Peptides, SARMs, & Prohormones: Where it Starts

GHRP (growth hormone releasing peptide)
GHRP 2, 6
ACVR2B (Ace-031)
BPC 157

Ligandrol (LGD-4033)
Ipamorelin MK677

Superdrol (Methasterone)
1AD (1-Androstenediol)
Laxogenin 100


Oxandrolone, sold under the brand names Oxandrin and Anavar, among others, is an androgen and anabolic steroid (AAS) medication which is used to help promote weight gain in various situations, to help offset protein catabolism caused by long-term corticosteroid therapy, to support recovery from severe burns, to treat bone pain associated with osteoporosis, to aid in the development of girls with Turner syndrome, and for other indications.[4][5][6] It is taken by mouth.[4]

DHT Derivative

Highly anabolic – Low Androgenic/Progesteronic effects
Doesn’t aromatize

FDA-approved for treating bone pain associated with osteoporosis, aiding weight gain following surgery or physical trauma, during chronic infection, or in the context of unexplained weight loss, and counteracting the catabolic effect of long-term corticosteroid therapy.[14][15

Not metabolized in the liver, mainly metabolized in the kidney, minimal liver toxicity

Men’s testosterone levels largely determined by where they grow up

Men who grow up in more challenging conditions where there is potential of exposure to infectious diseases, for example, are likely to have lower testosterone levels in later life than those who spend their childhood in healthier environments, according to new research.

Men’s testosterone levels are largely determined by their environment during childhood, according to new research.

The Durham University-led study suggests that men who grow up in more challenging conditions where there are lots of infectious diseases, for example, are likely to have lower testosterone levels in later life than those who spend their childhood in healthier environments.

The study, published in Nature Ecology and Evolution, challenges the theory that testosterone levels are controlled by genetics or race.

As high testosterone levels potentially lead to an increased risk of prostate enlargement and cancer, the researchers suggest that any screening for risk profiles may need to take a man’s childhood environment into account.

The study found that Bangladeshi men who grew up and lived as adults in the UK had significantly higher levels of testosterone compared to relatively well-off men who grew up and lived in Bangladesh as adults. Bangladeshis in Britain also reached puberty at a younger age and were taller than men who lived in Bangladesh throughout their childhood.

The researchers say the differences are linked to energy investment as it may only be possible to have high testosterone levels if there are not many other demands placed on the body such as fighting off infections.?In environments where people are more exposed to disease or poor nutrition, developing males direct energy towards survival at the cost of testosterone.

The researchers collected data from 359 men on height, weight, age of puberty and other health information along with saliva samples to examine their testosterone levels. They compared the following groups: men born and still resident in Bangladesh; Bangladeshi men who moved to the UK (London) as children; Bangladeshi men who moved to the UK as adults; second-generation, UK-born men whose parents were Bangladeshi migrants; and UK-born ethnic Europeans.

Lead author of the study, Dr Kesson Magid from Durham University’s Department of Anthropology (UK), said: “A man’s absolute levels of testosterone are unlikely to relate to their ethnicity or where they live as adults but instead reflect their surroundings when they were children.”

Men with higher levels of testosterone are at greater risk of potentially adverse effects of this hormone on health and ageing. Very high levels can mean increased muscle mass, increased risk of prostate diseases and have been linked to higher aggression. Very low testosterone levels in men can include lack of energy, loss of libido and erectile dysfunction. The testosterone levels of the men in the study were, however, all in a range that would unlikely have an impact on their fertility.

Co-author Professor Gillian Bentley from Durham University, commented: “Very high and very low testosterone levels can have implications for men’s health and it could be important to know more about men’s childhood circumstances to build a fuller picture of their risk factors for certain conditions or diseases.”

Aspects of male reproductive function remain changeable into adolescence, up to the age of 19 and are more flexible in early rather than late childhood, according to the research. However, the study suggests that, in adulthood, men’s testosterone levels are no longer heavily influenced by their surroundings.

Senior co-author Gillian Bentley and colleagues have also previously found that the environment in which girls grow up can affect their hormone levels, fertility and risk levels for reproductive cancers as adults.

The research was funded by the Economic and Social Research Council (ESRC), the Royal Society and Prostate Cancer UK, and involved researchers from the University of Chittagong (Bangladesh), Durham University (UK), and Northwestern University (USA).

Story Source

Materials provided by Durham UniversityNote: Content may be edited for style and length.


  1. Kesson Magid, Robert T. Chatterton, Farid Uddin Ahamed, Gillian R. Bentley. Childhood ecology influences salivary testosterone, pubertal age and stature of Bangladeshi UK migrant menNature Ecology & Evolution, 2018; DOI: 10.1038/s41559-018-0567-6

Testosterone dose-response in healthy young men



Testosterone increases muscle mass and strength and regulates other physiological processes, but we do not know whether testosterone effects are dose dependent and whether dose requirements for maintaining various androgen-dependent processes are similar. To determine the effects of graded doses of testosterone on body composition, muscle size, strength, power, sexual and cognitive functions, prostate-specific antigen (PSA), plasma lipids, hemoglobin, and insulin-like growth factor I (IGF-I) levels, 61 eugonadal men, 18–35 yr, were randomized to one of five groups to receive monthly injections of a long-acting gonadotropin-releasing hormone (GnRH) agonist, to suppress endogenous testosterone secretion, and weekly injections of 25, 50, 125, 300, or 600 mg of testosterone enanthate for 20 wk.

