Contribution of KV1.5 Channel to Hydrogen Peroxide–Induced Human Arteriolar Dilation and Its Modulation by Coronary Artery Disease. Issue 4 (17th February 2017)

• Record Type: Journal Article
• Authors: Nishijima, Yoshinori; Cao, Sheng; Chabowski, Dawid S.; Korishettar, Ankush; Ge, Alyce; Zheng, Xiaodong; Sparapani, Rodney; Gutterman, David D.; Zhang, David X.
• Is Part Of: Circulation research. Volume 120:Issue 4(2017)
• Publication Date: 2017-02-17
• Subjects: arterioles -- endothelium -- hydrogen peroxide -- potassium channels -- vasodilation; Cardiovascular system -- Periodicals; Blood -- Circulation -- Periodicals; Blood Circulation; Cardiovascular System; Vascular Diseases; Sang -- Circulation -- Périodiques; Appareil cardiovasculaire -- Périodiques; 612.1
• DOI: 10.1161/CIRCRESAHA.116.309491
• Languages: English
• ISSNs: 0009-7330

Abstract

Abstract : Rationale: : Hydrogen peroxide (H2 O2 ) regulates vascular tone in the human microcirculation under physiological and pathophysiological conditions. It dilates arterioles by activating large-conductance Ca 2+ -activated K + channels in subjects with coronary artery disease (CAD), but its mechanisms of action in subjects without CAD (non-CAD) when compared with those with CAD remain unknown. Objective: : We hypothesize that H2 O2 -elicited dilation involves different K + channels in non-CAD versus CAD, resulting in an altered capacity for vasodilation during disease. Methods and Results: : H2 O2 induced endothelium-independent vasodilation in non-CAD adipose arterioles, which was reduced by paxilline, a large-conductance Ca 2+ -activated K + channel blocker, and by 4-aminopyridine, a voltage-gated K + (KV ) channel blocker. Assays of mRNA transcripts, protein expression, and subcellular localization revealed that KV 1.5 is the major KV 1 channel expressed in vascular smooth muscle cells and is abundantly localized on the plasma membrane. The selective KV 1.5 blocker diphenylphosphine oxide-1 and the KV 1.3/1.5 blocker 5-(4-phenylbutoxy)psoralen reduced H2 O2 -elicited dilation to a similar extent as 4-aminopyridine, but the selective KV 1.3 blocker phenoxyalkoxypsoralen-1 was without effect. In arterioles from CAD subjects, H2 O2 -induced dilation was significantly reduced, and this dilation was inhibited by paxilline but not by 4-aminopyridine, diphenylphosphine oxide-1, or 5-(4-phenylbutoxy)psoralen. KV 1.5 cell membrane localization and diphenylphosphine oxide-1–sensitive K + currents were markedly reduced in isolated vascular smooth muscle cells from CAD arterioles, although mRNA or total cellular protein expression was largely unchanged. Conclusions: : In human arterioles, H2 O2 -induced dilation is impaired in CAD, which is associated with a transition from a combined large-conductance Ca 2+ -activated K + - and KV (KV 1.5)-mediated vasodilation toward a large-conductance Ca 2+ –activated K + –predominant mechanism of dilation. Loss of KV 1.5 vasomotor function may play an important role in microvascular dysfunction in CAD or other vascular diseases. Abstract : Supplemental Digital Content is available in the text.