Endothelial Kir2 channel dysfunction in aged cerebral parenchymal arterioles

Author:

Polk Felipe D.1ORCID,Hakim Md A.2ORCID,Silva Josiane F.1ORCID,Behringer Erik J.2ORCID,Pires Paulo W.13ORCID

Affiliation:

1. Department of Physiology, University of Arizona College of Medicine Tucson, Tucson, Arizona, United States

2. Department of Basic Sciences, Loma Linda University, Loma Linda, California, United States

3. Sarver Heart Center and BIO5 Institute, University of Arizona College of Medicine Tucson, Tucson, Arizona, United States

Abstract

Advanced age in mice (>2 yr, similar to a 70- to 80-yr-old human) impairs P2Y and Kir2 channel-induced dilation. Reductions in endothelial Kir2 activity were associated with lower vasodilatory response to purinergic receptor activation and increased resting myogenic tone of cerebral arterioles. Paradoxically, vasodilation following Kir2 activation was larger in aged cerebral arterioles, and unaffected by endothelium removal, suggesting a possible compensation by smooth muscle Kir2 channels. However, this compensation was not sufficient to restore purinergic dilation.

Funder

Alzheimer's Association

HHS | NIH | National Heart, Lung, and Blood Institute

HHS | NIH | National Institute on Aging

Publisher

American Physiological Society

Subject

Physiology (medical),Cardiology and Cardiovascular Medicine,Physiology

Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Functional, Structural and Proteomic Effects of Ageing in Resistance Arteries;International Journal of Molecular Sciences;2024-02-23

2. To err, KIR2 that is, on the side of vasodilation in aging;American Journal of Physiology-Heart and Circulatory Physiology;2023-12-01

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