Energy and protein intakes were standardized. The administration of the GnRH agonist plus graded doses of testosterone resulted in mean nadir testosterone concentrations of 253, 306, 542, 1,345, and 2,370 ng/dl at the 25-, 50-, 125-, 300-, and 600-mg doses, respectively. Fat-free mass increased dose dependently in men receiving 125, 300, or 600 mg of testosterone weekly (change +3.4, 5.2, and 7.9 kg, respectively). The changes in fat-free mass were highly dependent on testosterone dose (P = 0.0001) and correlated with log testosterone concentrations (r = 0.73, P = 0.0001). Changes in leg press strength, leg power, thigh and quadriceps muscle volumes, hemoglobin, and IGF-I were positively correlated with testosterone concentrations, whereas changes in fat mass and plasma high-density lipoprotein (HDL) cholesterol were negatively correlated. Sexual function, visual-spatial cognition and mood, and PSA levels did not change significantly at any dose.

We conclude that changes in circulating testosterone concentrations, induced by GnRH agonist and testosterone administration, are associated with testosterone dose- and concentration-dependent changes in fat-free mass, muscle size, strength and power, fat mass, hemoglobin, HDL cholesterol, and IGF-I levels, in conformity with a single linear dose-response relationship. However, different androgen-dependent processes have different testosterone dose-response relationships.

Testosterone regulates many physiological processes, including muscle protein metabolism, some aspects of sexual and cognitive functions, secondary sex characteristics, erythropoiesis, plasma lipids, and bone metabolism. However, testosterone dose dependency of various androgen-dependent processes is not well understood. Administration of replacement doses of testosterone to hypogonadal men and of supraphysiological doses to eugonadal men increases fat-free mass, muscle size, and strength.

Conversely, suppression of endogenous testosterone concentrations is associated with loss of fat-free mass and a decrease in fractional muscle protein synthesis. However, not known are whether testosterone effects on the muscle are dose dependent, or the nature of the testosterone dose-response relationships. Androgen receptors in most tissues are either saturated or downregulated at physiological testosterone concentrations; this leads to speculation that there might be two separate dose-response curves: one in hypogonadal range, with maximal response at low normal testosterone concentrations, and a second in supraphysiological range, representing a separate mechanism of action. However, testosterone dose-response relationships for a range of androgen-dependent functions in humans have not been studied.

Animal studies suggest that different androgen-dependent processes have different androgen dose-response relationships. Sexual function in male mammals is maintained at serum testosterone concentrations that are at the lower end of the male range. However, it is not known whether the low normal testosterone levels that normalize sexual function are sufficient to maintain muscle mass and strength, or whether the higher testosterone concentrations required to maintain muscle mass and strength might adversely affect plasma lipids, hemoglobin levels, and the prostate.

This information is important for optimizing testosterone replacement regimens for treatment of hypogonadal men. Also, for the proposed use of testosterone in sarcopenia associated with ageing and chronic illness, it is important to know whether significant gains in muscle mass and strength can be achieved at testosterone doses that do not adversely affect plasma high-density lipoprotein (HDL) and prostate-specific antigen (PSA) levels.

Therefore, the primary objective of this study was to determine the dose dependency of testosterone’s effects on fat-free mass and muscle performance. We hypothesized that changes in circulating testosterone concentrations would be associated with dose-dependent changes in fat-free mass, muscle strength, and power in conformity with a single linear dose-response relationship and that the dose requirements for maintaining other androgen-dependent processes would be different.

We treated young men with a long-acting gonadotropin-releasing hormone (GnRH) agonist to suppress endogenous testosterone secretion, and concomitantly also with one of five testosterone-dose regimens to create different levels of serum testosterone concentrations extending from subphysiological to the supraphysiological range. The lowest testosterone dose, 25 mg weekly, was selected because this dose had been shown to maintain sexual function in GnRH antagonist-treated men. The selection of the 600-mg weekly dose was based on the consideration that this was the highest dose that had been safely administered to men in controlled studies.




This was a double-blind, randomized study consisting of a 4-wk control period, a 20-wk treatment period, and a 16-wk recovery period. Each participant provided informed consent, approved by the institutional review boards of Drew University and Harbor-UCLA Research and Education Institute.


The participants were healthy men, 18–35 yr of age, with prior weight-lifting experience and normal testosterone levels. These men had not used any anabolic agents and had not participated in competitive sports events in the preceding year, and they were not planning to participate in competitive events in the following year.


Sixty-one eligible men were randomly assigned to one of five groups. All received monthly injections of a long-acting GnRH agonist to suppress endogenous testosterone production. In addition, group 1 received 25 mg of testosterone enanthate intramuscularly weekly;group 2, 50 mg testosterone enanthate; group 3, 125 mg testosterone enanthate; group 4, 300 mg testosterone enanthate; and group 5, 600 mg testosterone enanthate. Twelve men were assigned to group 1, 12 to group 2, 12 to group 3, 12 to group 4, and 13 togroup 5. Testosterone and GnRH agonist injections were administered by the General Clinical Research Center staff to assure compliance.

Nutritional intake.

