化学
钾通道
门控
离子通道
生物物理学
配体门控离子通道
膜电位
神经科学
生物化学
受体
生物
作者
Delphine Vivier,Khalil Bennis,Florian Lesage,Sylvie Ducki
标识
DOI:10.1021/acs.jmedchem.5b00671
摘要
Potassium (K(+)) channels are membrane proteins expressed in most living cells that selectively control the flow of K(+) ions. More than 80 genes encode the K(+) channel subunits in the human genome. The TWIK-related K(+) channel (TREK-1) belongs to the two-pore domain K(+) channels (K2P) and displays various properties including sensitivity to physical (membrane stretch, acidosis, temperature) and chemical stimuli (signaling lipids, volatile anesthetics). The distribution of TREK-1 in the central nervous system, coupled with the physiological consequences of its opening and closing, leads to the emergence of this channel as an attractive therapeutic target. We review the TREK-1 channel, its structural and functional properties, and the pharmacological agents (agonists and antagonists) able to modulate its gating.
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