Correlation of hypothalamic somatostatin mRNA expression and peptide content with secretion: Sexual dimorphism and differential regulation by gonadalfactors

Citation
He. Murray et al., Correlation of hypothalamic somatostatin mRNA expression and peptide content with secretion: Sexual dimorphism and differential regulation by gonadalfactors, J NEUROENDO, 11(1), 1999, pp. 27-33
Citations number
33
Categorie Soggetti
Neurosciences & Behavoir
Journal title
JOURNAL OF NEUROENDOCRINOLOGY
ISSN journal
09538194 → ACNP
Volume
11
Issue
1
Year of publication
1999
Pages
27 - 33
Database
ISI
SICI code
0953-8194(199901)11:1<27:COHSME>2.0.ZU;2-J
Abstract
Sex differences in growth hormone (GH) secretion in the rat are thought to be determined, to a large extent, by gonadal steroid-dependent sex differen ces in somatostatin (SRIH) secretion from neurones in the periventricular n ucleus (PeN) which project to the median eminence (ME). The present study a imed to obtain direct evidence for sex differences and gonadal regulation o f SRIH release within this pathway and to determine the relationships betwe en SRIH mRNA expression, SRIH peptide content and SRIH secretion in the adu lt rat. Somatostatin mRNA expression in the PeN and peptide content in both PeN and ME were higher in males than females (P<0.05). However, both basal and 56 mM K+-stimulated SRIH release in vitro from hypothalamic explants i ncorporating the PeN-ME pathway were higher (P<0.01) in females. The gonade ctomy of female rats resulted in significantly reduced basal levels of SRIH release equivalent to that of males but had no effect on SRIH mRNA/peptide content or K+-stimulated release. In contrast, gonadectomy of male rats re duced SRIH mRNA and peptide contents and elevated K+-stimulated secretion ( P<0.01) to levels similar to that seen in intact females, without affecting basal release. In summary, these results demonstrate that in the PeN-ME of the adult rat: (1) SRIH mRNA and peptide content is well correlated and se xually dimorphic but dependent on gonadal factors in the male only; (2) SRI H secretion is sexually dimorphic and dependent on gonadal factors; but (3) differences in mRNA/peptide content do not reflect secretory capacity; and (4) gonadal factors differentially modulate SRIH secretory dynamics in mal es and females.