Energy and protein intakes were standardized at 36 kcal · kg−1 · day−1 and 1.2 g · kg−1 · day−1, respectively. The standardized diet was initiated 2 wk before treatment was started; dietary instructions were reinforced every 4 wk. The nutritional intake was verified by analysis of 3-day food records and 24-h food recalls every 4 wk by use of the Minnesota Nutritional Software.

Exercise stimulus.

The participants were asked not to undertake strength training or moderate-to-heavy endurance exercise during the study. These instructions were reinforced every 4 wk.

Outcome measures.

Body composition and muscle performance were assessed at baseline and during week 20. Fat-free mass and fat mass were measured by underwater weighing and dual-energy X-ray absorptiometry (DEXA, Hologic 4500, Waltham, MA). Total thigh muscle and quadriceps muscle volumes were measured by MRI scanning.

For estimation of total body water, the men ingested 10 g of2H2O, and plasma samples were drawn at −15, 0, 120, 180, and 240 min. We measured2H abundance in plasma by nuclear magnetic resonance spectroscopy, with a correction factor of 0.985 for exchangeable hydrogen. We measured bilateral leg press strength by use of the one-repetition maximum (1-RM) method. A seated leg press exercise with pneumatic resistance (Keiser Sport, Fresno, CA) was used for this purpose. Subjects performed 5–10 min of leg cycling and stretching warm-up and received instruction and practice in lifting mechanics before performing progressive warm-up lifts leading to the 1-RM. Seat position and the ensuing knee and hip angles, as well as foot placement, were measured and recorded for use in subsequent testing.

To ensure reliability in this highly effort-dependent test, the 1-RM score was reassessed within 7 days, but not sooner than 2 days, after the first evaluation. If duplicate scores were within 5%, the higher of the two values was accepted as the strength score. If the two tests differed by >5%, additional studies were conducted, ≥2 days apart but within 7 days, until the two highest scores were within 5%. No subject required >2 days of strength assessment.

We also measured leg power, because power in the lower extremity is strongly related to the performance of functional activities in the elderly. The sarcopenia that accompanies ageing is due in large part to a loss of the fast-twitch type II fibers and the coincident decrease in explosive force. Muscular power is important in performing such daily activities as rising from a chair, climbing stairs, and walking with speed. Leg power was measured with a previously validated Nottingham leg extensor power rig. Subjects performed 10–15 trials of the right leg and hip extension, attempting to generate as much force as possible by accelerating the leg rig’s weighted flywheel from rest.

The power score (in watts) was taken as the highest value observed during these trials with evidence of a plateau. As with the strength tests, power measurements were preceded by a 5- to 10-min warm-up, stretching, and practice. The power tests were repeated within 7 days, but not sooner than 2 days, after the first tests to reduce the effect of familiarization. To minimize test-retest variability, the angle of knee flexion and the seat position were recorded and maintained constant across tests.

Sexual function was assessed by daily logs of sexual activity and desire that were maintained for 7 consecutive days at baseline and during treatment by use of a published instrument. Spatial cognition was assessed by a computerized checkerboard test and mood by Hamilton’s depression and Young’s mania scales.

Adverse experiences, blood counts and chemistries, PSA, plasma lipids, total and free testosterone, luteinizing hormone (LH), sex steroid-binding globulin (SHBG), and insulin-like growth factor I (IGF-I) levels were measured periodically during control and treatment periods. Serum total testosterone was measured by an immunoassay; free testosterone by equilibrium dialysis; LH, SHBG, and PSA by immunoradiometric assays; and IGF-I by acid-ethanol extraction and immunoassay. The sensitivities and intra- and interassay coefficients of variation for hormone assays were as follows: total testosterone (0.6 ng/dl), 8.2 and 13.2%; free testosterone (0.22 pg/ml), 4.2 and 12.3%; LH (0.05 U/l), 10.7 and 13.0%; SHBG (6.25 nmol/l), 4 and 6%; PSA (0.01 ng/ml), 5.0 and 6.4%; and IGF-I (80 ng/ml), 4 and 6%, respectively. These assays have been validated previously.

Statistical analyses.

All variables were examined for their distribution characteristics. Variables not meeting the assumption of a normal distribution were log-transformed and retested. An ANOVA was used to compare change from baseline in outcome measures among the five groups. All outcome measures were analyzed using a paired t-test to detect a non-zero change from baseline within each group. P < 0.05 was considered statistically significant.

To describe the relationship between testosterone concentrations (T) and change in fat-free mass (Y) during testosterone administration, we tested three models: a linear model (Y = a +bT); a logarithmic model, Y = a +b · X, where X = log (T), and a and b represent the intercept and slope, respectively; and a growth model, Y = a/(1 +b · e−k · X). The logarithmic model provided the best fit for the data and was used to model the effects of testosterone concentrations on the change in other outcome variables. The correlations between testosterone concentrations and change in outcome variables are derived from this model. We also modelled the linear dependence of the change in outcome variables on testosterone dose by use of linear regression.




Participant characteristics.

Of 61 men enrolled, 54 completed the study: 12 in group 1, 8 in group 2, 11 in group 3, 10 in group 4, and 13 in group 5. One man discontinued treatment because of acne; other subjects were unable to meet the demands of the protocol. The five groups did not significantly differ with respect to their baseline characteristics (Table1).



All evaluable subjects received 100% of their GnRH agonist injections, and only one man in the 125-mg group missed one testosterone injection.

