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You are here: Home / Steroid Articles / Psychological and Behavioural Effects of Endogenous Testosterone Levels and Anabolic-Androgenic Steroids Among Males: A Review, Part 4

Psychological and Behavioural Effects of Endogenous Testosterone Levels and Anabolic-Androgenic Steroids Among Males: A Review, Part 4

January 19, 1997 by Michael Bahkre, Charles Yesalis and James Wright 14 Comments

Brain on steroids

4. Anabolic Steroid Therapy and Moods

Hermann and Beach (1976), in a review of the psychotropic effects of androgens, concluded that ‘…androgen deficiency appears to cause a slowing down of both physical and mental functions, a reduction in libido and potency, and a tendency towards moodiness and depression. Conversely, androgen excess seems to stimulate physical and mental function, and to induce assertiveness rather than passivity, although the degree to which these people are overtly aggressive is somewhat unclear.’ Hermann and Beach also concluded that, ‘As yet no work, to our knowledge, has been done on the possible contribution that the reported variations in hormone levels make to the changed behaviour of those who become mentally disordered, nor to their exact role in metabolic changes which are supposed to accompany such illness.’ Unfortunately, although a number of studies have been conducted over the intervening years, little can be added to their conclusion at this point in time. This following section summarises research and clinical observations and effects in individuals with androgen deficiencies receiving androgen therapy.

Franchi et al. (1978) reported a marked increase in libido and sexual, physical and/or mental activities in all 34 hypogonadal male patients (18 to 49 years) given testosterone undecanoate (40 to 60 mg/day, orally) for 8 months when compared with a withdrawal period (3 weeks). Unfortunately, no information concerning the questionnaires used to assess the behavioural and mood changes is provided. No side effects were reported by any of the patients throughout the 8 months of therapy.

Franchimont et al. (1978) found improved mental and physical activity at 3-week intervals over 9 weeks in 7 and 2 of 10 hypogonadal male patients (16 to 51 years), respectively, undergoing therapy with oral testosterone undecanoate (120 to 240 mg/day). Again, no information is provided concerning how behavioural and mood changes were measured.

Luisi and Franchi (1980) in a double-blind, randomised, group comparative study of testosterone undecanoate (120 mg/day orally) and mesterolone (150 mg/day orally) in hypogonadal male patients found that testosterone undecanoate but not mesterolone induced a marked improvement in both sexual activity and mental state (unpublished modified Koch’s Mood Questionnaire) after 2 weeks. These improvements continued for the duration of the 4-week study. No side effects were reported in either group of patients. Using the Lorr and McNair Mood Check List in a double-blind crossover design, Skakkebaek et al. (1981) found significantly improved self-ratings of tension/anxiety and fatigue, a higher level of vigour, but no change in depression with androgen replacement (testosterone undecanoate 160 mg/day orally) versus placebo capsules (oleic acid) in 6 hypergonadotrophic (castration or primary testicular failure) and 6 hypogonadotrophic (hypothalamic or pituitary deficiency) men with hypogonadism. The study was conducted over a 4-month period (2 months on placebo and 2 months on testosterone undecanoate). In addition, there was a significant reduction in self-rated anger during testosterone administration. O’Carroll et al. (1985) also reported significantly improved well-being (4 of 10 self-reported visual analogue scales) with androgen replacement (testosterone undecanoate) in 8 hypogonadal men. A significant does response relationship for well-being was demonstrated with increasing doses (40, 80, 120, 160 mg/day orally) over 4 months.

Wu et al. (1982) using a double blind crossover design and the Lorr and McNair Mood Adjective Check List found no significant change in self-reported mood (anxiety/tension, depression, anger, vigour, fatigue) or energy in 4 adult men (30 to 48 years) with Klinefelters syndrome, low normal testosterone levels and normal sexual activity and interest given testosterone undecanoate (160 mg/day orally) for 8 weeks compared to placebo (8 weeks) and a baseline period of no treatment (8 weeks).

