Stimulatory effect of PYY-(3-36) on gonadotropin secretion is potentiated in fasted rats

Am J Physiol Endocrinol Metab. 2006 Jun;290(6):E1162-71. doi: 10.1152/ajpendo.00469.2005. Epub 2006 Jan 3.

Abstract

Development and normal function of the reproductive axis requires a precise degree of body energy stores. Polypeptide YY-(3-36) [PYY-(3-36)] is a gastrointestinal secreted molecule recently shown to be involved in the control of food intake with agonistic activity on neuropeptide Y (NPY) receptor subtypes Y2 and Y5. Notably, PYY-(3-36) has been recently demonstrated as putative regulator of gonadotropin secretion in the rat. However, the "reproductive" facet of this factor remains to be fully elucidated. In this context, we report herein our analyses of the influence of the nutritional status on the effects of PYY-(3-36) upon GnRH and gonadotropin secretion. The major findings of our study are 1) the stimulatory effect of central administration of PYY-(3-36) on LH secretion was significantly enhanced after fasting and blocked by a GnRH antagonist; 2) besides central effects, PYY-(3-36) elicited LH and FSH secretion directly at the pituitary level, a response that is also augmented by fasting; 3) PYY-(3-36) inhibited GnRH secretion by hypothalamic fragments from male rats fed ad libitum, whereas a significant stimulatory effect was observed after fasting; and 4) the increase in the gonadotropin responsiveness to PYY-(3-36) in fasting was not associated with changes in the expression of Y2 and Y5 receptor genes at hypothalamus and/or pituitary. In conclusion, our study extends our previous observations suggesting a relevant, mostly stimulatory, role of PYY-(3-36) in the control of gonadotropin secretion. Strikingly, such an effect was significantly enhanced by fasting. Considering the proposed decrease in PYY-(3-36) levels after fasting, the possibility that reduced PYY-(3-36) secretion might contribute to defective function of the gonadotropic axis after food deprivation merits further investigation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Eating
  • Fasting / physiology*
  • Female
  • Follicle Stimulating Hormone / metabolism
  • Gonadotropin-Releasing Hormone / metabolism
  • Gonadotropins / blood
  • Gonadotropins / metabolism*
  • Hypothalamus / metabolism
  • In Vitro Techniques
  • Luteinizing Hormone / metabolism
  • Male
  • Peptide YY / pharmacology*
  • Pituitary Gland / metabolism*
  • Rats
  • Rats, Wistar

Substances

  • Gonadotropins
  • Peptide YY
  • Gonadotropin-Releasing Hormone
  • Luteinizing Hormone
  • Follicle Stimulating Hormone