Role of leukotriene C4 in follicle-stimulating hormone (FSH) secretion in female rat pituitary

Gynecol Endocrinol. 1996 Apr;10(2):95-100. doi: 10.3109/09513599609097898.

Abstract

Leukotriene C4, at doses of 0.01 and 0.1 nmol/l added to superfused cells in pulse of 4-min duration, evoked follicle-stimulating hormone (FSH) release up to 12- to 26-fold of basal secretion. Higher and lower concentrations of leukotriene C4 were not able to induce FSH secretion. Gonadotropin-releasing hormone (GnRH)-induced FSH release was reduced by 38-57% by the leukotriene receptor antagonist FPL 55712 (10 mumol/l). Moreover, we have shown that FSH release occurs parallel to leukotriene C4 synthesis in rat anterior pituitary cells. Mellitin (100 nmol/l), an activator of phospholipase A2, induced FSH and radioactivity secretion in rat anterior pituitary cells previously preincubated for 24 h with [3H]arachidonic acid (AA).

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cells, Cultured
  • Chromones / pharmacology
  • Female
  • Follicle Stimulating Hormone / biosynthesis
  • Follicle Stimulating Hormone / metabolism*
  • Gonadotropin-Releasing Hormone / pharmacology
  • Leukotriene C4 / biosynthesis
  • Leukotriene C4 / physiology*
  • Lipoxygenase Inhibitors / pharmacology
  • Melitten / pharmacology
  • Pituitary Gland, Anterior / cytology
  • Pituitary Gland, Anterior / drug effects
  • Pituitary Gland, Anterior / metabolism*
  • Radioimmunoassay
  • Rats
  • Rats, Sprague-Dawley

Substances

  • Chromones
  • Lipoxygenase Inhibitors
  • Melitten
  • Leukotriene C4
  • Gonadotropin-Releasing Hormone
  • FPL 55712
  • Follicle Stimulating Hormone