Reid R L, Quigley M E, Yen S S
J Clin Endocrinol Metab. 1983 Dec;57(6):1107-10. doi: 10.1210/jcem-57-6-1107.
In postmenopausal women, the administration of beta-endorphin in repeated pulses (1-2.5 mg) at 1- to 2-h intervals or constant infusion (1 mg/h) for 3-6 h elicited the prompt release of PRL without concomitant change in LH levels. Infusion of an opiate receptor antagonist, naloxone (1.6 mg/h), for 6-7 h also had no effect on LH levels. Since substantial evidence indicates that endogneous opioid peptides exert an inhibitory role on GnRH-LH secretion and that the functional activity of opiate receptors appears to be ovarian steroid dependent, the present observation suggests that the hypersecretion of gonadotropin in the absence of ovarian steroid feedback may, in part, be causally related to a reduced opioid inhibition of GnRH-LH release.
在绝经后女性中,以1至2小时的间隔重复脉冲式给予β-内啡肽(1 - 2.5毫克)或持续输注(1毫克/小时)3至6小时,可促使催乳素迅速释放,而促黄体生成素(LH)水平无相应变化。输注阿片受体拮抗剂纳洛酮(1.6毫克/小时)6至7小时对LH水平也无影响。由于大量证据表明内源性阿片肽对促性腺激素释放激素(GnRH)-LH分泌发挥抑制作用,且阿片受体的功能活性似乎依赖于卵巢甾体激素,目前的观察结果提示,在缺乏卵巢甾体激素反馈的情况下促性腺激素分泌过多可能部分与阿片类物质对GnRH-LH释放的抑制作用减弱存在因果关系。