首页> 美国卫生研究院文献>The Journal of Neuroscience >G-Protein-Gated Potassium (GIRK) Channels Containing the GIRK2 Subunit Are Control Hubs for Pharmacologically Induced Hypothermic Responses
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G-Protein-Gated Potassium (GIRK) Channels Containing the GIRK2 Subunit Are Control Hubs for Pharmacologically Induced Hypothermic Responses

机译:包含GIRK2亚基的G蛋白门控钾(GIRK)通道是药理学上引起的低温反应的控制中心。

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摘要

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-HT1A), GABAergic (GABAB), muscarinic (m2), adenosine (A1), and μ, δ, and κ 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.
机译:啮齿动物对许多单独的神经递质受体激动剂的外周或脑室内注射的低温反应已得到充分证明。由于还已知许多诱导体温过低的激动剂会激活G蛋白门控钾(GIRK)通道,因此我们在Girk2空突变小鼠上研究了对其中几种药物的低温反应。核心体温是通过无线电遥测法测量的,动物被关在特殊的温度调节室中以确保测量的准确性。结果数据表明,含GIRK2的钾离子通道的激活在血清素能(5-HT1A),GABA能(GABAB),毒蕈碱(m2),腺苷(A1)和μ,δ激活引起的体温过低中起重要作用和κ阿片受体。这些通道也参与酒精诱导的低温反应。这些结果对理解药理学引起的体温过低和温度调节机制具有启示意义。

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