垂体腺苷酸环化酶激活多肽38 (pacap38)对雄性大鼠体内促黄体生成素(LH)分泌的影响。

Y Osuga, N Mitsuhashi, M Mizuno
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引用次数: 61

摘要

鉴于最近的研究表明垂体腺苷酸环化酶激活多肽(PACAP) 38刺激垂体多余细胞释放LH,并且下丘脑和垂体前叶对该肽具有高度选择性的结合位点,我们研究了心房内注射PACAP 38和血管活性肠肽(VIP)的效果,后者与PACAP 38具有68%的同源性。进一步观察pacap38在脑室内注射的作用。心房内(10、30、100微克)和体外(8、32微克)给予PACAP 38显著刺激黄体生成素释放(P < 0.01),呈剂量相关。注射0.8微克的Icv无效。房内注射与体外注射促黄体生成素释放的时间规律相似,但房内注射促黄体生成素的升高幅度明显高于体外注射促黄体生成素。房内给药VIP对LH释放几乎没有影响。这些结果表明pacap38能促进体内LH的释放。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
In vivo effect of pituitary adenylate cyclase activating polypeptide 38 (PACAP 38) on the secretion of luteinizing hormone (LH) in male rats.

In view of the recent demonstrations that pituitary adenylate cyclase activating polypeptide (PACAP) 38 stimulates the release of LH from superfused pituitary cells and that the hypothalamus and anterior pituitary have highly selective binding sites for the peptide, we have surveyed the effect of intraatrial injections of PACAP 38 and vasoactive intestinal peptide (VIP), which has 68% homology with PACAP 38, in intact adult male rats. Furthermore the effect of intracerebroventricular (icv) injection of PACAP 38 was investigated. Intraatrial (10, 30, 100 micrograms) and icv (8, 32 micrograms) administration of PACAP 38 stimulated LH release significantly (P less than 0.01) in a dose-related fashion. Icv injection at a dose of 0.8 microgram was ineffective. The time course pattern of LH release by intraatrial injection and that by icv injection was similar, but the LH levels increased by intraatrial injection were much higher than that by icv injection. Intraatrial administration of VIP had almost no effect on LH release. These findings suggested that PACAP 38 stimulates LH release in vivo.

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