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Effect of adolescent androgen manipulation on psychosis-like behaviour in adulthood in BDNF heterozygous and control mice.
Du, X; McCarthny, C R; Notaras, M; van den Buuse, M; Hill, R A.
Afiliação
  • Du X; Department of Psychiatry, Monash University, Melbourne, Australia.
  • McCarthny CR; The Florey Institute of Neuroscience and Mental Health, University of Melbourne, Australia.
  • Notaras M; Center for Neurogenetics, Brain & Mind Research Institute, Cornell University, NY, USA.
  • van den Buuse M; School of Psychology and Public Health, La Trobe University, Melbourne, Australia; Department of Pharmacology, University of Melbourne, Australia; The College of Public Health, Medical and Veterinary Sciences, James Cook University, Townsville, Australia. Electronic address: m.vandenbuuse@latrobe.ed
  • Hill RA; Department of Psychiatry, Monash University, Melbourne, Australia.
Horm Behav ; 112: 32-41, 2019 06.
Article em En | MEDLINE | ID: mdl-30928609
ABSTRACT
RATIONALE Males are more prone to psychosis, schizophrenia and substance abuse and addiction in adolescence and early adulthood than females. However, the role of androgens during this developmental period is poorly understood.

OBJECTIVES:

This study aimed to examine how androgens in adolescence influence psychosis-like behaviour in adulthood and whether brain-derived neurotrophic factor (BDNF) is a mediator of these developmental effects.

METHODS:

Wild-type and BDNF heterozygous male mice were castrated at pre-pubescence and implanted with testosterone or dihydrotestosterone (DHT). In adulthood, we assessed amphetamine- and MK-801-induced hyperlocomotion as a model of psychosis-like behaviour. Western blot analysis was used to quantify levels of the dopamine transporter (DAT) and N-methyl-d-aspartate (NMDA) receptor subunits.

RESULTS:

While castration itself had little effect on behaviour, adolescent testosterone, but not DHT, significantly reduced amphetamine-induced hyperlocomotion, whereas both testosterone and DHT reduced the effect of MK-801. These effects were similar in mice of either genotype. In wildtype mice, both testosterone and DHT treatment reduced DAT expression in the medial prefrontal cortex (mPFC) but these effects were absent in BDNF heterozygous mice. There were no effects on NMDA receptor subunit levels.

CONCLUSIONS:

The differential effect of adolescent testosterone and DHT on amphetamine-induced hyperlocomotion in adulthood suggests involvement of conversion of testosterone to estrogen and subsequent modulation of dopaminergic signalling. In contrast, the similar effect of testosterone and DHT treatment on NMDA receptor-mediated hyperlocomotion indicates it is mediated by androgen receptors. The involvement of BDNF in these hormone effects remains to be elucidated. These results demonstrate that, during adolescence, androgens significantly influence key pathways related to various mental illnesses prevalent in adolescence.
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Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 1_ASSA2030 Base de dados: MEDLINE Assunto principal: Transtornos Psicóticos / Maturidade Sexual / Comportamento Animal / Fator Neurotrófico Derivado do Encéfalo / Androgênios Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Revista: Horm Behav Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 1_ASSA2030 Base de dados: MEDLINE Assunto principal: Transtornos Psicóticos / Maturidade Sexual / Comportamento Animal / Fator Neurotrófico Derivado do Encéfalo / Androgênios Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Revista: Horm Behav Ano de publicação: 2019 Tipo de documento: Article