Zhang Chenyang, Han Meixin, Zhang Xuelian, Tong Hongna, Sun Xiaobo, Sun Guibo
Institute of Medicinal Plant Development, Peking Union Medical College and Chinese Academy of Medical Sciences, Beijing, People's Republic of China.
College of Pharmacy, Harbin University of Commerce, Harbin, People's Republic of China.
J Inflamm Res. 2022 Jan 5;15:71-83. doi: 10.2147/JIR.S348866. eCollection 2022.
Obesity and diabetes are often accompanied by chronic inflammation and insulin resistance, which lead to complications such as diabetic cardiomyopathy. Ginsenoside Rb1 has been used to treat diabetes and obesity and reduce inflammation as well as risk of heart diseases. However, the role of ginsenoside Rb1 in treating diabetic cardiomyopathy remains unclear.
Diabetic mice were administered ginsenoside Rb1 for 12 weeks, and their body weight, body fat, and blood glucose levels as well as and serum insulin, lipids, and adipocytokine levels were assessed. Lipid accumulation, pathological morphology of the adipose tissue, liver, and heart were examined. Western blot and qRT-PCR were performed to investigate the molecular changes in response to ginsenoside Rb1 treatment.
Ginsenoside Rb1 treatment significantly reduced body weight and body fat, attenuated hyperglycemia and hyperlipidemia, and ameliorated insulin resistance and abnormal levels of adipocytokines in diabetic mice. In addition, lipid accumulation and inflammation reduced while the functions of heart improved in the ginsenoside Rb1-treated group. Furthermore, antioxidant function improved in the ginsenoside Rb1-treated diabetic hearts. PCR and Western blotting analyses revealed that the lipid-lowering effect of ginsenoside Rb1 and the resulting improvement of cardiac function could be attributed to the adipocytokine pathway, which promoted energy homeostasis and alleviated cardiac dysfunction.
Ginsenoside Rb1 lowered lipid levels in a adipocytokine-mediated manner and attenuated hyperglycemia/hyperlipidemia-induced oxidative stress, hypertrophy, inflammation, fibrosis, and apoptosis in cardiomyocytes.
肥胖和糖尿病常伴有慢性炎症和胰岛素抵抗,进而导致糖尿病性心肌病等并发症。人参皂苷Rb1已被用于治疗糖尿病和肥胖症,并减轻炎症以及心脏病风险。然而,人参皂苷Rb1在治疗糖尿病性心肌病中的作用仍不清楚。
给糖尿病小鼠施用人参皂苷Rb1 12周,评估其体重、体脂、血糖水平以及血清胰岛素、脂质和脂肪细胞因子水平。检查脂质积累、脂肪组织、肝脏和心脏的病理形态。进行蛋白质印迹和qRT-PCR以研究人参皂苷Rb1治疗后的分子变化。
人参皂苷Rb1治疗显著降低了糖尿病小鼠的体重和体脂,减轻了高血糖和高血脂,改善了胰岛素抵抗和脂肪细胞因子异常水平。此外,人参皂苷Rb1治疗组的脂质积累和炎症减少,心脏功能改善。此外,人参皂苷Rb1治疗的糖尿病心脏的抗氧化功能得到改善。PCR和蛋白质印迹分析表明,人参皂苷Rb1的降脂作用以及由此导致的心脏功能改善可归因于脂肪细胞因子途径,该途径促进能量稳态并减轻心脏功能障碍。
人参皂苷Rb1以脂肪细胞因子介导的方式降低脂质水平,并减轻高血糖/高血脂诱导的心肌细胞氧化应激、肥大、炎症、纤维化和凋亡。