伤害感受器
神经科学
离子通道
钾通道
偏头痛
痛觉
有害刺激
亚科
化学
心理学
受体
伤害
生物物理学
医学
生物
内科学
麻醉
基因
生物化学
作者
Pablo Ávalos Prado,Anne-Amandine Chassot,Arnaud Landra-Willm,Guillaume Sandoz
标识
DOI:10.1016/j.neulet.2022.136494
摘要
The ability to sense pain signals is closely linked to the activity of ion channels expressed in nociceptors, the first neurons that transduce noxious stimuli into pain. Among these ion channels, TREK1, TREK2 and TRAAK from the TREK subfamily of the Two-Pore-Domain potassium (K2P) channels, are hyperpolarizing channels that render neurons hypoexcitable. They are regulated by diverse physical and chemical stimuli as well as neurotransmitters through G-protein coupled receptor activation. Here, we review the molecular mechanisms underlying these regulations and their functional relevance in pain and migraine induction.
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