Cited by 15Neuroendocrine regulation and behaviorSexual Differentiation and DisordersStress Responses and Cortisol

The influence of exogenous testosterone and corticosterone on the social behavior of prepubertal male rats

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Meaney, Michael J., Stewart, Jane·1983·Bulletin of the Psychonomic Society

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Crossref · 10.3758/bf03334695

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1 of 1 references verified0 citation errors · 0 not checkable

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  • Treating male rat pups with the androgen receptor antagonist flutamide during the critical period prevents the development of male-typical play, so these males play at the same level as females.

    “Similarly, treating male rat pups with the androgen receptor antagonist flutamide to block the actions of testosterone during the critical period prevents the development of male-typical play. As a result, these males play at the same level as females (Meaney et al., 1983).”

    From Developmental origins of sex differences in the neural circuitry of play (2020) · cites this paper as Meaney et al., 1983

    The paper’s introductory passage reports that castration of male pups on Day 1 or Day 6 reduced play-fighting to levels indistinguishable from those of females. It does not report flutamide treatment; the Method section describes injections of testosterone propionate, corticosterone, or oil instead. Thus the female-level play finding is supported for early castration, not for the claimed androgen-receptor blockade. (LLM, conf=0.88)

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  • Male rats with nonfunctional androgen receptors (Tfm males) engage in some aspects of play at male-typical levels.

    “Supporting this idea, male rats with nonfunctional androgen receptors, so-called “Tfm males”, engage in some aspects of play at male-typical levels (Meaney et al., 1983; Field et al., 2006).”

    From Developmental origins of sex differences in the neural circuitry of play (2020) · cites this paper as Meaney et al., 1983

    The Discussion reports that weanling-castrated males and intact males did not differ in play-fighting frequency. But neither the Discussion nor the Results addresses Tfm males or nonfunctional androgen receptors; the studied groups received testosterone propionate, corticosterone, or oil. The male-typical play comparison is supported for a different condition, not for Tfm males. (LLM, conf=0.84)

    Experimental — accuracy not yet measured
  • The development of male-typical play is largely androgen-dependent.

    “Initial studies investigating the sexual differentiation of play discovered that the development of male-typical play is actually largely androgen-dependent.”

    From Developmental origins of sex differences in the neural circuitry of play (2020) · cites this paper as Meaney et al., 1983

  • Treating female rat pups with testosterone or 5α-dihydrotestosterone during the sensitive period increases their play to male-typical levels.

    “Treating female rat pups with testosterone or 5α-dihydrotestosterone (a testosterone analog that cannot be converted into estradiol) during the sensitive period in development increases their play to male-typical levels.”

    From Developmental origins of sex differences in the neural circuitry of play (2020) · cites this paper as Meaney et al., 1983

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Cites

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Research works printed but not linked: 9

  1. BAUM. M. J. Precocious mating in male rats following treatment with androgen or estrogen. Journal of Comparative and Physio- logical Psychology, 1972. 71. 356-367.
  2. GOY, R. W. Development of play and mounting behavior in female rhesus virilized prenatally with esters of testosterone or dihydro- testosterone. In D. J. Chivers & J. Herbert (Eds.), Recent advances in primatology (Vol. 1). Behavior. New York: Academic Press, 1978.
  3. JOSLYN, W. D. Androgen-induced social dominance in infant female rhesus monkeys. Journal of Child Psychology and Psy- chiatry, 1973,14,137-145.
  4. KRUSKAL, W. H., & WALLIS, W. A. Use of ranks in one-criterion variance analysis. Journal of the American Statistical Associ- ation, 1952.47, 583-621.
  5. LEVY, J. V., & KING, J. A. The effects of testosterone propionate on fighting behavior in young male C56BLllO mice. Anatomi- cal Record, 1953, 117, 562-563.
  6. MEANEY, M. J., & STEWART, J., & BEATTY, W. W. The influence of neonatal glucocorticoids on the social play of prepubertal rats. Hormones and Behavior, 1982, 16,475-491.
  7. OLIOFF, M., & STEWART, J. Sex difference in the play behavior of prepubescent rats. Physiology & Behavior, 1978,20, 113-115.
  8. POOLE, T. B., & FISH, J. An investigation of individual. age. and sexual differences in the play of Rattus norvegicus (Mammalia: Rodentia). Proceedings of the Zoological Society of London, 1976, 179, 249-260.
  9. SEIGEL, S. Non-parametric statistics. McGraw-Hill: New York, 1"6.

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Authors
Meaney, M. J., & Stewart, J.
Affiliations
  • Rockefeller University (US)
  • Concordia University (CA)
Venue
Bulletin of the Psychonomic Society
Published
1983-03
Volume
21
Issue
3
Pages
232-234
ISSN
0090-5054 (ISSN-L)
OpenAlex
W2022132041
Cited by
15
References
1
Citations by year
2024: 2
FWCI
4.11
Type
journal article
Language
en
Open access
Locations
Bulletin of the Psychonomic Society (publishedVersion)
Topics
  • Social Sciences › Psychology › Social Psychology › Neuroendocrine regulation and behavior
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Sexual Differentiation and Disorders
  • Life Sciences › Neuroscience › Behavioral Neuroscience › Stress Responses and Cortisol
Keywords
testosterone propionate, corticosterone, social behavior, play fighting, dominance, submission, organizational effects, activational effects, prepubertal rats, androgens, glucocorticoids

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