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Anti-diabetic effect of ginsenoside Rb 3 in alloxan-induced diabetic mice

机译:人参皂苷Rb 3在四氧嘧啶诱导的糖尿病小鼠中的抗糖尿病作用

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摘要

As one of the main active component of protopanaxdiol type ginsenosides, ginsenoside Rb 3 is rarely reported in the treatment of diabetes. The anti-diabetic activity of ginsenoside Rb 3 was investigated in a model of alloxan-induced diabetic mice in the present study. The physiological parameter such as fasting blood glucose level, oral glucose tolerance, body weight, food intake and water intake were measured. Glucose consumption in C2C12 myotubes was also determined in order to investigate the molecular mechanism of ginsenoside Rb 3 in anti-diabetes. The alloxan-induced diabetic mice were treated with ginsenoside Rb 3 for 2 weeks at doses of 5 mg/kg, 15 mg/kg and 25 mg/kg. After 2 weeks treatment of ginsenoside Rb 3, the fasting blood glucose levels of DG 15 and DG 25 were respectively reduced by 36.70% and 37.50% compared to control group. At a dose of 25 mg/kg, oral glucose tolerance was significantly improved compared to control group (P 0.05). The AUC decreased by 34.47% (from 2442 ± 291 mmol·min/L to 1600 ± 109 mmol·min/L). Both food intake and water intake were remarkably lowered. The injury of pancreas tissues was repaired, which was observed by using HE staining and optic microscope. In vitro, at concentrations of 100 and 200 μM, ginsenoside Rb 3 increased glucose consumption in C2C12 myotubes by 76.83% and 97.20%, respectively, as compared to the control group. However, the body weight of diabetic mice was not significantly altered. In conclusion, our results showed that ginsenoside Rb 3 reduced fasting blood glucose level, food intake, water intake, improved oral glucose tolerance, and repaired injured pancreas tissues of alloxan-induced diabetic mice. Therefore, it was suggested that ginsenoside possesses the potential of the clinical use in preventing and treating diabetes.
机译:人参皂苷Rb 3作为人参皂苷原蛋白的主要活性成分之一,在糖尿病的治疗中很少报道。在本研究中,在四氧嘧啶诱导的糖尿病小鼠模型中研究了人参皂甙Rb 3的抗糖尿病活性。测量诸如空腹血糖水平,口服葡萄糖耐量,体重,食物摄入和水摄入​​等生理参数。为了研究人参皂苷Rb 3在抗糖尿病中的分子机制,还确定了C2C12肌管中的葡萄糖消耗。用人参皂苷Rb 3以5 mg / kg,15 mg / kg和25 mg / kg的剂量对四氧嘧啶诱导的糖尿病小鼠进行治疗2周。人参皂苷Rb 3治疗2周后,与对照组相比,DG 15和DG 25的空腹血​​糖水平分别降低了36.70%和37.50%。与对照组相比,在25 mg / kg的剂量下,口服葡萄糖耐量显着提高(P <0.05)。 AUC降低了34.47%(从2442±291 mmol·min / L降至1600±109 mmol·min / L)。食物摄入和水摄入​​均显着降低。修复胰腺组织损伤,用HE染色和光学显微镜观察。在体外,与对照组相比,人参皂甙Rb 3在100和200μM的浓度下分别使C2C12肌管中的葡萄糖消耗增加了76.83%和97.20%。但是,糖尿病小鼠的体重没有明显改变。总之,我们的结果表明,人参皂甙Rb 3降低了四氧嘧啶诱导的糖尿病小鼠的空腹血糖水平,食物摄入,水摄入,改善了口服葡萄糖耐量并修复了受损的胰腺组织。因此,建议人参皂苷具有预防和治疗糖尿病的临床用途的潜力。

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