| Literature DB >> 26588045 |
Delphine Vivier1,2, Khalil Bennis1,2, Florian Lesage3, Sylvie Ducki1,2.
Abstract
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.Entities:
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Year: 2015 PMID: 26588045 DOI: 10.1021/acs.jmedchem.5b00671
Source DB: PubMed Journal: J Med Chem ISSN: 0022-2623 Impact factor: 7.446