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脑室注射促性腺激素释放激素或β-内啡肽对雌性大鼠促黄体生成素亚基基因表达的调节作用

Modulation of luteinizing hormone subunit gene expression by intracerebroventricular microinjection of gonadotropin-releasing hormone or beta-endorphin in female rats.

作者信息

Gajewska A, Kochman K, Lerrant Y, Kochman H, Counis R

机构信息

Kielanowski Institute of Animal Physiology and Nutrition, Jablonna near Warsaw, Poland.

出版信息

Biochim Biophys Acta. 2000 Oct 18;1523(2-3):217-24. doi: 10.1016/s0304-4165(00)00125-2.

Abstract

The effects of gonadotropin-releasing hormone (GnRH), beta-endorphin and its antagonist naloxone on the expression of luteinizing hormone (LH) subunit genes and LH secretion were examined in ovariectomized and/or cycling female rats through their direct microinjection into the third cerebral ventricle, in the proximity of the hypothalamus-pituitary complex. GnRH (1 nM) induced a significant augmentation of the pituitary content of alpha mRNA when administered 15, 30 or 60 min intervals over 5 h to ovariectomized rats whereas only the 30 and 60 min intervals were effective in increasing LHbeta mRNA, and the 60 min intervals for LH release. This was in agreement with the established concept of a pulse-dependent regulation of gonadotropin synthesis and release. Hourly pulses of GnRH also increased alpha and LHbeta mRNA levels when microinjected in female cycling rats during proestrus or diestrus II. Using this model we observed a marked negative influence of hourly intracerebral microinjections of beta-endorphin on LH mRNA content and LH release in ovariectomized rats while naloxone had no effect. This suggests that endogenous beta-endorphin was unable to exert its negative action on beta-endorphin receptors that were present and responded to the ligand. The present approach would be valuable for the exploration of the mechanisms of action of beta-endorphin or other substances on the functions of the gonadotrophs.

摘要

通过将促性腺激素释放激素(GnRH)、β-内啡肽及其拮抗剂纳洛酮直接微量注射到第三脑室(靠近下丘脑-垂体复合体),研究了它们对去卵巢和/或处于发情周期的雌性大鼠促黄体生成素(LH)亚基基因表达和LH分泌的影响。给去卵巢大鼠在5小时内每隔15、30或60分钟注射一次GnRH(1 nM),可显著增加垂体中α mRNA的含量,而只有30分钟和60分钟的间隔能有效增加LHβ mRNA,60分钟的间隔能促进LH释放。这与促性腺激素合成和释放的脉冲依赖性调节这一既定概念相符。在发情前期或动情周期II期给处于发情周期的雌性大鼠微量注射GnRH,每小时一次的脉冲也会增加α和LHβ mRNA水平。利用该模型,我们观察到每小时向去卵巢大鼠脑内微量注射β-内啡肽对LH mRNA含量和LH释放有显著负面影响,而纳洛酮则无作用。这表明内源性β-内啡肽无法对存在且能对配体作出反应的β-内啡肽受体发挥其负面作用。本方法对于探索β-内啡肽或其他物质对促性腺细胞功能的作用机制具有重要价值。

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