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This Article Full Text Full Text (PDF) A corrigendum has been published All Versions of this Article: 296/6/E1409    most recent 00037.2009v1 Alert me when this article is cited Alert me if a correction is posted Citation Map Services Email this article to a friend Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal Download to citation manager Google Scholar Articles by Pak, T. R. Articles by Handa, R. J. PubMed PubMed Citation Articles by Pak, T. R. Articles by Handa, R. J.

Arginine vasopressin regulation in pre- and postpubertal male rats by the androgen metabolite 3β-diol

¹Department of Cell Biology, Neurobiology, and Anatomy, Loyola University Chicago Stritch School of Medicine, Maywood, Illinois; ²Department of Integrative Physiology, University of Colorado, Boulder, Colorado; and ³Department of Basic Medical Sciences, University of Arizona, College of Medicine, Phoenix, Arizona

Submitted 15 January 2009 ; accepted in final form 17 April 2009

Arginine vasopressin (AVP) is a nonapeptide expressed in several brain regions. In addition to its well-characterized role in osmoregulation, AVP regulates paternal behavior, aggression, circadian rhythms, and the stress response. In the bed nucleus of the stria terminalis (BST), AVP gene expression is tightly regulated by gonadal steroid hormones. However, the degree by which AVP is regulated by gonadal steroid hormones in the suprachiasmatic nucleus (SCN) and medial amygdala (MeA) is unclear. Previous studies have shown that AVP expression in the brain of gonadectomized rats is restored with testosterone, 17β-estradiol, and 5-dihydrotestosterone (DHT) replacement. In addition, we have demonstrated that 3β-diol, a metabolite of DHT, increased AVP promoter activity in a neuronal cell line and that the effects of 3β-diol on AVP promoter activity were mediated by estrogen receptor-β. To test whether 3β-diol has a physiological role in the regulation of central AVP expression in vivo, we gonadectomized pre- and postpubertal male rats and followed with once daily injections of estradiol benzoate (EB), DHT-propionate, 3β-diol-dipropionate, or vehicle. The SCN, BST, and MeA were analyzed for AVP mRNA expression using in situ hybridization. In the BST, intact juveniles had significantly fewer AVP-expressing cells than adults. GDX abolished all AVP mRNA expression in the BST in both age groups, whereas treatment with EB restored >80% and DHTP <10% of the AVP expression. Interestingly, 3β-diol-proprionate was more effective at inducing AVP expression in juveniles than in adults, suggesting that the regulation of AVP by 3β-diol might be age dependent.

5-androstane-3β,17β-diol