Article (Scientific journals)
Inhibition of steroid receptor coactivator-1 blocks estrogen and androgen action on male sex behavior and associated brain plasticity.
Charlier, Thierry; Ball, Gregory F; Balthazart, Jacques
2005In Journal of Neuroscience, 25 (4), p. 906-13
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Keywords :
Androgen Antagonists; Androgens/physiology; aromatase; sexually dimorphic nucleus; Japanese quail; antisense; vasotocin; Animals; Aromatase/metabolism; Brain/metabolism/pathology/physiology; Coturnix; Estrogen Antagonists; Estrogens/physiology; Histone Acetyltransferases; Male; Neuronal Plasticity/physiology; Oligodeoxyribonucleotides, Antisense; Preoptic Area/physiology; Sexual Behavior, Animal/physiology; Testosterone/antagonists & inhibitors/physiology; Transcription Factors/antagonists & inhibitors/physiology
Abstract :
[en] Studies of eukaryotic gene expression demonstrate the importance of nuclear steroid receptor coactivators in mediating efficient gene transcription. However, little is known about the physiological role of these coactivators in vivo. In Japanese quail, the steroid receptor coactivator-1 (SRC-1) is broadly expressed in steroid-sensitive brain areas that control the expression of male copulatory behavior, and we investigated the role of this coactivator by antisense technology. Daily intracerebroventricular injections of locked nucleic acid (LNA) antisense (AS) oligonucleotides targeting SRC-1 significantly reduced the expression of androgen- and estrogen-dependent male-typical sexual behaviors compared with control animals that received the vehicle alone or scrambled oligonucleotides. Sexual behavior was restored and even enhanced within 48 h after interruption of LNA injections. Western blot analysis confirmed the decrease of SRC-1 expression in AS animals and suggested an overexpression 48 h after the end of injections. The effects of SRC-1 knock-down on behavior correlated with a reduction in volume of the preoptic medial nucleus (POM) when its borders were defined by Nissl staining or by aromatase immunohistochemistry. The amount of aromatase-immunoreactive material in POM was also reduced in the AS compared with the control group. Previous work on SRC-1 knock-out mice raised questions about the importance of this specific coactivator in the regulation of reproductive behavior and development of sexually dimorphic structures in the CNS. Together, the present findings indicate that SRC-1 modulates steroid-dependent gene transcription and behavior and highlight the rapid time course of steroid-induced brain plasticity in adult quail.
Disciplines :
Neurosciences & behavior
Author, co-author :
Charlier, Thierry ;  Université de Liège - ULiège > Département des sciences biomédicales et précliniques > Biologie de la différenciation sexuelle du cerveau
Ball, Gregory F
Balthazart, Jacques  ;  Université de Liège - ULiège > Département des sciences biomédicales et précliniques > Biologie de la différenciation sexuelle du cerveau
Language :
English
Title :
Inhibition of steroid receptor coactivator-1 blocks estrogen and androgen action on male sex behavior and associated brain plasticity.
Publication date :
2005
Journal title :
Journal of Neuroscience
ISSN :
0270-6474
eISSN :
1529-2401
Publisher :
Society for Neuroscience, Washington, United States - District of Columbia
Volume :
25
Issue :
4
Pages :
906-13
Peer reviewed :
Peer Reviewed verified by ORBi
Available on ORBi :
since 20 April 2009

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