Lamas J Antonio, Fernández-Fernández Diego
Laboratory of Neuroscience, Biomedical Research Center (CINBIO), University of Vigo, Vigo, Galicia, Spain.
Neural Regen Res. 2019 Aug;14(8):1293-1308. doi: 10.4103/1673-5374.253506.
TWIK-related potassium channels (TREK) belong to a subfamily of the two-pore domain potassium channels family with three members, TREK1, TREK2 and TWIK-related arachidonic acid-activated potassium channels. The two-pore domain potassium channels is the last big family of channels being discovered, therefore it is not surprising that most of the information we know about TREK channels predominantly comes from the study of heterologously expressed channels. Notwithstanding, in this review we pay special attention to the limited amount of information available on native TREK-like channels and real neurons in relation to neuroprotection. Mainly we focus on the role of free fatty acids, lysophospholipids and other neuroprotective agents like riluzole in the modulation of TREK channels, emphasizing on how important this modulation may be for the development of new therapies against neuropathic pain, depression, schizophrenia, epilepsy, ischemia and cardiac complications.
TWIK相关钾通道(TREK)属于双孔结构域钾通道家族的一个亚家族,有三个成员,即TREK1、TREK2和TWIK相关花生四烯酸激活钾通道。双孔结构域钾通道是最后一个被发现的大通道家族,因此我们所了解的关于TREK通道的大部分信息主要来自对异源表达通道的研究也就不足为奇了。尽管如此,在本综述中,我们特别关注与神经保护相关的天然TREK样通道和真实神经元的有限信息。我们主要关注游离脂肪酸、溶血磷脂和其他神经保护剂(如利鲁唑)在TREK通道调节中的作用,强调这种调节对于开发针对神经性疼痛、抑郁症、精神分裂症、癫痫、缺血和心脏并发症的新疗法可能有多重要。