This study investigated the hypothesis that for a subpopulation of horse mares continuation of estrous cycles during the nonbreeding season may be attributed to continued stimulatory glutamatergic activity on GnRH-secreting neurons. The gonadotropin response to the glutamatergic agonist N-methyl-DL-aspartic acid (NMA) was compared in cycling and anestrous mares during the nonbreeding season. It was anticipated that the gonadotropin response to NMA in cycling mares would be attenuated, compared with that of anestrous mares. The experiment used 16 anestrous mares and 15 mares that cycled during the nonbreeding season. The effect of NMA on prolactin secretion was also evaluated. In addition, the seasonal rhythm of prolactin secretion was compared in anestrous and cycling mares during October-April. In cycling mares, the response to NMA was dependent on the stage of the cycle, and a significantly (p < 0.05) larger proportion responded during the luteal phase (6 of 8), compared with the follicular phase (1 of 7 mares). The proportion of anestrous mares that responded to NMA was similar to that of cycling mares during the luteal phase, but larger than during the follicular phase. In anestrous and cycling mares, NMA suppressed prolactin secretion, and in both groups prolactin secretion decreased during the nonbreeding season. Thus, we conclude that differences in reproductive activity in mares during the nonbreeding season are unlikely to reflect a change in glutamatergic activity.
In the mare, endogenous opioids have been implicated in the suppression of gonadotropin secretion during seasonal anestrus (AN). The present study tested whether continuation of reproductive activity during the nonbreeding season (NBS) reflects the absence of a seasonal shift in opioid tone compared to what occurs in AN mares. During the NBS, 11 AN and 8 luteal-phase mares received 0.1, 0.05, 0. 025 mg/kg naloxone (NAL) or vehicle on alternate days. Whereas cycling mares responded to all dosages of NAL, AN mares responded only to the higher dosages for FSH, and LH failed to increase at any dosage employed. During the breeding season (BS), the response to these dosages of NAL was reevaluated in 12 mares in the luteal phase of a synchronized estrous cycle. Although there was no difference between cycling mares during the breeding and nonbreeding seasons in FSH response, those mares that had cycled during the NBS showed a greater LH response to 0.05 mg/kg NAL than mares during the BS. From these data, we conclude that opioid tone is lower during the BS than during AN and that this shift in inhibitory tone does not occur in mares that cycle during the NBS. Thus, reduced opioid tone may play a role in the mechanisms controlling the nonseasonal exhibition of estrous cycles in the mare.
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