Shaker‐related voltage‐gated K+ channel expression and vasomotor function in human coronary resistance arteries. (9th January 2018)

• Record Type: Journal Article
• Authors: Nishijima, Yoshinori; Korishettar, Ankush; Chabowski, Dawid S.; Cao, Sheng; Zheng, Xiaodong; Gutterman, David D.; Zhang, David X.
• Is Part Of: Microcirculation. Volume 25:Number 1(2018)
• Page Start: n/a
• Page End: n/a
• Publication Date: 2018-01-09
• Subjects: coronary arteries -- coronary artery disease -- voltage‐gated potassium channels -- vasodilation; Biological transport -- Periodicals; Microcirculation -- Physiology -- Periodicals; 612.135
• DOI: 10.1111/micc.12431
• Languages: English
• ISSNs: 1073-9688

Abstract

Abstract: Objectives: KV channels are important regulators of vascular tone, but the identity of specific KV channels involved and their regulation in disease remain less well understood. We determined the expression of KV 1 channel subunits and their role in cAMP‐mediated dilation in coronary resistance arteries from subjects with and without CAD. Methods: HCAs from patients with and without CAD were assessed for mRNA and protein expression of KV 1 channel subunits with molecular techniques and for vasodilator response with isolated arterial myography. Results: Assays of mRNA transcripts, membrane protein expression, and vascular cell‐specific localization revealed abundant expression of KV 1.5 in vascular smooth muscle cells of non‐CAD HCAs. Isoproterenol and forskolin, two distinct cAMP‐mediated vasodilators, induced potent dilation of non‐CAD arterioles, which was inhibited by both the general KV blocker 4‐AP and the selective KV 1.5 blocker DPO‐1. The cAMP‐mediated dilation was reduced in CAD and was accompanied by a loss of or reduced contribution of 4‐AP‐sensitive KV channels. Conclusions: KV 1.5, as a major 4‐AP‐sensitive KV 1 channel expressed in coronary VSMCs, mediates cAMP‐mediated dilation in non‐CAD arterioles. The cAMP‐mediated dilation is reduced in CAD coronary arterioles, which is associated with impaired 4‐AP‐sensitive KV channel function.