The present study w a s undertaken to determine the effects of the endogenous opioid ligand 1-endorphin on pulsatile luteinizing hormone (LH) secretion and plasma prolactin concentrations during the follicular phase of the ewe. Oestrous cycles were synchronized by injection of prostaglandin analogue and, commencing 13 h later, saline or 1-endorphin (2, 10 or 50pg) was irilected intracerebroventricularly at hourly intervals for 3 h. Treatment with /%endorphin was followed by a significant reduction iii LH pulse frequency at all doses due to almost complete cessation of pulses. There were no significant changes in LH pulse amplitude or mean LH concentrations. At the lowest dose of ,&endorphin, LH pulses recommenced within 3 h of the last injection if; all animals and pulse frequency was not significantly different from the saline-injected controls during the 3 h post-treatment pcriod. Following treatment with 10 or 50 pg j-endorphin, LH pulse frequency remained suppressed during the 3 h post-treatment pt.riod but was not different from saline-treated controls on the following day. The time to the onset of the LH surge w a s not affected by intracerebroventricular j-endorphin. Plasma prolactin concentrations were significantly increased following intracerebroventricular injection of 10 or 50 pg 1-endorphin, declining to control values soon after treatments stopped. Intravenous administration of 50 pg j-endorphin had no effect on LH but w a s accompanied by a small increase in prolactin concentrations.While these results indicate that hypothalamic 8-endorphin may be involved in the central control of LH and prolactin secretion, they provide no evidence for subtle modulation of LH pulse frequency by this neuropeptide.St d i e s from a number of species have clearly demonstrated that tiic endogenous opioid peptides are potent inhibitors of luteinizing h>ii.mone (LH) secretion (1-3). However, much less is known ;I!)irut their role as physiological modulators of reproductive lu::iction. During the follicular phase of the oestrous cycle, subtle c!i.inges in LH pulse frequency and amplitude are likely to affect gi-owth and maturation of ovarian follicles which could be risllccted in parameters such as the ovulation rate. Opioid agonists ii id antagonists suppress and enhance follicular phase LH secre-[ i i u i , respectively (I), but there is little information on the effects 01 endogenous ligands such as 8-endorphin on pulsatile LH sccretion.The endogenous opioid peptides have also been implicated in the. control of prolactin secretion. Opioid agonists clearly stimu-1~1~ prolactin secretion in the rat (3); however in sheep, although nlorphine stimulates prolactin secretion (4), the mixed mu-and kappa-receptor agonist FD 33-824 has no effect suggesting that Prolactin secretion may be under different opioid control (5).The present study was undertaken to provide information on I h possible role of the endogenous opioid ligand j-endorphin in modulation of LH and prolactin secretion during the follicular phase. In p...