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在关键期,视前区的毒蕈碱受体对17β-雌二醇敏感。

Muscarinic receptors in the preoptic area are sensitive to 17 beta-estradiol during the critical period.

作者信息

Egozi Y, Kloog Y

出版信息

Neuroendocrinology. 1985 May;40(5):385-92. doi: 10.1159/000124103.

Abstract

The relationship between the steroid hormone 17 beta-estradiol and the muscarinic cholinergic receptors present in the preoptic area (POA), median hypothalamus and posterior hypothalamus of female rats was examined in vitro at various stages of the estrous cycle. Muscarinic receptors varied in a cyclic manner, specifically in the POA, as shown by an increase in the proportion of high-affinity agonist binding sites (RH) to 60% during the proestrus, as compared to RH proportion observed during diestrus-2 and during the afternoon of proestrus (35%). Exposure of POA homogenates to 17 beta-estradiol resulted in conversion of RH to low-affinity agonist binding sites (RL). This effect of the hormone was also restricted to the POA taken from rats during the morning of proestrus. It was blocked by the antiestrogenic drug, clomiphene, and could be prevented by preoccupation of the muscarinic receptors by their own ligands prior to the addition of hormone. It follows that significant changes in POA muscarinic receptors in situ exactly coincided with the known critical time period characterized by high estrogen levels and high levels of estrogen receptors in the POA. These changes in muscarinic receptors might thus conceivably reflect variations in cholinergic activity in the POA during the estrous cycle.

摘要

在雌性大鼠发情周期的不同阶段,在体外研究了甾体激素17β - 雌二醇与存在于视前区(POA)、下丘脑中部和下丘脑后部的毒蕈碱胆碱能受体之间的关系。毒蕈碱受体呈周期性变化,特别是在视前区,如在发情前期,高亲和力激动剂结合位点(RH)的比例增加到60%,而在间情期-2和发情前期下午观察到的RH比例为35%。将视前区匀浆暴露于17β - 雌二醇导致RH转化为低亲和力激动剂结合位点(RL)。激素的这种作用也仅限于取自发情前期上午大鼠的视前区。它被抗雌激素药物克罗米芬阻断,并且在添加激素之前,通过其自身配体预先占据毒蕈碱受体可以预防这种作用。由此可见,视前区毒蕈碱受体的显著变化与已知的以视前区高雌激素水平和高雌激素受体水平为特征的关键时期恰好吻合。因此,毒蕈碱受体的这些变化可能反映了发情周期中视前区胆碱能活性的变化。

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