Nutritional intake.

Daily energy intake and proportion of calories derived from protein, carbohydrate, and fat were not significantly different among the five groups at baseline. There was no significant change in daily caloric, protein, carbohydrate, or fat intake in any group during treatment (data not shown).

Hormone levels.

Serum total and free testosterone levels (Table2), measured during week 16, 1 wk after the previous injection, were linearly dependent on the testosterone dose (P = 0.0001). Serum total and free testosterone concentrations decreased from baseline in men receiving the 25- and 50-mg doses and increased at 300- and 600-mg doses. Serum LH levels were suppressed in all groups. Serum SHBG levels decreased dose dependently at the 300- and 600-mg doses but did not change in other groups. Serum IGF-I concentrations increased dose dependently at the 300- and 600-mg doses (correlation between log testosterone level and change in IGF-I = 0.55, P = 0.0001). IGFBP-3 levels did not change significantly in any group.


Body composition.

Fat-free mass, measured by underwater weighing, did not change significantly in men receiving the 25- or 50-mg testosterone dose, but it increased dose dependently at higher doses (Table3). The changes in fat-free mass were highly dependent on testosterone dose (P = 0.0001) and correlated with log total testosterone concentrations during treatment (r = 0.73, P = 0.0001, see Fig. 2).


Changes in fat-free mass, measured by DEXA scan, were qualitatively similar to those obtained from underwater weighing (Table3, Fig. 1). The measurements of fat-free mass by DEXA were highly correlated with values obtained from underwater weighing (r = 0.94, P < 0.0001)


Fig. 1.

Change in fat-free mass (A), fat mass (B), leg press strength (C), thigh muscle volume (D), quadriceps muscle volume (E), sexual function (F), insulin-like growth factor I (G), and prostate-specific antigen (H). Data are means ± SE. *Significant differences from all other groups (P < 0.05); ❖significant difference from 25-, 50-, and 125-mg doses (P < 0.05); +significant difference from 25- and 50-mg doses (P < 0.05); and ✞significant difference from 25-mg dose (P < 0.05).

To determine whether the apparent changes in fat-free mass by DEXA scan and underwater weighing represented water retention, we measured total body water and compared the ratios of total body water to fat-free mass before and after treatment in each group. The ratios of total body water to fat-free mass by underwater weighing did not significantly change with treatment in any treatment group (Table 3), indicating that the apparent increase in fat-free mass measured by underwater weighing did not represent water retention in excess of that associated with protein accretion.

Fat mass, measured by underwater weighing, increased significantly in men receiving the 25- and 50-mg doses but did not change in men receiving the higher doses of testosterone (Table 3, Fig. 1). There was an inverse correlation between change in fat mass by underwater weighing and log testosterone concentrations (r = −0.60, P = 0.0001, Fig.2).


Fig. 2.

Relationship between serum testosterone concentrations (T) during treatment (week 16) and change in fat-free mass (A), fat mass (B), leg press strength (C), thigh muscle volume (D), quadriceps muscle volume (E), sexual function (F), insulin-like growth factor I (G), and prostate-specific antigen (H). The correlation coefficient, r, was calculated using the logarithmic model, Y = a +b · X, where X = log (T), and a and represent the intercept and slope.

Muscle size.

The thigh muscle volume and quadriceps muscle volume did not significantly change in men receiving the 25- or 50-mg doses but increased dose dependently at higher doses of testosterone (Table4, Fig. 1). The changes in thigh muscle and quadriceps muscle volumes correlated with log testosterone levels during treatment (r = 0.66, P = 0.0001, and r = 0.55, P = 0.0001, respectively, Fig. 2).


Muscle performance.

The leg press strength did not change significantly in the 25- and 125-mg-dose groups but increased significantly in those receiving the 50-, 300-, and 600-mg doses (Table 5). The changes in leg press strength correlated with log testosterone levels during treatment (r = 0.48, P = 0.0005, Fig. 2) and changes in muscle volume (r = 0.54,P = 0.003) and fat-free mass (r = 0.74,P < 0.0001).


Leg power, measured by the Nottingham leg rig, did not change significantly in men receiving the 25-, 50-, and 125-mg doses of testosterone weekly, but it increased significantly in those receiving the 300- and 600-mg doses. The increase in leg power correlated with log testosterone concentrations (r = 0.39,P = 0.0105, Fig. 2) and changes in fat-free mass (r = 0.30, P = 0.0392) and muscle strength (r = 0.42, P = 0.0020).

Behavioural measures.

The scores for sexual activity and sexual desire measured by daily logs did not change significantly at any dose. Similarly, visual-spatial cognition (Table 6) and mood, as assessed by Hamilton’s depression and Young’s manic scales (data not shown), did not change significantly in any group.


Adverse experiences and safety measures.

Hemoglobin levels decreased significantly in men receiving the 50-mg dose but increased at the 600-mg dose; the changes in hemoglobin were positively correlated with testosterone concentrations (r = 0.66, P = 0.0001) (Table7). Changes in plasma HDL cholesterol, in contrast, were negatively dependent on testosterone dose (P = 0.0049) and correlated with testosterone concentrations (r = −0.40, P = 0.0054). Total cholesterol, plasma low-density lipoprotein cholesterol, and triglyceride levels did not change significantly at any dose. Serum PSA, creatinine, bilirubin, alanine aminotransferase, and alkaline phosphatase did not change significantly in any group, but aspartate aminotransferase decreased significantly in the 25-mg group. Two men in the 25-mg group, five in the 50-mg group, three in the 125-mg group, seven in the 300-mg group, and two in the 600-mg group developed acne. One man receiving the 50-mg dose reported decreased ability to achieve erections.




