The Effects of Supraphysiologic Doses of Testosterone on Muscle Size and Strength in Normal Men
Shalender Bhasin, M.D., Thomas W. Storer, Ph.D., Nancy Berman, Ph.D., Carlos Callegari, M.D., Brenda Clevenger, B.A., Jeffrey Phillips, M.D., Thomas J. Bunnell, B.A., Ray Tricker, Ph.D., Aida Shirazi, R.Ph., and Richard Casaburi, Ph.D., M.D.
Background Athletes often take androgenic steroids in an attemptto increase their strength. The efficacy of these substancesfor this purpose is unsubstantiated, however.
Methods We randomly assigned 43 normal men to one of four groups:placebo with no exercise, testosterone with no exercise, placeboplus exercise, and testosterone plus exercise. The men receivedinjections of 600 mg of testosterone enanthate or placebo weeklyfor 10 weeks. The men in the exercise groups performed standardizedweight-lifting exercises three times weekly. Before and afterthe treatment period, fat-free mass was determined by underwaterweighing, muscle size was measured by magnetic resonance imaging,and the strength of the arms and legs was assessed by bench-pressand squatting exercises, respectively.
Results Among the men in the no-exercise groups, those giventestosterone had greater increases than those given placeboin muscle size in their arms (mean [±SE] change in tricepsarea, 424±104 vs. -81±109 mm2; P<0.05) andlegs (change in quadriceps area, 607±123 vs. -131±111mm2; P<0.05) and greater increases in strength in the bench-press(9±4 vs. -1±1 kg, P<0.05) and squatting exercises(16±4 vs. 3±1 kg, P<0.05). The men assignedto testosterone and exercise had greater increases in fat-freemass (6.1±0.6 kg) and muscle size (triceps area, 501±104mm2; quadriceps area, 1174±91 mm2) than those assignedto either no-exercise group, and greater increases in musclestrength (bench-press strength, 22±2 kg; squatting-exercisecapacity, 38±4 kg) than either no-exercise group. Neithermood nor behavior was altered in any group.
Conclusions Supraphysiologic doses of testosterone, especiallywhen combined with strength training, increase fat-free massand muscle size and strength in normal men.
Anabolicandrogenic steroids are widely abused by athletesand recreational bodybuilders because of the perception thatthese substances increase muscle mass and strength,1-9 but thispremise is unsubstantiated. Testosterone replacement increasesnitrogen retention and fat-free mass in castrated animals andhypogonadal men,10-15 but whether supraphysiologic doses oftestosterone or other anabolicandrogenic steroids augmentmuscle mass and strength in normal men is unknown.1-9 Studiesof the effects of such steroids on muscle strength have beeninconclusive,16-33 and several reviews have emphasized the shortcomingsof the studies.1-5,8-10 Some of the studies were not randomized;most did not control for intake of energy and protein; the exercisestimulus was often not standardized; and some studies includedcompetitive athletes whose motivation to win may have kept themfrom complying with a standardized regimen of diet and exercise.
We sought to determine whether supraphysiologic doses of testosterone,administered alone or in conjunction with a standardized programof strength-training exercise, increase fat-free mass and musclesize and strength in normal men. To overcome the pitfalls ofprevious studies, the intake of energy and protein and the exercisestimulus were standardized. Because some previous studies haddemonstrated significant increases in muscle strength and hypertrophyin experienced athletes but not in sedentary subjects, we studiedmen who had weight-lifting experience.
Methods
Study Design
This study was approved by the institutional review boards ofthe HarborUCLA Research and Education Institute and theCharles R. Drew University of Medicine and Science. All thestudy subjects gave informed written consent. The subjects werenormal men weighing 90 to 115 percent of their ideal body weights;they were 19 to 40 years of age and had experience with weightlifting. They were recruited through advertisements in localnewspapers and community colleges. None had participated incompetitive sports in the preceding 12 months. Men who had evertaken anabolic agents or recreational drugs or had had a psychiatricor behavioral disorder were excluded from the study.
