Empagliflozin inhibits coronary microvascular dysfunction and reduces cardiac pericyte loss in db/db mice
Endocrinology, Diabetes and Metabolism
empagliflozin
Empagliflozin
Cardiology
sodium-glucose cotransporter 2 inhibitors
Cardiovascular Medicine
Cardiac Metabolism
Biochemistry
pericytes
Endothelial stem cell
03 medical and health sciences
Diabetes mellitus
Endocrinology
0302 clinical medicine
In vitro
Recommendations for Cardiac Chamber Quantification by Echocardiography
Health Sciences
Diseases of the circulatory (Cardiovascular) system
Endothelial dysfunction
Clinical Studies on Coronary Stents and Revascularization
Internal medicine
Pericyte
diabetes
coronary microvascular dysfunction
Diabetic Cardiomyopathy
Management of Diabetes Mellitus and Cardiovascular Risk
Type 2 diabetes
3. Good health
Chemistry
RC666-701
Medicine
Surgery
Cardiology and Cardiovascular Medicine
DOI:
10.3389/fcvm.2022.995216
Publication Date:
2022-12-16T05:27:30Z
AUTHORS (13)
ABSTRACT
BackgroundCoronary microvascular dysfunction (CMD) is a pathophysiological feature of diabetic heart disease. However, whether sodium-glucose cotransporter 2 (SGLT2) inhibitors protect the cardiovascular system by alleviating CMD is not known.ObjectiveWe observed the protective effects of empagliflozin (EMPA) on diabetic CMD.Materials and methodsThe mice were randomly divided into a db/db group and a db/db + EMPA group, and db/m mice served as controls. At 8 weeks of age, the db/db + EMPA group was given empagliflozin 10 mg/(kg⋅d) by gavage for 8 weeks. Body weight, fasting blood glucose and blood pressure were dynamically observed. Cardiac systolic and diastolic function and coronary flow reserve (CFR) were detected using echocardiography. The coronary microvascular structure and distribution of cardiac pericytes were observed using immunofluorescence staining. Picrosirius red staining was performed to evaluate cardiac fibrosis.ResultsEmpagliflozin lowered the increased fasting blood glucose levels of the db/db group. The left ventricular ejection fraction, left ventricular fractional shortening, E/A ratio and E/e′ ratio were not significantly different between the three groups. CFR was decreased in the db/db group, but EMPA significantly improved CFR. In contrast to the sparse and abnormal expansion of coronary microvessels observed in the db/db group, the number of coronary microvessels was increased, and the capillary diameter was decreased in the db/db + EMPA group. The number and microvascular coverage of cardiac pericytes were reduced in the db/db mice but were improved by EMPA. The cardiac fibrosis was increased in db/db group and may alleviate by EMPA.ConclusionEmpagliflozin inhibited CMD and reduced cardiac pericyte loss in diabetic mice.
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