Quercetin Reverses Cardiac Systolic Dysfunction in Mice Fed with a High-Fat Diet: Role of Angiogenesis

• Published in: Oxidative medicine and cellular longevity Vol. 2021; no. 1; p. 8875729
• Main Authors: Yu, Shasha, Kim, Seo Rin, Jiang, Kai, Ogrodnik, Mikolaj, Zhu, Xiang Y., Ferguson, Christopher M., Tchkonia, Tamara, Lerman, Amir, Kirkland, James L., Lerman, Lilach O.
• Format: Journal Article
• Language: English
• Published: United States Hindawi 2021; Hindawi Limited
• Subjects: Animals; Biomarkers - metabolism; Body temperature; Cardiac function; Cardiomegaly - pathology; Cardiomegaly - physiopathology; Cellular Senescence - drug effects; Diet; Diet, High-Fat; Feeding Behavior; Fibrosis; Gene expression; Heart; Heart - physiopathology; Histology; Human Umbilical Vein Endothelial Cells - drug effects; Human Umbilical Vein Endothelial Cells - metabolism; Humans; Insulin resistance; Kinases; Laboratories; Lipid Metabolism - drug effects; Magnetic resonance imaging; Male; Mice; Mice, Inbred C57BL; Myocardium - pathology; Myocytes, Cardiac - drug effects; Myocytes, Cardiac - metabolism; Myocytes, Cardiac - pathology; Neovascularization, Physiologic - drug effects; Obesity; Oxidative stress; Oxidative Stress - drug effects; Quercetin - pharmacology; Senescence; Systole - drug effects; Vascular endothelial growth factor; Vascular Remodeling - drug effects; Germany
• ISSN: 1942-0900; 1942-0994
• DOI: 10.1155/2021/8875729

Global consumption of high-fat diets (HFD) is associated with an increased incidence of cardiometabolic syndrome and cardiac injury, warranting identification of cardioprotective strategies. Cardioprotective effects of quercetin (Q) have mostly been evaluated in ischemic heart disease models and attributed to senolysis. We hypothesized that Q could alleviate murine cardiac damage caused by HFD by restoring the myocardial microcirculation. C57BL/6J mice were fed standard chow or HFD for 6 months and then treated with Q (50 mg/kg) or vehicle 5-day biweekly for 10 additional weeks. Left ventricular (LV) cardiac function was studied in vivo using magnetic resonance imaging, and intramyocardial fat deposition, microvascular density, oxidative stress, and senescence were analyzed ex vivo. Additionally, direct angiogenic effects of Q were studied in vitro in HUVECs. HFD increased body weight, heart weight, total cholesterol, and triglyceride levels, whereas Q normalized heart weight and triglycerides. LV ejection fraction was lower in HFD vs. control mice (56.20±15.8% vs. 73.38±5.04%, respectively, P<0.05), but improved in HFD + Q mice (67.42±7.50%, P<0.05, vs. HFD). Q also prevented cardiac fat accumulation and reduced HFD-induced cardiac fibrosis, cardiomyocyte hypertrophy, oxidative stress, and vascular rarefaction. Cardiac senescence was not observed in any group. In vitro, ox-LDL reduced HUVEC tube formation activity, which Q effectively improved. Quercetin may directly induce angiogenesis and decrease myocardial oxidative stress, which might account for its cardioprotective effects in the murine HFD-fed murine heart independently from senolytic activity. Furthermore, its beneficial effects might be partly attributed to a decrease in plasma triglycerides and intramyocardial fat deposition.