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Endothelial ATP-Sensitive Potassium Channel Protects Against the Development of Hypertension and Atherosclerosis.

Authors :
Li, Yiwen
Aziz, Qadeer
Anderson, Naomi
Ojake, Leona
Tinker, Andrew
Source :
Hypertension (0194911X); Sep2020, Vol. 76 Issue 3, p776-784, 9p
Publication Year :
2020

Abstract

In the endothelium, ATP-sensitive potassium (KATP) channels are thought to couple cellular metabolism with membrane excitability, calcium entry, and endothelial mediator release. We hypothesized that endothelial KATP channels have a broad role protecting against high blood pressure and atherosclerosis. Endothelial-specific Kir6.1 KO mice (eKO) and eKO mice on an apolipoprotein E KO background were generated (A-eKO) to investigate the role of KATP channels in the endothelium. Basal blood pressure was not elevated in eKO mice. However, when challenged with a high-salt diet and the eNOS inhibitor L-NAME, eKO mice became more hypertensive than their littermate controls. In aorta, NO release at least partly contributes to the endothelium-dependent vasorelaxation induced by pinacidil. In A-eKO mice atherosclerotic plaque density was significantly greater than in their littermate controls when challenged with a high-fat diet, particularly in the aortic arch region. Levels of endothelial dysfunction markers were higher in eKO compared with WT mice; however, these were not significant for A-eKO mice compared with their littermate controls. Furthermore, decreased vascular reactivity was observed in the mesenteric arteries of A-eKO mice, but not in aorta when on a high-fat diet. Our data support a role for endothelial Kir6.1-containing KATP channels in the endothelial protection against environmental stressors: the maintenance of blood pressure homeostasis in response to high salt and endothelial integrity when challenged with a high-fat diet. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
0194911X
Volume :
76
Issue :
3
Database :
Supplemental Index
Journal :
Hypertension (0194911X)
Publication Type :
Academic Journal
Accession number :
145105619
Full Text :
https://doi.org/10.1161/HYPERTENSIONAHA.120.15355