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内源性阿片肽对人胎儿下丘脑促性腺激素释放激素体外释放的调节

Endogenous opioid regulation of gonadotropin-releasing hormone release from the human fetal hypothalamus in vitro.

作者信息

Rasmussen D D, Liu J H, Wolf P L, Yen S S

出版信息

J Clin Endocrinol Metab. 1983 Nov;57(5):881-4. doi: 10.1210/jcem-57-5-881.

Abstract

Endogenous opioid regulation of GnRH release from the human fetal (21-23 weeks gestation) mediobasal hypothalamus was investigated in an in vitro perifusion system. Pulse injection of an opiate receptor antagonist, naloxone, reproducibly elicited an acute increase in GnRH release within 30 min. Constant infusion of naloxone (60 min) induced a sustained increase in GnRH release, which was promptly inhibited by a pulse of beta-endorphin administered halfway during the naloxone infusion. These studies unequivocally demonstrate that endogenous opiates exert an inhibitory effect on GnRH release from the human fetal mediobasal hypothalamus in vitro.

摘要

利用体外灌流系统研究了内源性阿片类物质对人胎儿(妊娠21 - 23周)中基底下丘脑促性腺激素释放激素(GnRH)释放的调节作用。脉冲注射阿片受体拮抗剂纳洛酮,可在30分钟内重复性地引起GnRH释放急性增加。持续输注纳洛酮(60分钟)可诱导GnRH释放持续增加,在纳洛酮输注过程中间给予一次β-内啡肽脉冲可迅速抑制这种增加。这些研究明确表明,内源性阿片类物质在体外对人胎儿中基底下丘脑的GnRH释放发挥抑制作用。

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