Of 50 men who were recruited, 7 dropped out during the controlperiod because of problems with scheduling or compliance. Theremaining 43 men were randomly assigned to one of four groups:placebo with no exercise, testosterone with no exercise, placeboplus exercise, and testosterone plus exercise. The study wasdivided into a 4-week control period, a 10-week treatment period,and a 16-week recovery period. During the four-week controlperiod, the men were asked not to lift any weights or engagein strenuous aerobic exercise.
Of the 43 men, 3 dropped out during the treatment phase: 1 becauseof problems with compliance, 1 because illicit-drug use wasdetected by routine drug screening, and 1 because of an automobileaccident. Forty men completed the study: 10 in the placebo,no-exercise group; 10 in the testosterone, no-exercise group;9 in the placebo-plus-exercise group; and 11 in the testosterone-plus-exercisegroup.
Standardization of Protein and Energy Intake
Two weeks before day 1, the men were instructed to begin followinga standardized daily diet containing 36 kcal per kilogram ofbody weight, 1.5 g of protein per kilogram, and 100 percentof the recommended daily allowance of vitamins, minerals, andtrace elements. Compliance with the diet was verified everyfour weeks by three-day records of food consumption. The dietaryintake was adjusted every two weeks on the basis of changesin body weight.
Treatment
The men received either 600 mg of testosterone enanthate insesame oil or placebo intramuscularly each week for 10 weeksin the Clinical Research Center. This dose is six times higherthan the dose usually given as replacement therapy in men withhypogonadism and is therefore supraphysiologic. Doses as highas 300 mg per week have been given to normal men for 16 to 24weeks without major toxic effects.34
Training Stimulus
The men in the exercise groups received controlled, supervisedstrength training three days per week during the treatment period.All the men trained at equivalent intensities in relation totheir strength scores before the training. The training consistedof a cycle of weight lifting at heavy intensity (90 percentof the maximal weight the man lifted for one repetition beforethe start of training), light intensity (70 percent of the pretrainingone-repetition maximal weight), and medium intensity (80 percentof this maximal weight) on three nonconsecutive days each week.35Regardless of the actual weights lifted, the training was heldconstant at four sets with six repetitions per set (a set isthe number of complete repetitions of an exercise followed byrest). Because previous research had demonstrated increasesin strength of approximately 7 percent for the bench-press exerciseand 12 percent for the squatting exercise after four to fiveweeks of training,35 the weights were increased correspondinglyduring the final five weeks of training in relation to the initialintensity. The number of sets was also increased from four tofive, but the number of repetitions per set remained constant.The men were advised not to undertake any resistance exerciseor moderate-to-heavy endurance exercise in addition to the prescribedregimen.
Evaluation and Outcome Measures
The primary end points were fat-free mass, muscle size as measuredby magnetic resonance imaging (MRI), and muscle strength asbased on the one-repetition maximal weight lifted during thebench-press and squatting exercises before and after the 10-weektreatment period. Serum concentrations of total and free testosterone,luteinizing hormone, follicle-stimulating hormone, and sex hormonebindingglobulin were measured on days 14 and 28 of the control periodand days 2, 3, 7, 14, 28, 42, 56, and 70 of the treatment period.Blood counts, blood chemistry (including serum aminotransferases),serum concentrations of prostate-specific antigen, and plasmaconcentrations of total cholesterol, low-density lipoprotein(LDL) cholesterol, high-density lipoprotein (HDL) cholesterol,and triglycerides were measured at the start of the controlperiod and on day 4; on days 28, 56, and 70 of the treatmentperiod; and four months after the discontinuation of treatment.Periodic evaluations to identify adverse effects were performedby examiners unaware of the study-group assignments on days1 and 28 of the control period; days 28, 56, and 70 of the treatmentperiod; and four months after the discontinuation of treatment.Mood and behavior were evaluated during the first week of thecontrol period and after 6 and 10 weeks of treatment. Sexualfunction and semen characteristics were not assessed.