In a double-blind experiment, Davidson et al. (1979) found no consistent relationship between mood (Profile of Mood States) and androgen administration in 6 adult hypogonadal males receiving testosterone enanthate (100 or 400 mg/month in 2 doses) and a placebo treatment in randomly assigned 4-week periods over a 5-month period. Although frequencies of erections showed significant dose-related responses which closely followed the fluctuations in the serum testosterone levels, individual records showed only 1 clear instance of change in mood (POMS) related to treatment (1 subject showed peak increases in anger 1 week after receiving treatment after guessing that he was on placebo). Salmimies et al. (1982) also found no significant differences in biweekly mood ratings when comparing 15 adult hypogonadal male patients administered increasing doses of testosterone enanthate (25, 50, 100, 250mg or placebo) injected over a 5-month period. Each dose was given twice (every 2 weeks) over 4 weeks.

Results from the preceding studies are mixed (table II). Some demonstrate significant positive psychological changes with anabolic-androgenic steroids, others do not. However, no adverse or undesired psychological or behavioural effects were observed in these studies. Interestingly, 5 of the 6 studies which administered oral androgens reported improved mood states following therapy (with the exception of the mesterolone group of Luisi and Franchi); the results of the 2 studies using intramuscular injections of various testosterone esters found no change. However, it should be noted that only perhaps 1 or 2 of the doses administered in these 2 studies (200mg biweekly and 250mg biweekly) would restore and maintain normal physiological testosterone levels and full androgenic function for the entire duration between injections.

O’Carroll and Bancroft (1984), in a carefully controlled double-blind crossover comparison of biweekly injections of 250mg of testosterone esters (‘Sustanon’) or placebo in 2 groups of men (n=20) with normal testosterone levels, likewise found no significant change in mood ratings (10 self-reported visual analogue scales) following 12 weeks of treatment (half the subjects in each group received 6 weeks of testosterone followed by 6 weeks placebo, and the other half vice versa).

Part 5: Steroids and Mental Health

Originally appearing in Sports Medicine 10(5) 303-337. 1990. Copyright © 1990 by Adis International Limited. All rights reserved. Reprinted by MESO-Rx with permission. Any duplication of this document by electronic or other means is strictly prohibited.

About the author


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Michael Bahrke
Michael Bahkre
Science consultant at Health, Fitness, and Wellness, Ellison Bay

Michael S. Bahrke, BS, MS, PhD, US, master's degree in exercise physiology and a doctorate in sport psychology. Bahrke has been an assistant professor at the University of Kansas, director of research for the US Army Physical Fitness School, and project director for a National Institute on Drug Abuse-funded anabolic steroid research grant at the University of Illinois in Chicago. Authored and co-authored more than 80 scientific publications and has made presentations at numerous scientific meetings, including the International Conference on the Abuse and Trafficking of Anabolic Steroids, sponsored by the US Drug Enforcement Administration; the American Psychological Association; and the American Psychiatric Association.

Charles Yesalis
Charles Yesalis
Professor Emeritus of Health Policy and Administration at Pennsylvania State University

Dr. Yesalis' research has been devoted to the non-medical use of anabolic-androgenic steroids (AS) and other performance-enhancing drugs and dietary supplements. In 1988 he directed the first national study of AS use among adolescents and was the first to present evidence of psychological dependence on AS. In addition, he has studied the incidence of AS use among elite power lifters, collegiate athletes, and professional football players. In 1998 he wrote The Steroids Game which focuses on prevention, education, and intervention regarding AS use by adolescents. He is the editor of a medical reference text, Anabolic Steroids in Sport and Exercise (2nd ed.) and co-editor of Performance Enhancing Substances in Sport and Exercise.

James E. Wright
James Wright
Exercise physiologist at Sports Science Consultants

James E. Wright, PhD., is widely acknowledged as one of the world's leading authorities on anabolic steroids. He has authored and co-authored several books on the topic including Anabolic Steroids and Sports, Volumes I and II and Altered States: The Use and Abuse of Anabolic Steroids.

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Avatar of Eman Eman Jan 23, 2022 #1

"Joslyn (1973) has reported that injecting 3 infant female rhesus monkeys with 2mg of testosterone propionate intramuscularly 3 times per week over 8 months increased their aggressive behaviour so much so that they replaced males in top positions of the social hierarchy. Since this behaviour persisted for a year after the last hormone injection, the author suggests either that the male hormone may have directly induced a permanent change in the nervous system or alternatively that the socially dominant behaviour was so well learned during hormone treatment that it became independent of hormonal support."

