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孤啡肽/孤啡肽FQ受体与G蛋白激活的钾离子(GIRK)通道的功能偶联。

Functional coupling of the nociceptin/orphanin FQ receptor with the G-protein-activated K+ (GIRK) channel.

作者信息

Ikeda K, Kobayashi K, Kobayashi T, Ichikawa T, Kumanishi T, Kishida H, Yano R, Manabe T

机构信息

Laboratory for Cellular Information Processing, Institute of Physical and Chemical Research (RIKEN), Saitama, Japan.

出版信息

Brain Res Mol Brain Res. 1997 Apr;45(1):117-26. doi: 10.1016/s0169-328x(96)00252-5.

Abstract

Nociceptin/orphanin FQ is a heptadecapeptide which was recently isolated from brains. It induces hyperalgesia, in contrast to the analgesic effects of opioid ligands, although it and its receptor structurally resemble opioid peptides and opioid receptors, respectively. To investigate the molecular mechanism underlying nociceptin/orphanin FQ actions, we performed Xenopus oocyte expression assays, in situ hybridization histochemistry and electrophysiological analyses of neurons. We found that the nociceptin/orphanin FQ receptor is functionally coupled with the G-protein-activated K+ (GIRK) channel in Xenopus oocytes, and that the receptor mRNA and GIRK1 mRNA co-exist in various neurons, including hippocampal pyramidal cells. Furthermore, we found that nociceptin/orphanin FQ induces hyperpolarizing currents via inward-rectifier K+ channels in hippocampal pyramidal cells, suggesting that the nociceptin/orphanin FQ receptor couples with the GIRK channel in this region. We conclude that the nociceptin/orphanin FQ receptor couples with the GIRK channel in various neurons, including hippocampal pyramidal cells, thereby modulating neuronal excitability.

摘要

孤啡肽是一种十七肽,最近从大脑中分离出来。与阿片样物质配体的镇痛作用相反,它会诱发痛觉过敏,尽管它及其受体在结构上分别类似于阿片肽和阿片受体。为了研究孤啡肽作用的分子机制,我们进行了非洲爪蟾卵母细胞表达试验、原位杂交组织化学以及神经元的电生理分析。我们发现,在非洲爪蟾卵母细胞中,孤啡肽受体与G蛋白激活的钾离子(GIRK)通道功能偶联,并且该受体mRNA和GIRK1 mRNA共存于包括海马锥体细胞在内的各种神经元中。此外,我们发现孤啡肽通过海马锥体细胞中的内向整流钾离子通道诱导超极化电流,这表明孤啡肽受体在该区域与GIRK通道偶联。我们得出结论,孤啡肽受体在包括海马锥体细胞在内的各种神经元中与GIRK通道偶联,从而调节神经元兴奋性。

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