Assessment of Muscle Size
Muscle size was measured by MRI of the arms and legs at thehumeral or femoral mid-diaphyseal level, the junction of theupper third and middle third of the bone, and the junction ofthe middle third and lower third. The cross-sectional areasof the arms and legs, the subcutaneous tissue, the muscle compartment,and the quadriceps and triceps muscles were computed, and theareas at the three levels were averaged.
Analysis of Body Composition
Fat-free mass was estimated on the basis of measurements ofbody density obtained by underwater weighing. During weighing,the men were asked to exhale to the residual volume, as measuredby helium dilution.
Measures of Muscle Strength
The effort-dependent performance of muscle was assessed on thebasis of the maximal weight lifted for one repetition duringthe bench-press and squatting exercises.36 Each man completedincreasingly more difficult lifts with the same weights andbars that he used during training; in each exercise, the maximalweight lifted (the one-repetition maximum) was recorded as ameasure of muscle strength.
Hormone Measurements
Serum concentrations of luteinizing hormone and follicle-stimulatinghormone were measured by immunofluorometric assays,36 each witha sensitivity of 0.05 IU per liter. Serum testosterone was measuredby immunoassay,37 and free testosterone was measured by equilibriumdialysis.37 Serum concentrations of sex hormonebindingglobulin and prostate-specific antigen were measured by immunoassaysusing reagents purchased from DelphiaWallac (Turku, Finland)and Hybritech (San Diego, Calif.), respectively.
Assessment of Mood and Behavior
A standardized Multidimensional Anger Inventory38 that includes38 questions to measure the frequency, duration, magnitude,and mode of expression of anger, arousal of anger, hostile outlook,and anger-eliciting situations and a Mood Inventory that includesquestions pertaining to general mood, emotional stability, andangry behavior were administered before, during (week 6), andafter the treatment (unpublished data). For each man a live-inpartner, spouse, or parent answered the same questions aboutthe man's mood and behavior.
Statistical Analysis
The Shapiro and Wilk test was used to test whether the outcomevariables had a normal distribution. Changes were computed foreach subject as the difference between the values for each variableat the beginning and end of the treatment period (from day 0to day 70). These values were averaged among the subjects ineach group to obtain the group means. Analysis of variance wasused to determine whether there were base-line differences amongthe four groups. Two-tailed, paired t-tests were used to testfor changes in each outcome variable in each group. If therewas a change, an analysis of variance was used to test for differencesbetween groups in the amount of change, and then Scheffé'stest was used to assess pairwise differences. This test adjustsfor multiple comparisons, but it does not yield exact P valuesfor pairwise comparisons between groups.
Results
The four groups were similar with respect to age and weight,height, and body-mass index before treatment (Table 1). Acnedeveloped in three men receiving testosterone and one receivingplacebo, and two men receiving testosterone reported breasttenderness, but no other side effects were noted. The serumliver-enzyme concentrations, hemoglobin concentrations, hematocrits,and red-cell counts did not change in any study group (Table 2).Serum creatinine concentrations did not change, except inthe testosterone-plus-exercise group, in which the mean (±SE)serum creatinine concentration increased from 1.0 mg per deciliter(88 µmol per liter) to 1.1 mg per deciliter (97 µmolper liter) (P=0.02). Plasma concentrations of total and LDLcholesterol and triglycerides did not change in any study group;plasma HDL cholesterol decreased significantly in the placebo-plus-exercisegroup. There was no change in the serum concentration of prostate-specificantigen in any group.
Table 2. Hemoglobin and Plasma Lipid Concentrations before and after the 10 Weeks of Treatment.
Endocrine Responses
The base-line serum concentrations of total and free testosteronein the four groups were similar. The serum concentrations oftotal and free testosterone increased significantly in the twotestosterone groups, but not in the placebo groups (Table 3).The base-line serum concentrations of luteinizing hormone, follicle-stimulatinghormone, and sex hormonebinding globulin were similarin the four groups, and the concentrations decreased significantlyin the two testosterone groups.
