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硫酸阿托品可调节雌性而非雄性大鼠下丘脑的雌激素结合。

Atropine sulfate modulates estrogen binding by female, but not male, rat hypothalamus.

作者信息

Lauber A H

机构信息

Department of Psychology, University of California, Riverside 92521.

出版信息

Brain Res Bull. 1988 Feb;20(2):273-6. doi: 10.1016/0361-9230(88)90190-6.

Abstract

Studies have shown that pharmacological manipulation of the dopamine, norepinephrine and muscarinic cholinergic neurotransmitter systems modulates the number of neural estrogen binding sites. Previously, we reported that the muscarinic agonist, bethanechol, increased estrogen receptor binding by hypothalamic cytosols from female, but not male, rats. Moreover, pretreatment with atropine prevented the bethanechol-induced effect. The experiments reported here were executed with the expectation that atropine alone would either decrease or fail to alter estrogen binding. However, the present data show that atropine increases estrogen binding by female, but not male, hypothalamic cytosols. Thus, it appears that a muscarinic antagonist and agonist can similarly affect the concentration of estrogen binding sites in female rat hypothalamus.

摘要

研究表明,对多巴胺、去甲肾上腺素和毒蕈碱型胆碱能神经递质系统进行药理操作可调节神经雌激素结合位点的数量。此前,我们报道毒蕈碱激动剂氯贝胆碱可增加雌性而非雄性大鼠下丘脑胞质溶胶中的雌激素受体结合。此外,用阿托品预处理可防止氯贝胆碱诱导的效应。进行此处报道的实验时预期单独使用阿托品会降低或不改变雌激素结合。然而,目前的数据表明,阿托品可增加雌性而非雄性大鼠下丘脑胞质溶胶中的雌激素结合。因此,似乎毒蕈碱拮抗剂和激动剂可类似地影响雌性大鼠下丘脑雌激素结合位点的浓度。

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