GnRH agonist administration suppressed endogenous LH and testosterone secretion; therefore, circulating testosterone concentrations during treatment were proportional to the administered dose of testosterone enanthate. This strategy of combined administration of GnRH agonist and graded doses of testosterone enanthate was effective in establishing different levels of serum testosterone concentrations among the five treatment groups. The different levels of circulating testosterone concentrations created by this regimen were associated with dose- and concentration-dependent changes in fat-free mass, fat mass, thigh and quadriceps muscle volume, muscle strength, leg power, hemoglobin, circulating IGF-I, and plasma HDL cholesterol. Serum PSA levels, sexual desire and activity, and spatial cognition did not change significantly at any dose. The changes in fat-free mass, muscle volume, leg press strength and power, hemoglobin, and IGF-I were positively correlated, whereas changes in plasma HDL cholesterol and fat mass were negatively correlated with testosterone dose and total and free testosterone concentrations during treatment.

The compliance with the treatment regimen was high. The participants received 100% of their scheduled GnRH agonist and 99% of testosterone injections. Serum LH levels were suppressed in all men, demonstrating the effectiveness of GnRH agonist treatment. The treatment regimen was well tolerated. There were no significant changes in PSA or liver enzymes at any dose. However, long-term effects of androgen administration on the prostate, cardiovascular risk, and behaviour are unknown.

Serum testosterone levels were measured 7 days after the previous injection; they reflect the lowest testosterone levels after an injection. Testosterone concentrations were higher at other time points. Weekly injections of testosterone enanthate are associated with fluctuations in testosterone levels. Although nadir testosterone concentrations were highly correlated with testosterone enanthate dose, it is possible that sustained testosterone delivery by a patch or gel might reveal different dose-response relationships, particularly with respect to hemoglobin and HDL cholesterol.

There were no significant changes in overall sexual activity or sexual desire in any group, including those receiving the 25-mg dose. Testosterone replacement of hypogonadal men improves the frequency of sexual acts and fantasies, sexual desire, and response to visual erotic stimuli. Our data demonstrate that serum testosterone concentration at the lower end of the male range can maintain some aspects of sexual function. Testosterone has been shown to regulate nitric oxide synthase activity in the cavernosal smooth muscle, and it is possible that optimum penile rigidity might require higher testosterone levels than those produced by the 25-mg dose.

This study demonstrates that an increase in circulating testosterone concentrations results in dose-dependent increases in fat-free mass, muscle size, strength, and power. The relationships between circulating testosterone concentrations and changes in fat-free mass and muscle size conform to a single log-linear dose-response curve. Our data do not support the notion of two separate dose-response curves reflecting two independent mechanisms of testosterone action on the muscle. Forbes et al. predicted 25 years ago that the muscle mass accretion during androgen administration is related to the cumulative androgen dose, the product of daily dose and treatment duration. Our data are consistent with Forbes’s hypothesis of a linear relationship between testosterone dose and lean mass accretion; however, we do not know whether increasing the treatment duration would lead to further gains in muscle mass.

In addition, we do not know whether responsiveness to testosterone is attenuated in older men. Testosterone dose-response relationships might be modulated by other muscle growth regulators, such as nutritional status, exercise and activity level, glucocorticoids, thyroid hormones, and endogenous growth hormone secretory status.

Serum PSA levels decrease after androgen withdrawal, and testosterone replacement of hypogonadal men increases PSA levels into the normal range. We did not find significant changes in PSA at any dose, indicating that the lowest dose of testosterone maintained PSA levels. We did not measure prostate volume in this study; therefore, we do not know whether prostate volume exhibits the same relationship with testosterone dose as PSA levels.

Hemoglobin levels changed significantly in relation to testosterone dose and concentration. Testosterone regulates erythropoiesis through its effects on erythropoietin and stem cell proliferation (1. Although modest increments in hemoglobin might be beneficial in androgen-deficient men with chronic illness who are anemic, marked increases in hemoglobin levels could increase the risk of cerebrovascular events and hypertension.

Although men, on average, perform better on tests of spatial cognition than women, testosterone replacement has not been consistently shown to improve spatial cognition in hypogonadal men. We did not find changes in spatial cognition at any dose. The effect size of gender differences in spatial cognition is small; it is possible that our study did not have sufficient power to detect small differences. We cannot exclude the possibility that gender differences in spatial cognition might be due to organizational effects of testosterone and might not respond to changes in testosterone levels in adult men.

Although the mean change in fat-free mass and muscle size correlated with testosterone dose and concentration, there was considerable heterogeneity in response to testosterone administration within each group. These individual differences in response to androgen administration might reflect differences in activity level, testosterone metabolism, nutrition, or polymorphisms in androgen receptor, myostatin, 5-α-reductase, or other muscle growth regulators.

