Shaker-related voltage-gated K+ channel expression and vasomotor function in human coronary resistance arteries

Microcirculation. 2018 Jan;25(1):10.1111/micc.12431. doi: 10.1111/micc.12431.

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.

Keywords: coronary arteries; coronary artery disease; vasodilation; voltage-gated potassium channels.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Arterioles / physiology
  • Cardiovascular Diseases / etiology
  • Case-Control Studies
  • Coronary Vessels / chemistry*
  • Cyclic AMP / physiology
  • Humans
  • Potassium Channels, Voltage-Gated / metabolism*
  • Protein Subunits
  • RNA, Messenger / analysis
  • Vasodilation / drug effects*

Substances

  • Potassium Channels, Voltage-Gated
  • Protein Subunits
  • RNA, Messenger
  • Cyclic AMP