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钙离子激活的钾通道参与垂体催乳素分泌调节的证据。

Evidence that Ca(2+)-activated K+ channels participate in the regulation of pituitary prolactin secretion.

作者信息

Wang X, Inukai T, Greer M A, Greer S E

机构信息

Department of Physiology, Oregon Health Sciences University, Portland 97201.

出版信息

Brain Res. 1994 Oct 31;662(1-2):83-7. doi: 10.1016/0006-8993(94)90798-6.

Abstract

We evaluated the role of Ca(2+)-activated K+ channels in the regulation of prolactin (PRL) secretion with a perifusion system using acutely dispersed rat anterior pituitary cells. Apamin, which blocks Ca(2+)-activated K+ channels, induced PRL secretion in a dose-dependent fashion between 1 and 300 nM (r = 0.99, P < 0.01). Charybdotoxin, another Ca(2+)-activated K+ channel-blocker, also induced PRL secretion at 20 nM concentration. These were not non-specific toxic effects, since stimulation of PRL secretion by 10 nM thyrotropin-releasing hormone (TRH) was not different before and after applying the channel-blockers. Both 10 microM dopamine and 2 microM nifedipine significantly, but incompletely, depressed PRL secretion induced by 100 nM apamin; 10 microM dopamine completely blocked PRL secretion induced by 20 nM charybdotoxin. Our data indicate that Ca(2+)-activated K+ channels may play an important role in the regulation of PRL secretion.

摘要

我们使用急性分离的大鼠垂体前叶细胞的灌流系统,评估了钙激活钾通道在催乳素(PRL)分泌调节中的作用。蜂毒明肽可阻断钙激活钾通道,在1至300 nM之间以剂量依赖方式诱导PRL分泌(r = 0.99,P < 0.01)。另一种钙激活钾通道阻滞剂蝎毒素,在20 nM浓度时也可诱导PRL分泌。这些并非非特异性毒性作用,因为在应用通道阻滞剂前后,10 nM促甲状腺激素释放激素(TRH)对PRL分泌的刺激并无差异。10 μM多巴胺和2 μM硝苯地平均显著但不完全抑制100 nM蜂毒明肽诱导的PRL分泌;10 μM多巴胺完全阻断20 nM蝎毒素诱导的PRL分泌。我们的数据表明,钙激活钾通道可能在PRL分泌调节中起重要作用。

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