Our data demonstrate that different androgen-dependent processes have different testosterone dose-response relationships. Some aspects of sexual function and spatial cognition, and PSA levels, were maintained by relatively low doses of testosterone in GnRH agonist-treated men and did not increase further with administration of higher doses of testosterone. In contrast, graded doses of testosterone were associated with dose and testosterone concentration-dependent changes in fat-free mass, fat mass, muscle volume, leg press strength and power, hemoglobin, IGF-I, and plasma HDL cholesterol. The precise mechanisms for the tissue- and function-specific differences in testosterone dose dependence are not well understood. Although only a single androgen receptor protein is expressed in all androgen-responsive tissues, tissue specificity of androgen action might be mediated through combinatorial recruitment of tissue-specific coactivators and corepressors.

Testosterone doses associated with significant gains in fat-free mass, muscle size, and strength were associated with significant reductions in plasma HDL concentrations. Further studies are needed to determine whether clinically significant anabolic effects of testosterone can be achieved without adversely affecting cardiovascular risk. Selective androgen receptor modulators that preferentially augment muscle mass and strength, but only minimally affect prostate and cardiovascular risk factors, are desirable.

This study was supported primarily by National Institutes of Health (NIH) Grant 1RO1-AG-14369; additional support was provided by Grants 1RO1-DK-49296, 1RO1-DK-59297–01, Federal Drug Administration Grant ODP 1397, a General Clinical Research Center Grant MO-00425, NIH-National Center for Research Resources-00954, RCMI Grants P20-RR-11145–01 (RCMI Clinical Research Initiative) and G12-RR-03026. BioTechnology General (Iselin, NJ) provided testosterone enanthate, and R. P. Debio (Martigny, Switzerland) provided the GnRH agonist (Decapeptyl)





1. Alexander GM , Swerdloff RS , Wang C , Davidson T , McDonald V , Steiner B , Hines M. .Androgen-behavior correlations in hypogonadal men and eugonadal men. II. Cognitive abilities..Horm Behav 33: 85-94, 1998.
Crossref PubMed ISI Google Scholar

2. Antonio J , Wilson JD , George FW. .Effects of castration and androgen treatment on androgen-receptor levels in rat skeletal muscles..J Appl Physiol 87: 2016-2019, 1999.
Abstract ISI Google Scholar

3. Bagatell CJ , Heiman JR , Rivier JE , Bremner WJ. .Effects of endogenous testosterone and estradiol on sexual behavior in normal young men..J Clin Endocrinol Metab 78: 711-716, 1994.
PubMed ISI Google Scholar

4. Bassey EJ , Fiatarone MA , O’Neill EF , Kelly M , Evans WJ , Lipsitz LA. .Leg extensor power and functional performance in very old men and women..Clin Sci (Colch) 82: 321-327, 1992.
Crossref Google Scholar

5. Bassey EJ , Short AH. .A new method for measuring power output in a single leg extension: feasibility, reliability and validity..Eur J Appl Physiol 60: 385-390, 1990.
Crossref ISI Google Scholar

6. Bhasin S. .The dose-dependent effects of testosterone on sexual function and on muscle mass and function..Mayo Clin Proc 75, Suppl: S70-S75, 2000.
PubMed Google Scholar

7. Bhasin S , Bremner WJ. .Clinical review 85: emerging issues in androgen replacement therapy..J Clin Endocrinol Metab 82: 3-8, 1997.
PubMed ISI Google Scholar

8. Bhasin S , Fielder TJ , Peacock N , Sod-Moriah UA , Swerdloff RS. .Dissociating antifertility effects of GnRH-antagonist from its adverse effects on mating behavior in male rats..Am J Physiol Endocrinol Metab 254: E84-E91, 1988.
Link ISI Google Scholar

9. Bhasin S , Storer TW , Berman N , Callegari C , Clevenger B , Phillips J , Bunnell TJ , Tricker R , Shirazi A , Casaburi R. .The effects of supraphysiologic doses of testosterone on muscle size and strength in normal men..N Engl J Med335: 1-6, 1996.
Crossref PubMed ISI Google Scholar

10. Bhasin S , Storer TW , Berman N , Yarasheski KE , Cleveneger B , Casaburi RA. .A replacement dose of testosterone increases fat-free mass and muscle size in hypogonadal men..J Clin Endocrinol Metab 82: 407-413, 1997.
PubMed ISI Google Scholar

11. Bhasin S , Storer TW , Javanbakht M , Berman N , Yarasheski KE , Phillips J , Dike M , Sinha-Hikim I , Shen R , Hays RD , Beall G. .Testosterone replacement and resistance exercise in HIV-infected men with weight loss and low testosterone levels..JAMA 283: 763-770, 2000.
Crossref PubMed ISI Google Scholar

12. Brodsky IG , Balagopal P , Nair KS. .Effects of testosterone replacement on muscle mass and muscle protein synthesis in hypogonadal men—a clinical research center study..J Clin Endocrinol Metab 81: 3469-3475, 1996.
PubMed ISI Google Scholar

13. Buena F , Swerdloff RS , Steiner BS , Lutchmansingh P , Peterson MA , Pandian MR , Galmarini M , Bhasin S. .Sexual function does not change when serum testosterone levels are pharmacologically varied within the normal male range..Fertil Steril 59: 1118-1123, 1993.
Crossref PubMed ISI Google Scholar