That is fascinating.

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Avatar of Type-IIx Type-IIx Jan 23, 2022 #2

T seems to increase aggression by reduced activation of the orbitofrontal cortex, the neural circuitry of impulse control and self-regulation. But note that the effect size of T on a model of social aggression in humans is very small (r=0.35; barely significant). Higher testosterone in humans is related to aggression, social dominance, and hyperreactivity to status threats in both men and women. I have remarked before that I have a strong supposition that this is at the root of the romantic paranoia that users of tren often report (being "cucked" is the ultimate status threat).

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Avatar of Type-IIx Type-IIx Jan 23, 2022 #3

The Hannan et al. (1988) findings are very interesting for explaining some of the widespread anecdotal reports of particular psychological effects with nandrolone.

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Avatar of Iamnatty Iamnatty Jan 23, 2022 #4

Where do you find this information at.

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Avatar of Mac11wildcat Mac11wildcat Jan 23, 2022 #5

What interests me is the varied psychological effects we see. Whether it’s just a variation of the original disposition of the user, the age at onset of use, or sensitivity to individual drugs themselves. Tren is the ‘obvious’ one, but EQ is getting quite a reputation for inducing anxiety.

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Avatar of Millard Millard Jan 24, 2022 #6

Yeah, the idea that permanent changes occur with limited AAS use is very interesting but also that researchers allowed for the possibility that the learned behavior is what changed the nervous system in the long-term.

I remember as a undergrad RA, my mentor was really excited by research showing that CBT could induce brain changes similar to that seen with meds.

I can totally see learned behavior (e.g. social/sexual confidence, etc) while on AAS persisting long after discontinuation in many users.

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Avatar of Millard Millard Jan 24, 2022 #7

It's in part 2 of the above article discussing ways AAS could affect the CNS.

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Avatar of Cherokee Cherokee Jan 24, 2022 #8


Cognitive Deficits in Long-Term Anabolic-Androgenic Steroid Users - PMC

Millions of individuals worldwide have used anabolic-androgenic steroids (AAS) to gain muscle or improve athletic performance. Recently, in vitro investigations have suggested that supraphysiologic AAS doses cause apoptosis of neuronal cells. These ...

View image at the forums


www.ncbi.nlm.nih.gov

preliminary findings raise the ominous possibility that long-term high-dose AAS exposure may cause cognitive deficits, notably in visuospatial memory.

Visuospatial function refers to cognitive processes necessary to "identify, integrate, and analyze space and visual form, details, structure and spatial relations" in more than one dimension.[1]

Visuospatial skills are needed for movement, depth and distance perception, and spatial navigation.[1] Impaired visuospatial skills can result in, for example, poor driving ability because distances are not judged correctly or difficulty navigating in space such as bumping into things.[1]

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Avatar of Eman Eman Jan 24, 2022 #9

Same. I think that's what really intrigues me by that paragraph... I mean, which is it?

I have wondered about this before. Many times in fact. I've always described it as "primal switches in the brain getting flipped". I have come to a passive conclusion that the switches get flipped on but they never actually get flipped back off even when the stimulus is gone.

Very cool collection of articles, I've never come across them before and I'm not familiar with any of those authors either. Really enjoy these older articles getting bumped!

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Avatar of Jin23 Jin23 Dec 13, 2022 #10

I had no idea meso had such roots. That's very nice to hear.

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Avatar of Rido Rido Dec 22, 2022 #11

UHH I gotta say. Tren is reminding me of nandrolone of me wanting to pound other women's pussy in and watch my wife have a train ran on her too...

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Avatar of lukiss96 lukiss96 Dec 22, 2022 #12

What I notice is probably different from most people, I get aggressive on equipoise stacked with test and calm on testosterone solo at any dose up to 1g.

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Avatar of T&H T&H Dec 22, 2022 #13

I've ran test, mast, primo, and a number of different orals at higher doses. Other than a few days of euphoria a few weeks into my first time using testosterone, I don't ever notice psychological changes when running AAS.

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Avatar of Type-IIx Type-IIx Dec 24, 2022 #14

Deviants are by definition deviations from the norm bro

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