , List of Prohibited Substances and Methods". English. Archived from the original on May 27, 2016. Retrieved ... Testosterone is classified as an anabolic agent and is on the World Anti-Doping Agency (WADA) List of Prohibited Substances and ... and this is primarily responsible for the dissociation of anabolic and androgenic effects with these agents. In addition to DHT ... Taylor WN (2002). Anabolic Steroids and the Athlete (2nd ed.). McFarland. p. 180. ISBN 978-0-7864-1128-3. Archived from the ...

https://en.wikipedia.org/wiki/Testosterone_(medication)

von Deutsch DA, Abukhalaf IK, Lapu-Bula R (2003). "Anabolic Doping Agents". In Mozayani A, Raymon L (eds.). Handbook of Drug ... DHT has been reported to be a very poor anabolic agent when administered exogenously as a medication. In addition to normal ... Llewellyn W (2009). Anabolics. Molecular Nutrition Llc. pp. 19, 163. ISBN 978-0967930473. Chang C (2002). Androgens and ... 12-. ISBN 978-1-4832-6504-9. Taylor WN (2002). Anabolic Steroids and the Athlete (2d ed.). McFarland. pp. 178-. ISBN 978-0-7864 ...

https://en.wikipedia.org/wiki/Dihydrotestosterone

However, androstanolone is nonetheless described as a very poor anabolic agent. This is attributed to its high affinity as a ... von Deutsch DA, Abukhalaf IK, Lapu-Bula R (15 October 2003). "Anabolic Doping Agents". In Mozayani A, Raymon L (eds.). Handbook ... Llewellyn W (2011). Anabolics. Molecular Nutrition Llc. pp. 8, 23-25, 353-359. ISBN 978-0-9828280-1-4. Coutts SB, Kicman AT, ... The medication is a naturally occurring androgen and anabolic steroid and hence is an agonist of the androgen receptor (AR), ...

https://en.wikipedia.org/wiki/Androstanolone

Parr MK, Botrè F, Naß A, Hengevoss J, Diel P, Wolber G (June 2015). "Ecdysteroids: A novel class of anabolic agents?". Biology ... It has been found to increase hypertrophy in rats at a similar level to some anabolic androgenic steroids and SARM S 1. This is ... Phytoecdysteroids also appear in many plants mostly as a protection agents (toxins or antifeedants) against herbivore insects. ...

https://en.wikipedia.org/wiki/Ecdysteroid

... assays to determine methasterone's anabolic and androgenic activity were published in Vida's Androgens and Anabolic Agents, a ... Androgens and Anabolic Agents: Chemistry and Pharmacology. New York: Academic Press. pp. 23 & 168. Amy Shipley (November 30, ... "potent orally active anabolic agent exhibiting only weak androgenic activity." The results of subsequent ... as anabolic and 20% as androgenic, yielding a Q-ratio (anabolic to androgenic ratio) of 20, which is considered very high. It ...

https://en.wikipedia.org/wiki/Methasterone

She tested positive for Dehydrochlormethyltestosterone (S1.1 Anabolic agents). In November 2016, she was stripped of her 2012 ...

https://en.wikipedia.org/wiki/Cristina_Iovu

It is an anabolic (i.e., bone growing) agent. In 2017, it was approved to treat postmenopausal osteoporosis in the United ... It works as an anabolic agent for the bone, through selective activation of the parathyroid hormone 1 receptor (PTH1R), a G ... The anabolic effects of abaloparatide on bone were demonstrated in two preclinical studies conducted in ovariectomized rats. ... "FDA Approves Radius Health's TYMLOS (abaloparatide), a Bone Building Agent for the Treatment of Postmenopausal Women with ...

https://en.wikipedia.org/wiki/Abaloparatide

Metzler M (April 1989). "Metabolism of some anabolic agents: toxicological and analytical aspects". J. Chromatogr. 489 (1): 11- ... Trendione is listed in the United States Designer Anabolic Steroid Control Act of 2014. List of androgens/anabolic steroids ... A potent anabolic steroid with reduced androgenic and estrogenic activity". Steroids. 75 (6): 377-89. doi:10.1016/j.steroids. ... exhibits tissue selective anabolic activity: effects on muscle, bone, adiposity, hemoglobin, and prostate". Am. J. Physiol. ...

https://en.wikipedia.org/wiki/Trendione

... anabolic steroids, alcohol, opioids, efavirenz, alkylating agents, and omeprazole. Certain components of personal skin care ... Androgens/anabolic steroids may be effective for gynecomastia. Testosterone itself may not be suitable to treat gynecomastia as ... The use of anabolic steroids and exposure to chemicals that mimic estrogen in cosmetic products, organochlorine pesticides, and ... Potential sources of estrogen include oral contraceptive pills, spironolactone, and anabolic steroids. High levels of prolactin ...

