Vasorelaxation by hydrogen sulphide involves activation of Kv7 potassium channels

Hydrogen sulphide (H2S) has been recently hypothesized to be an endogenous adipocyte-derived relaxing factor, evoking vasorelaxation of conductance and resistance vessels. Although the activation of ATP-sensitive potassium channels is known to play a central role in H2S-induced vasorelaxation, activation of vascular K(v)7 voltage-gated potassium channels has also been suggested. To investigate this possibility, the ability of selective activators and blockers of distinct classes of potassium channels to affect vasodilation induced by the H2S-donor NaHS, as well as NaHS-induced Rb+ efflux in endothelium-denuded rat aortic rings, was investigated. NaHS-induced changes of membrane potential were fluorimetrically assessed on human vascular smooth muscle (VSM) cells. Modulation of K(v)7.4 channels by NaHS was assessed by electrophysiological studies, upon their heterologous expression in CHO cells. In isolated aortic rings, NaHS evoked vasorelaxing responses associated with an increase of Rb+-efflux. NaHS promoted membrane hyperpolarization of human VSM cells. These effects were antagonized by selective blockers of K(v)7 channels. The H2S-donor caused a left-shift of current activation threshold of K(v)7.4 channels expressed in CHO cells. Altogether, these results suggest that the activation of K(v)7.4 channels is a key mechanism in the vascular effects of H2S. Given the relevant roles played by K(v)7.4 channels in VSM contractility and by H2S in circulatory homeostasis regulation, these findings provide interesting insights to improve our understanding of H2S pathophysiology and to focus on K(v)7.4 channels as novel targets for therapeutic approaches via the H2S-system. (C) 2013 Elsevier Ltd. All rights reserved.