Referenced in: none

Automatically associated channels: TASK1 , TREK1 , TWIK1

Title: Therapeutic targeting of two-pore-domain potassium (K2P) channels in the cardiovascular system.

Authors: Felix Wiedmann, Constanze Schmidt, Patrick Lugenbiel, Ingo Staudacher, Ann-Kathrin Rahm, Claudia Seyler, Patrick A Schweizer, Hugo A Katus, Dierk Thomas

Journal, date & volume: Clin. Sci., 2016 May 1 , 130, 643-50

PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/26993052

Abstract
The improvement of treatment strategies in cardiovascular medicine is an ongoing process that requires constant optimization. The ability of a therapeutic intervention to prevent cardiovascular pathology largely depends on its capacity to suppress the underlying mechanisms. Attenuation or reversal of disease-specific pathways has emerged as a promising paradigm, providing a mechanistic rationale for patient-tailored therapy. Two-pore-domain K(+) (K(2P)) channels conduct outward K(+) currents that stabilize the resting membrane potential and facilitate action potential repolarization. K(2P) expression in the cardiovascular system and polymodal K2P current regulation suggest functional significance and potential therapeutic roles of the channels. Recent work has focused primarily on K(2P)1.1 [tandem of pore domains in a weak inwardly rectifying K(+) channel (TWIK)-1], K(2P)2.1 [TWIK-related K(+) channel (TREK)-1], and K(2P)3.1 [TWIK-related acid-sensitive K(+) channel (TASK)-1] channels and their role in heart and vessels. K(2P) currents have been implicated in atrial and ventricular arrhythmogenesis and in setting the vascular tone. Furthermore, the association of genetic alterations in K(2P)3.1 channels with atrial fibrillation, cardiac conduction disorders and pulmonary arterial hypertension demonstrates the relevance of the channels in cardiovascular disease. The function, regulation and clinical significance of cardiovascular K(2P) channels are summarized in the present review, and therapeutic options are emphasized.