https://en.wikipedia.org/wiki/Gynecomastia

Poole KE, Reeve J (Dec 2005). "Parathyroid hormone - a bone anabolic and catabolic agent". Current Opinion in Pharmacology. 5 ( ... Martin TJ (Mar 2004). "Does bone reabsorption inhibition affect the anabolic response to parathyroid hormone?". Trends in ...

https://en.wikipedia.org/wiki/Parathyroid_hormone

Poole KE, Reeve J (December 2005). "Parathyroid hormone - a bone anabolic and catabolic agent". Current Opinion in Pharmacology ...

https://en.wikipedia.org/wiki/Inorganic_pyrophosphatase

Anabolic agents: include the use of anabolic steroids that increase testosterone levels in players. The drug is prohibited as ... A full list of itemised anabolic agents is listed on the ITF website. Peptide hormones: include the use of drugs with amino ... Due to the change on hormones, the use of these agents can also effect athletes metabolism. Diuretics and masking agents: ... These substances can also dilute certain doping agents in the urine, and so are used by athletes to pass drug tests. In ...

https://en.wikipedia.org/wiki/Doping_in_tennis

The IOC said both samples indicated the presence of the anabolic agent metenolone. New Zealand's Valerie Adams was subsequently ...

https://en.wikipedia.org/wiki/Nadzeya_Astapchuk

Anabolic agents, or Anabolic Androgenic Steroids (AAS), are any of a group of synthetic or natural steroid hormones that builds ... Anabolic agents are abused by athletes in training to increase the size and strength of their muscles. However, the muscle ... Side effects with anabolic agents are very serious and are not to be ignored. Side effects include: acne, nervous tension, ... Examples of anabolic agents are boldenone, clenbuterol, dehydrocholormethyl-testosterone (DHEA), nandrolone, stanozolol, ...

https://en.wikipedia.org/wiki/NCAA_banned_substances

NADPH is used as a reducing agent in many anabolic reactions. Proton translocating NAD(P)+ transhydrogenase is one of the main ...

https://en.wikipedia.org/wiki/Proton-Translocating_NAD(P) _Transhydrogenase

For diuretic or masking agent-two regular and/or postseason games. For stimulants or anabolic agent-four regular and/or ... At the conclusion of the survey, researchers found that out of 2552 ex-NFL players, 9.1% self reported using anabolic steroids ... For a prohibited substance plus a diuretic or masking agent/attempt to substitute, dilute or adulterate a specimen/attempt to ... In the U.S., anabolic steroids are currently listed as Schedule III controlled substances under the Controlled Substances Act, ...

https://en.wikipedia.org/wiki/Doping_in_the_United_States

Anabolic agents may have some efficacy but are not often used due to side effects. There are multiple treatments and ...

https://en.wikipedia.org/wiki/Muscle_atrophy

The compound is listed as a banned anabolic agent by the World Anti-Doping Agency. Chlorodehydromethylandrostenediol ... orally active anabolic-androgenic steroid (AAS) and designer steroid that has been sold on the Internet as a "dietary ... Androgens and anabolic steroids, Androstanes, Designer drugs, Organochlorides, World Anti-Doping Agency prohibited substances) ...

https://en.wikipedia.org/wiki/Methylclostebol

On February 11, 2020, news surfaced that Prazeres tested positive for anabolic agents in two out-of-competition samples on ... "Michel Prazeres accepts two-year USADA sanction after testing positive for anabolic agent". mmafighting.com. Staff (2021-04-02 ...

https://en.wikipedia.org/wiki/Michel_Prazeres

July 2019). "Ecdysteroids as non-conventional anabolic agent: performance enhancement by ecdysterone supplementation in humans ... July 2019). "Ecdysteroids as non-conventional anabolic agent: performance enhancement by ecdysterone supplementation in humans ... The study was funded by the World Anti-Doping Agency (WADA) and demonstrated a significant dose-responsive anabolic effect of ... However, a number of earlier studies (,) supported the anabolic effects of 20-Hydroxyecdysone. A more recent study conducted in ...

https://en.wikipedia.org/wiki/20-Hydroxyecdysone

The most everyday use of prohormones is as supplements for muscle growth via ergogenic and anabolic agents. Prohormone ... used as ergogenic or anabolic agents for muscle growth. A commonly consumed example of said precursors are androstenedione and ... Anabolic Steroid Control Act of 2004. Many prohormone supplements that were claimed to impart anabolic or ergogenic effects in ... Pitts, Joseph R. (2014-12-18). "Text - H.R.4771 - 113th Congress (2013-2014): Designer Anabolic Steroid Control Act of 2014". ...

https://en.wikipedia.org/wiki/Prohormone

The World Anti-Doping Agency lists 7-keto-DHEA as a prohibited anabolic agent. The FDA has proposed that it be banned from use ... 7-Keto-DHEA is reported to be an anabolic androgenic steroid that may be subject to abuse in sport. "The World Anti-Doping Code ...