14. Byron JW. .Effect of steroids on the cycling of haemopoietic stem cells..Nature 228: 1204-1206, 1970.
Crossref PubMed ISI Google Scholar

15. Carani C , Granata AR , Bancroft J , Marrama P. .The effects of testosterone replacement on nocturnal penile tumescence and rigidity and erectile response to visual erotic stimuli in hypogonadal men..Psychoneuroendocrinology 20: 743-753, 1995.
Crossref PubMed ISI Google Scholar

16 .Cooper CS , Perry PJ , Sparks AE , MacIndoe JH , Yates WR , Williams RD. .Effect of exogenous testosterone on prostate volume, serum and semen prostate specific antigen levels in healthy young men..J Urol 159: 441-443, 1998.
Crossref PubMed ISI Google Scholar

17. Cunningham GR , Hirshkowitz M , Korenman SG , Karacan I. .Testosterone replacement therapy and sleep-related erections in hypogonadal men..J Clin Endocrinol Metab 70: 792-797, 1990.
Crossref PubMed ISI Google Scholar

18. Dahlberg E , Snochowski M , Gustafsson J-A. .Regulation of androgen and glucocorticoid receptors in rat and mouse skeletal muscle cytosol..Endocrinology 108: 1431-1440, 1981.
Crossref PubMed ISI Google Scholar

19. Dobs AS , Meikle AW , Arver S , Sanders SW , Caramelli KE , Mazer NA. .Pharmacokinetics, efficacy, and safety of a permeation-enhanced testosterone transdermal system compared with bi-weekly injections of testosterone enanthate for the treatment of hypogonadal men..J Clin Endocrinol Metab 84: 3469-3478, 1999.
PubMed ISI Google Scholar

20. Faries D , Herrera J , Rayamajhi J , DeBrota D , Demitrack M , Potter WZ. .The responsiveness of the Hamilton Depression Rating Scale..J Psychiatr Res 34: 3-10, 2000.
Crossref PubMed ISI Google Scholar

21. Fielder TJ , Peacock NR , McGivern RF , Swerdloff RS , Bhasin S. .Testosterone dose-dependency of sexual and nonsexual behaviors in the gonadotropin-releasing hormone antagonist-treated male rat..J Androl 10: 167-173, 1989.
Crossref PubMed Google Scholar

22. Forbes GB. .The effect of anabolic steroids on lean body mass: the dose response curve..Metabolism 34: 571-573, 1985.
Crossref PubMed ISI Google Scholar

23. Forbes GB , Porta CR , Herr BE , Griggs RC. .Sequence of changes in body composition induced by testosterone and reversal of changes after drug is stopped..JAMA 267: 397-399, 1992.
Crossref PubMed ISI Google Scholar

24. Fristad MA , Weller RA , Weller EB. .The Mania Rating Scale (MRS): further reliability and validity studies with children..Ann Clin Psychiatry 7: 127-132, 1995.
Crossref PubMed Google Scholar

25. Gillum RF , Sempos CT. .Hemoglobin, hematocrit, and stroke incidence and mortality in women and men..Stroke 27: 1910-1914, 1996.
PubMed ISI Google Scholar

26. Griggs RC , Kingston W , Jozefowicz RF , Herr BE , Forbes G , Halliday D. .Effect of testosterone on muscle mass and muscle protein synthesis..J Appl Physiol 66: 498-503, 1989.
Link ISI Google Scholar

27. Grinspoon S , Corcoran C , Askari H , Schoenfeld D , Wolf L , Burrows B , Walsh M , Hayden D , Parlman K , Anderson E , Basgoz N , Klibanski A. .Effects of androgen administration in men with the AIDS wasting syndrome: a randomized, double-blind, placebo-controlled trial..Ann Intern Med 129: 18-26, 1998.
Crossref PubMed ISI Google Scholar

28. Hornum M , Cooper DM , Brasel JA , Bueno A , Sietsema KE. .Exercise-induced changes in circulating growth factors with cyclic variation in plasma estradiol in women..J Appl Physiol 82: 1946-1951, 1997.
Link ISI Google Scholar

29. Janowsky JS , Oviatt SK , Orwoll ES. .Testosterone influences spatial cognition in older men..Behav Neurosci 108: 325-332, 1994.
Crossref PubMed ISI Google Scholar

30. Katznelson L , Finkelstein JS , Schoenfeld DA , Rosenthal DI , Anderson EJ , Klibanski A. .Increase in bone density and lean body mass during testosterone administration in men with acquired hypogonadism..J Clin Endocrinol Metab 81: 4358-4365, 1996.
PubMed ISI Google Scholar

31. Kwan M , Greenleaf WJ , Mann J , Crapo L , Davidson JM. .The nature of androgen action on male sexuality: a combined laboratory- self-report study on hypogonadal men..J Clin Endocrinol Metab 57: 557-562, 1983.
Crossref PubMed ISI Google Scholar

32. Lugg JA , Rajfer J , Gonzalez-Cadavid NF. .Dihydrotestosterone is the active androgen in the maintenance of nitric oxide-mediated penile erection in the rat..Endocrinology 136: 1495-1501, 1995.
Crossref PubMed ISI Google Scholar

33. Mauras N , Hayes V , Welch S , Veldhuis J , Urban R. .Testosterone deficiency in young men: marked alterations in whole body protein kinetics, strength, and adiposity..J Clin Endocrinol Metab83: 1886-1892, 1998.
PubMed ISI Google Scholar