Table 3. Serum Concentrations of Endocrine Hormones in the Study Subjects before and after the 10 Weeks of Treatment.
Body Weight and Composition
Body weight did not change significantly in the men in eitherplacebo group (Table 4). The men given testosterone withoutexercise had a significant mean increase in total body weight,and those in the testosterone-plus-exercise group had an averageincrease of 6.1 kg in body weight a greater increasethan in the other three groups.
Table 4. Body Weight, Fat-free Mass, and Muscle Size and Strength before and after the 10 Weeks of Treatment.
Fat-free mass did not change significantly in the group assignedto placebo but no exercise (Table 4 and Figure 1). The men treatedwith testosterone but no exercise had an increase of 3.2 kgin fat-free mass, and those in the placebo-plus-exercise grouphad an increase of 1.9 kg. The increase in the testosterone-plus-exercisegroup was substantially greater (averaging 6.1 kg). The percentageof body fat did not change significantly in any group (datanot shown).
Figure 1. Changes from Base Line in Mean (±SE) Fat-free Mass, Triceps and Quadriceps Cross-Sectional Areas, and Muscle Strength in the Bench-Press and Squatting Exercises over the 10 Weeks of Treatment.
The P values shown are for the comparison between the change indicated and a change of zero. The asterisks indicate P<0.05 for the comparison between the change indicated and that in either no-exercise group; the daggers, P<0.05 for the comparison between the change indicated and that in the group assigned to placebo with no exercise; and the double daggers, P<0.05 for the comparison between the change indicated and the changes in all three other groups.
Muscle Size
The mean cross-sectional areas of the arm and leg muscles didnot change significantly in the placebo groups, whether themen had exercise or not (Table 4 and Figure 1). The men in thetestosterone groups had significant increases in the cross-sectionalareas of the triceps and the quadriceps (Table 4); the groupassigned to testosterone without exercise had a significantlygreater increase in the cross-sectional area of the quadricepsthan the placebo-alone group, and the testosterone-plus-exercisegroup had greater increases in quadriceps and triceps area thaneither the testosterone-alone or the placebo-plus-exercise group(P<0.05).
Muscle Strength
Muscle strength in the bench-press and the squatting exercisesdid not change significantly over the 10-week period in thegroup assigned to placebo with no exercise. The men in the testosterone-aloneand placebo-plus-exercise groups had significant increases inthe one-repetition maximal weights lifted in the squatting exercises,averaging 19 percent and 21 percent, respectively (Table 4 andFigure 1). Similarly, mean bench-press strength increased inthese two groups by 10 percent and 11 percent, respectively.In the testosterone-plus-exercise group, the increase in musclestrength in the squatting exercise (38 percent) was greaterthan that in any other group, as was the increase in bench-pressstrength (22 percent).
Mood and Behavior
No differences were found between the exercise groups and theno-exercise groups or between the placebo groups and the testosteronegroups in any of the five subcategories of anger assessed bythe Multidimensional Anger Inventory. No significant changesin mood or behavior were reported by the men on the Mood Inventoryor by their live-in partners, spouses, or parents on the ObserverMood Inventory.
Discussion
Our results show that supraphysiologic doses of testosterone,especially when combined with strength training, increase fat-freemass, muscle size, and strength in normal men when potentiallyconfounding variables, such as nutritional intake and exercisestimulus, are standardized. The combination of strength trainingand testosterone produced greater increases in muscle size andstrength than were achieved with either intervention alone.The combined regimen of testosterone and exercise led to anincrease of 6.1 kg in fat-free mass over the course of 10 weeks;this increase entirely accounted for the changes in body weight.
