Affiliation:
1. Department of Pharmacology and Toxicology, University of Mississippi Medical Center, Jackson, Mississippi
2. Department of Anesthesiology, Medical College of Wisconsin, Milwaukee, Wisconsin
Abstract
This study demonstrates that luseogliflozin, a sodium-glucose cotransporter-2 inhibitor, improved CBF autoregulation in association with reduced vascular oxidative stress and AGEs production in the cerebrovasculature of 18-mo-old DM rats. SGLT2i also prevented BBB leakage, impaired functional hyperemia, neurodegeneration, and cognitive impairment seen in DM rats. Luseogliflozin did not have direct constrictive effects on VSMCs and MCAs isolated from normal rats. These results provide evidence that normalization of hyperglycemia with an SGLT2i can reverse cerebrovascular dysfunction and cognitive impairments in rats with long-standing hyperglycemia, possibly by ameliorating oxidative stress-caused vascular damage.
Funder
University of Mississippi Medical Center
American Heart Association
HHS | NIH | National Institute on Aging
HHS | NIH | National Institute of General Medical Sciences
HHS | NIH | National Heart, Lung, and Blood Institute
Publisher
American Physiological Society
Subject
Physiology (medical),Cardiology and Cardiovascular Medicine,Physiology
Cited by
15 articles.
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