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Borapetoside E, a Clerodane Diterpenoid Extracted from Tinospora crispa, Improves Hyperglycemia and Hyperlipidemia in High-Fat-Diet-Induced Type 2 Diabetes Mice
Journal of Natural Products ( IF 3.3 ) Pub Date : 2017-07-25 00:00:00 , DOI: 10.1021/acs.jnatprod.7b00365
Yuhui Xu 1, 2 , Yanfen Niu 1, 2, 3 , Yuan Gao 4, 5 , Fang Wang 1, 2 , Wanying Qin 1, 2 , Yanting Lu 1, 2 , Jing Hu 1, 2 , Li Peng 1, 2 , Jikai Liu 6 , Wenyong Xiong 1, 2
Affiliation  

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.

中文翻译:

Borapetoside E,一种从香茅(Tinospora crispa)提取的氯丹定双萜,可改善高脂饮食诱导的2型糖尿病小鼠的高血糖和高脂血症。

肥胖症,胰岛素抵抗和高脂血症的发生率急剧增加已导致全世界2型糖尿病的流行。Tinospora crispaT. crispa)是一种熟悉的植物,传统上用于治疗糖尿病的草药;但是,该植物的主要活性成分仍不清楚。在这项研究中,我们发现borapetoside E的治疗效果,小分子摘自T.皱,是由高脂饮食(HFD)引起的小鼠肥胖引起的。腹膜内注射后,在生理,组织和生化方面评估了raprapetoside E在HFD诱导的肥胖小鼠中的治疗作用。此外,我们分析了在borapetoside E治疗的肥胖小鼠中葡萄糖和脂质代谢相关基因和蛋白质的表达。与赋形剂治疗的小鼠相比,波普拉托甙E显着改善了肥胖小鼠的高血糖症,胰岛素抵抗,肝脂肪变性,高脂血症和耗氧量,其效果与二甲双胍相当或更好。此外,波拉托甙E抑制了固醇调节元件结合蛋白(SREBPs)的表达及其与肝脏和脂肪组织中脂质合成有关的下游靶基因。菜籽糖苷E显示出有益的作用在体内,证明了波拉贝托E可能是治疗饮食引起的2型糖尿病和相关代谢综合征的潜在疗法。
更新日期:2017-07-25
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