34. Meikle AW , Arver S , Dobs AS , Adolfsson J , Sanders SW , Middleton RG , Stephenson RA , Hoover DR , Rajaram L , Mazer NA. .Prostate size in hypogonadal men treated with a nonscrotal permeation-enhanced testosterone transdermal system..Urology 49: 191-196, 1997.
Crossref PubMed ISI Google Scholar

35. Naets JP , Wittek M. .Mechanism of action of androgens on erythropoiesis..Am J Physiol210: 315-320, 1966.
Abstract ISI Google Scholar

36. Negro-Vilar A. .Selective androgen receptor modulators (SARMs): a novel approach to androgen therapy for the new millennium..J Clin Endocrinol Metab 84: 3459-34362, 1999.
Crossref PubMed ISI Google Scholar

37. Pavlou SN , Brewer K , Farley MG , Lindner J , Bastias MC , Rogers BJ , Swift LL , Rivier JE , Vale WW , Conn PM. .Combined administration of a gonadotropin-releasing hormone antagonist and testosterone in men induces reversible azoospermia without loss of libido..J Clin Endocrinol Metab 73: 1360-1369, 1991.
Crossref PubMed ISI Google Scholar

38. Pope HG , Jacobs A. .Evidence for sex-specific residual effect of cannabis on visuo-spatial memory..Psychother Psychosom 66: 179-184, 1997.
Crossref PubMed ISI Google Scholar

39. Rance NE , Max SR. .Modulation of the cytosolic androgen receptor in striated muscle by sex-steroids..Endocrinology 115: 862-866, 1984.
Crossref PubMed ISI Google Scholar

40. Rencricca NJ , Solomon J , Fimian WJ , Howard D , Rizzoli V , Stohlman F .The effect of testosterone on erythropoiesis..Scand J Haematol 6: 431-436, 1969.
PubMed Google Scholar

41. Salmimies P , Kockott G , Pirke KM , Vogt HJ , Schill WB. .Effects of testosterone replacement on sexual behavior in hypogonadal men..Arch Sex Behav 11: 345-353, 1982.
Crossref PubMed ISI Google Scholar

42. Siebers RW , Carter JM , Maling TJ. .Increase in haematocrit in borderline hypertensive men..Clin Exp Pharmacol Physiol 21: 401-403, 1994.
Crossref PubMed ISI Google Scholar

43. Sinha-Hikim I , Arver S , Beall G , Shen R , Guerrero M , Sattler F , Shikuma C , Nelson JC , Landgren BM , Mazer NA , Bhasin S. .The use of a sensitive, equilibrium dialysis method for the measurement of free testosterone levels in healthy, cycling women, and in HIV-infected women..J Clin Endocrinol Metab 83: 1312-1318, 1998.
PubMed ISI Google Scholar

44. Snyder PJ , Lawrence DA. .Treatment of male hypogonadism with testosterone enanthate..J Clin Endocrinol Metab 51: 1335-1339, 1980.
Crossref PubMed ISI Google Scholar

45. Snyder PJ , Peachey H , Berlin JA , Hannoush P , Haddad G , Dlewati A , Santanna J , Loh L , Lenrow DA , Holmes JH , Kapoor SC , Atkinson JE , Strom BLE .Effects of testosterone replacement in hypogonadal men..J Clin Endocrinol Metab85: 2670-2677, 2000.
PubMed ISI Google Scholar

46. Snyder PJ , Peachey H , Hannoush P , Berlin JA , Loh L , Lenrow DA , Holmes JH , Dlewati A , Santanna J , Rosen CJ , Strom BL. .Effect of testosterone treatment on body composition and muscle strength in men over 65 years of age..J Clin Endocrinol Metab 84: 2647-2653, 1999.
PubMed ISI Google Scholar

47. Tenover JS. .Androgen replacement therapy to reverse and/or prevent age-associated sarcopenia in men..Bailliere’s Clin Endocrinol Metab 12: 419-425, 1998.
Crossref PubMed ISI Google Scholar

48. Van Goozen SH , Cohen-Kettenis PT , Gooren LJ , Frijda NH , Van de Poll NE. .Activating effects of androgens on cognitive performance: causal evidence in a group of female-to-male transsexuals..Neuropsychologia 32: 1153-1157, 1994.
Crossref PubMed ISI Google Scholar

49. Wang C , Swedloff RS , Iranmanesh A , Dobs A , Snyder PJ , Cunningham G , Matsumoto AM , Weber T , Berman N. .Transdermal testosterone gel improves sexual function, mood, muscle strength, and body composition parameters in hypogonadal men. Testosterone Gel Study Group..J Clin Endocrinol Metab 85: 2839-2853, 2000.
PubMed ISI Google Scholar

50. Wilson JD. .Androgen abuse by athletes..Endocr Rev 9: 181-199, 1988.







Authors – Shalender Bhasin,  Linda Woodhouse, Richard Casaburi, Atam B. Singh, Dimple Bhasin, Nancy Berman, Xianghong Chen, Kevin E. Yarasheski, Lynne Magliano, Connie Dzekov, Jeanne Dzekov, Rachelle Bross, Jeffrey Phillips, Indrani Sinha-Hikim. Ruoquing Shen and Thomas W.