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培养的神经胶质细胞上的α和β肾上腺素能受体。

Alpha- and beta-adrenoceptors on cultured glial cells.

作者信息

Hösli L, Hösli E, Zehntner C, Lehmann R, Lutz T W

出版信息

Adv Biochem Psychopharmacol. 1983;37:417-20.

PMID:6314767
Abstract

The action of alpha- and beta-adrenoceptor agonists and antagonists has been studied on the membrane potential of glial cells in cultured rat central nervous system. Noradrenaline and the alpha-agonist phenylephrine caused a depolarization which was reversibly blocked by the alpha-antagonist phentolamine. In contrast, the beta-agonist isoprenaline hyperpolarized the glial membrane. This hyperpolarization was not associated with measurable changes in membrane resistance and was antagonized by the beta-blocker atenolol. These results suggest that the glial depolarization is mediated by activation of alpha-receptors, whereas the hyperpolarization is due to stimulation of beta-receptors. The existence of alpha- and beta-adrenoceptors on glial cells is further supported by autoradiographic studies showing binding of noradrenaline and alpha- and beta-antagonists to astrocytes.

摘要

已对α-和β-肾上腺素能受体激动剂及拮抗剂对培养的大鼠中枢神经系统胶质细胞膜电位的作用进行了研究。去甲肾上腺素和α-激动剂去氧肾上腺素引起去极化,该去极化被α-拮抗剂酚妥拉明可逆性阻断。相比之下,β-激动剂异丙肾上腺素使胶质细胞膜超极化。这种超极化与膜电阻的可测量变化无关,并被β-阻滞剂阿替洛尔拮抗。这些结果表明,胶质细胞去极化是由α-受体激活介导的,而超极化是由于β-受体刺激所致。放射自显影研究显示去甲肾上腺素以及α-和β-拮抗剂与星形胶质细胞结合,进一步支持了胶质细胞上存在α-和β-肾上腺素能受体。

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