AJP - Endo AJP: Renal Physiology
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Am J Physiol Endocrinol Metab 293: E1385-E1392, 2007. First published September 4, 2007; doi:10.1152/ajpendo.00274.2007
0193-1849/07 $8.00
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
293/5/E1385    most recent
00274.2007v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Pinilla, L.
Right arrow Articles by Aguilar, E.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Pinilla, L.
Right arrow Articles by Aguilar, E.

Selective role of neuropeptide Y receptor subtype Y2 in the control of gonadotropin secretion in the rat

L. Pinilla,* R. Fernández-Fernández,* J. Roa, J. M. Castellano, M. Tena-Sempere, and E. Aguilar

Department of Cell Biology, Physiology, and Immunology, University of Córdoba, Córdoba; and Centro de Investigación Biomédica en Red (CB06/03) Fisiopatología de la Obesidad y Nutrición, Instituto Salud Carlos III, Madrid, Spain

Submitted 2 May 2007 ; accepted in final form 31 August 2007

Different signals with key roles in energy homeostasis regulate the reproductive axis. These include neuropeptide Y and polypeptide YY3-36, whose type Y2 receptor is the most abundant of this family in the brain. We evaluated herein the putative roles of Y2 receptors in the control of gonadotropin secretion by means of central administration of PYY13-36 (agonist of Y2 receptors) and BIIE 0246 (antagonist of Y2 receptors) to intact and orchidectomized male rats. In addition, the ability of PYY13-36 to elicit GnRH and gonadotropin secretion in vitro and the impact of fasting on LH responses to PYY13-36 in vivo were also monitored. Central administration of PYY13-36 significantly decreased the circulating levels of both gonadotropins, an effect that was observed in prepubertal and adult rats. Yet a dual action of Y2 receptors in the control of male gonadotropic axis was evidenced as their activation induced 1) stimulation of gonadotropin responses to GnRH at the pituitary but 2) inhibition of GnRH secretion at the hypothalamus. Antagonization of Y2 receptors failed to modify basal LH secretion in intact males either after being fed ad libitum or after being fasted. In contrast, their central blockade in orchidectomized rats evoked a significant increase in circulating LH and FSH level, suggesting the constitutive activation of Y2 receptor in such stimulated conditions. In summary, our data evidence a complex mode of action of Y2 receptors in the control of gonadotropic axis, with stimulatory and inhibitory actions at different levels of the system that are sensitive to the gonadal status.

polypeptide YY3-36; luteinizing hormone-releasing hormone; luteinizing hormone; follicle-stimulating hormone; fasting; pituitary



Address for reprint requests and other correspondence: E. Aguilar, Physiology Section, Dept. of Cell Biology, Physiology, and Immunology, Faculty of Medicine, Univ. of Córdoba, Avda. Menéndez Pidal s/n, 14004 Córdoba, Spain (e-mail: fi1agbee{at}uco.es)







HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Visit Other APS Journals Online
Copyright © 2007 by the American Physiological Society.