The exercise was standardized in all the men, and thereforethe effects of testosterone on muscle size and strength cannotbe attributed to more intense training in the groups receivingthe treatment. Careful selection of experienced weight lifters,the exclusion of competitive athletes, and close follow-up ensureda high degree of compliance with the regimens of exercise, treatment,and diet, which was verified by three-day food records (datanot shown) and the values obtained for serum testosterone, luteinizinghormone, and follicle-stimulating hormone. Except for one manwho missed one injection, all the men received all their scheduledinjections. It has been argued that studies in which large dosesof androgens are used cannot be truly blinded because of theoccurrence of acne or other side effects. In this study, neitherthe investigators nor the personnel performing the measurementsknew the study-group assignments. Three men receiving testosteroneand one man receiving placebo had acneiform eruptions; thesemen may have assumed themselves to be receiving testosterone.Thus, it cannot be stated with certainty that the men were completelyunaware of the nature of their treatments.
The doses of androgenic steroids used in previous studies werelow,1-5,11,12 mostly because of concern about potential toxiceffects. In contrast, to our knowledge the dose of testosteroneenanthate administered in this study (600 mg per week) is thehighest administered in any study of athletic performance. Undoubtedly,some athletes and bodybuilders take even higher doses than thosewe gave. Furthermore, athletes often "stack" androgenic andanabolic steroids, taking multiple forms simultaneously. Wedo not know whether still higher doses of testosterone or thesimultaneous administration of several steroids would have morepronounced effects. The absence of systemic toxicity duringtestosterone treatment was consistent with the results of studiesof the contraceptive efficacy of that hormone.34
The method used in this study to evaluate muscle performanceon the basis of the one-repetition maximal weight lifted isdependent on effort. Although the men receiving testosteronedid have increases in muscle size, some of the gains in strengthmay have resulted from the behavioral effects of testosterone.
The dose dependency of the action of testosterone on fat-freemass and protein synthesis has not been well studied. Forbes39proposed a single doseresponse curve extending from thehypogonadal to the supraphysiologic range. Others have suggestedthat there may be two doseresponse curves: one in thehypogonadal range, with maximal responses corresponding to theserum testosterone concentrations at the lower end of the rangein normal men, and the second in the supraphysiologic range,presumably representing a separate mechanism of action that is, a pathway of independent androgen receptors.1,40
Supraphysiologic doses of testosterone, with or without exercise,did not increase the occurrence of angry behavior by these carefullyselected men in the controlled setting of this experiment. Ourresults, however, do not preclude the possibility that stillhigher doses of multiple steroids may provoke angry behaviorin men with preexisting psychiatric or behavioral problems.
Our results in no way justify the use of anabolicandrogenicsteroids in sports, because, with extended use, such drugs havepotentially serious adverse effects on the cardiovascular system,prostate, lipid metabolism, and insulin sensitivity. Moreover,the use of any performance-enhancing agent in sports raisesserious ethical issues. Our findings do, however, raise thepossibility that the short-term administration of androgensmay have beneficial effects in immobilized patients, duringspace travel, and in patients with cancer-related cachexia,disease caused by the human immunodeficiency virus, or otherchronic wasting disorders.
Supported by a grant (1 RO1 DK 45211) from the National Institutesof Health, by a General Clinical Research Center grant (MO-00543),and by grants (P20RR11145-01, a Clinical Research InfrastructureInitiative; and G12RR03026) from the Research Centers for MinorityInstitutions.
We are indebted to Dr. Indrani Sinha-Hikim for the serum hormoneassays, to Dr. Paul Fu for the plasma lipid measurements, tothe staff of the General Clinical Research Center for conductingthe studies, and to BioTechnology General Corporation, Iselin,New Jersey, for providing testosterone enanthate.
Source Information
From the Department of Medicine, Charles R. Drew University of Medicine and Science, Los Angeles (S.B., C.C., B.C.); the Exercise Science Laboratory, El Camino College, Torrance, Calif. (T.W.S., T.J.B.); the Department of Medicine, HarborUCLA Medical Center, Torrance, Calif. (N.B., J.P., R.C.); and the Department of Public Health, Oregon State University, Corvallis (R.T., A.S.).
Address reprint requests to Dr. Bhasin at the Division of Endocrinology, Metabolism and Molecular Medicine, Charles R. Drew University of Medicine and Science, 1621 E. 120th St., MP #2, Los Angeles, CA 90059.
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