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含有GIRK2亚基的G蛋白门控钾通道(GIRK)是药理学诱导低温反应的控制枢纽。

G-protein-gated potassium (GIRK) channels containing the GIRK2 subunit are control hubs for pharmacologically induced hypothermic responses.

作者信息

Costa Alberto C S, Stasko Melissa R, Stoffel Markus, Scott-McKean Jonah J

机构信息

Eleanor Roosevelt Institute, University of Denver, Denver, Colorado 80206, USA.

出版信息

J Neurosci. 2005 Aug 24;25(34):7801-4. doi: 10.1523/JNEUROSCI.1699-05.2005.

Abstract

Hypothermic responses of rodents to the peripheral or intraventricular injection of many individual neurotransmitter receptor agonists have been well documented. Because many hypothermia-inducing agonists are also known to activate G-protein-gated potassium (GIRK) channels, we investigated the hypothermic response to several of these agents on Girk2 null mutant mice. Core body temperatures were measured through radiotelemetry, and animals were maintained in special temperature-regulated chambers to ensure the accuracy of the measurements. The resulting data indicate that the activation of GIRK2-containing potassium channels plays a significant role in hypothermia induced by the activation of serotonergic (5-HT(1A)), GABAergic (GABA(B)), muscarinic (m2), adenosine (A1), and mu, delta, and kappa opioid receptors. These channels also are involved in the alcohol-induced hypothermic response. These results have implications for the understanding of pharmacologically induced hypothermia and thermoregulatory mechanisms.

摘要

啮齿动物对多种单独的神经递质受体激动剂进行外周或脑室内注射后的低温反应已有充分记录。由于许多诱导低温的激动剂也已知会激活G蛋白门控钾通道(GIRK),我们研究了Girk2基因敲除突变小鼠对其中几种药物的低温反应。通过无线电遥测测量核心体温,并将动物饲养在特殊的温度调节室中以确保测量的准确性。所得数据表明,含GIRK2的钾通道的激活在由5-羟色胺能(5-HT(1A))、γ-氨基丁酸能(GABA(B))、毒蕈碱(m2)、腺苷(A1)以及μ、δ和κ阿片受体激活所诱导的低温中起重要作用。这些通道也参与酒精诱导的低温反应。这些结果对于理解药理学诱导的低温和体温调节机制具有重要意义。

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