https://en.wikipedia.org/wiki/7-Keto-DHEA

He claims it was in an anti-baldness treatment; however, the drug is banned as it is a masking agent for anabolic steroids. On ...

https://en.wikipedia.org/wiki/Romário

... particularly anabolic agents such as steroids, are used in some countries to accelerate muscle growth in animals.: 33 This ... "Meet The Former Livestock Agent Who Started An International Vegan Food Business". Forbes.com. Archived from the original on ...

https://en.wikipedia.org/wiki/Meat

However, they have not generally been used for this purpose, and have instead mostly been used only as anabolic agents. In any ... This is in part due to the high ratio of anabolic to androgenic effect of nandrolone and its weak propensity for androgenic and ... As such, it is an androgen and anabolic steroid, or an agonist of the AR, the biological target of androgens like testosterone ... Along with oxandrolone (which has a ratio of about 10:1), nandrolone esters are thought to have the highest ratio of anabolic ...

https://en.wikipedia.org/wiki/Nandrolone_decanoate

The World Anti-Doping Agency is listing it as S1 Anabolic agent substance "prohibited at all times". In general, androgens such ... List of androgens/anabolic steroids List of human hormones Haynes WM, ed. (2011). CRC Handbook of Chemistry and Physics (92nd ... Testosterone is the primary sex hormone and anabolic steroid in males. In humans, testosterone plays a key role in the ... The Annual NY Academy of Sciences has also found anabolic steroid use (which increases testosterone) to be higher in teenagers ...

https://en.wikipedia.org/wiki/Testosterone

The substance was probenecid, a medicine for the kidney and also a masking agent for anabolic steroids. In 1988, every sport ... Delgado tested positive for the known masking agent Probenecid during the 1988 tour. The drug, which had been placed on the ...

https://en.wikipedia.org/wiki/Pedro_Delgado

Zhou tested positive to clenbuterol, a Class 1 Anabolic Agent on the WADA Prohibited List of substances. On 27 October 2011, ...

https://en.wikipedia.org/wiki/Zhou_Mi_(badminton)

... clenbuterol and other β2 adrenergic agents remain banned not as a beta-agonist, but rather an anabolic agent. These effects are ... Consequently, such agents are monitored for and generally banned by WADA (World Anti-Doping Agency) with limited permissible ... The comprehensive anabolic, lipolytic, and ergogenic effects of long-acting β2 agonists such as clenbuterol render them ... Choo JJ, Horan MA, Little RA, Rothwell NJ (July 1992). "Anabolic effects of clenbuterol on skeletal muscle are mediated by beta ...

https://en.wikipedia.org/wiki/Beta-2_adrenergic_receptor

ISBN 978-94-011-4439-1. Krüskemper HL (22 October 2013). Anabolic Steroids. Elsevier. pp. 200-. ISBN 978-1-4832-6504-9. Kern W ... ISBN 978-3-88763-075-1. Morton IK, Hall JM (6 December 2012). Concise Dictionary of Pharmacological Agents: Properties and ... is a synthetic androgen and anabolic steroid and a nandrolone ester that is or has been marketed in Italy. List of androgen ... Androgens and anabolic steroids, Nandrolone esters, Progestogens, Succinate esters, All stub articles, Genito-urinary system ...

https://en.wikipedia.org/wiki/Nandrolone_hydrogen_succinate

There have been experiments using a SARMs C-6 and S-23 on male mice as a contraceptive agent. Treatment of osteoporosis has ... A common, negative effect of SARMs and other anabolic steroids is the reduction of HDL and LDL, this has been confirmed in ... The potency of a SARM can be thought of as its potential anabolic activity in relation to its androgenic activity, VK5211 has ... They are intended to have the same kind of effects as androgenic drugs, such as anabolic-androgenic steroids, but be more ...

https://en.wikipedia.org/wiki/Selective_androgen_receptor_modulator

... told federal agents investigating steroids in baseball named Tejada as a user of "anabolic steroids." The Times reported that ... The A's elected not to re-sign the free agent, citing budget concerns and a young Bobby Crosby coming through the system, so ...

https://en.wikipedia.org/wiki/Miguel_Tejada

ISBN 978-3-88763-075-1. Morton IK, Hall JM (6 December 2012). Concise Dictionary of Pharmacological Agents: Properties and ... Androgens and anabolic steroids, Androstanes, Carbonate esters, Testosterone esters, All stub articles, Genito-urinary system ... is an androgen and anabolic steroid and a testosterone ester. Elks J (14 November 2014). The Dictionary of Drugs: Chemical Data ...

https://en.wikipedia.org/wiki/Testosterone_hexahydrobenzylcarbonate

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