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血清素对体外培养的大鼠垂体促黄体生成素基础释放及促性腺激素释放激素诱导释放的影响。

Effect of serotonin on the basal and gonadotrophin-releasing hormone-induced release of luteinizing hormone from rat pituitary glands in vitro.

作者信息

Apfelbaum M E

机构信息

Instituto de Investigación Médica Mercedes y Martín Ferreyra, Córdoba, Argentina.

出版信息

Life Sci. 1987 Oct 26;41(17):2069-76. doi: 10.1016/0024-3205(87)90482-6.

DOI:10.1016/0024-3205(87)90482-6
PMID:3312904
Abstract

The effect of serotonin (5-HT) on the basal and gonadotrophin-releasing hormone (GnRH)-stimulated release of luteinizing hormone (LH) was studied in rat adenohypophysis in vitro. Anterior pituitary glands from ovariectomized rats were incubated for 1h in the presence of different doses of 5-HT (0.01 to 3 mumol/l). Serotonin added to the culture medium slightly dimished the basal release of LH and markedly inhibited the release of LH induced by GnRH. Responsiveness to GnRH (3 nmol/l) was significantly reduced, in a dose-dependent manner, by the simultaneous treatment of glands with 5-HT. Maximal inhibition to 65% of the response obtained with GnRH alone, was attained with 1 mumol/l 5-HT. The EC50 value was estimated to be about 1.9 X 10(-7) M. The inhibitory effect of 5-HT was evident within 30 min of incubation. Furthermore, 5-HT appear to exert a short-lasting action, since the rate of basal and GnRH-induced release of LH was reduced during the first hour of incubation, but after 2h the suppressive effects of 5-HT were no longer apparent. Methysergide, a serotonin receptor blocking agent, partially antagonized the inhibitory effect of 5-HT on LH release, either basal or GnRH-stimulated. This suggests that a receptor-mediated component may be involved in the mechanism of 5-HT action. The present results indicate that 5-HT can affect the release of LH by acting directly at the pituitary gland level.

摘要

在体外对大鼠腺垂体进行研究,观察血清素(5-羟色胺,5-HT)对基础状态下及促性腺激素释放激素(GnRH)刺激的促黄体生成素(LH)释放的影响。将去卵巢大鼠的垂体前叶在不同剂量的5-HT(0.01至3μmol/L)存在下孵育1小时。添加到培养基中的血清素略微减少了LH的基础释放,并显著抑制了GnRH诱导的LH释放。同时用5-HT处理腺垂体,对GnRH(3nmol/L)的反应性以剂量依赖方式显著降低。用1μmol/L的5-HT可达到对单独使用GnRH时获得的反应的最大抑制,即抑制至65%。估计半数有效浓度(EC50)值约为1.9×10⁻⁷M。5-HT的抑制作用在孵育30分钟内即可显现。此外,5-HT似乎发挥的是短暂作用,因为在孵育的第一个小时内,基础状态下及GnRH诱导的LH释放速率均降低,但2小时后5-HT的抑制作用不再明显。血清素受体阻断剂麦角新碱部分拮抗了5-HT对基础或GnRH刺激的LH释放的抑制作用。这表明受体介导的成分可能参与了5-HT的作用机制。目前的结果表明,5-HT可通过直接作用于垂体水平来影响LH的释放。

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