Borapetoside E, a Clerodane Diterpenoid Extracted from Tinospora crispa, Improves Hyperglycemia and Hyperlipidemia in High-Fat-Diet-Induced Type 2 Diabetes Mice.
Yuhui XuYanfen NiuYuan GaoFang WangWanying QinYanting LuJing HuLi PengJikai LiuWen-Yong XiongPublished in: Journal of natural products (2017)
An insidious increase in the incidence of obesity, insulin resistance, and hyperlipidemia has led to an epidemic of type 2 diabetes worldwide. Tinospora crispa (T. crispa) is a familiar plant traditionally used in herbal medicine for diabetes; however, the major active ingredients of this plant are still unclear. In this study, we identified the therapeutic effects of borapetoside E, a small molecule extracted from T. crispa, in high-fat-diet (HFD)-induced obesity in mice. The therapeutic effects of borapetoside E in HFD-induced obese mice were assessed physiologically, histologically, and biochemically following intraperitoneal injection. Furthermore, we analyzed the expression of glucose and lipid metabolism-related genes and proteins in borapetoside E-treated obese mice. Compared with vehicle-treated mice, borapetoside E markedly improved hyperglycemia, insulin resistance, hepatic steatosis, hyperlipidemia, and oxygen consumption in obese mice, and the effects were comparable to or better than the drug metformin. In addition, borapetoside E suppressed the expression of sterol regulatory element binding proteins (SREBPs) and their downstream target genes related to lipid synthesis in the liver and adipose tissue. Borapetoside E showed beneficial effects in vivo, demonstrating that borapetoside E may be a potential therapy for the treatment of diet-induced type 2 diabetes and related metabolic syndromes.
Keyphrases
- insulin resistance
- high fat diet induced
- high fat diet
- type diabetes
- adipose tissue
- glycemic control
- metabolic syndrome
- skeletal muscle
- polycystic ovary syndrome
- diabetic rats
- small molecule
- poor prognosis
- cardiovascular disease
- high glucose
- drug induced
- binding protein
- blood glucose
- emergency department
- risk factors
- fatty acid
- endothelial cells
- climate change
- combination therapy
- gene expression
- risk assessment
- physical activity
- protein protein
- adverse drug