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肿节风多糖对2型糖尿病小鼠的降血糖、降血脂及抗氧化作用

Hypoglycemic, hypolipidemic and antioxidant effects of Sarcandra glabra polysaccharide in type 2 diabetic mice.

作者信息

Liu Wei, Zheng Ying, Zhang Zhenzhen, Yao Wenbing, Gao Xiangdong

机构信息

State Key Laboratory of Natural Medicines, China Pharmaceutical University, Nanjing 210009, PR China.

出版信息

Food Funct. 2014 Nov;5(11):2850-60. doi: 10.1039/c4fo00430b.

Abstract

Sarcandra glabra (Thunb.) Nakai is a traditional Chinese herbal medicine and dietary supplement used for treating several diseases. The anti-diabetic activity of S. glabra polysaccharides is reported for the first time. The in vitro α-glucosidase inhibition assay indicated that the acidic S. glabra polysaccharide (SGP-2) has an IC50 of 87.06 ± 11.76 μg mL(-1), which was much lower than acarbose at 338.90 ± 46.86 μg mL(-1). Moreover, high fat diet (HFD) with streptozotocin (STZ) induced diabetic mice were administered SGP-2 (150, 300, or 600 mg kg(-1) per day, respectively) for 3 weeks. Postprandial blood glucose levels (PBGL), total cholesterol, triglyceride and free fatty acid levels in diabetic mice treated with SGP-2 were significantly decreased (p < 0.05) compared to those of the model group. The results of the oral glucose tolerance test (OGTT) and the homeostasis model assessment-insulin resistance (HOMA-IR) index indicated that SGP-2 could significantly improve (p < 0.05) the insulin resistance and glucose tolerance in diabetic mice. Furthermore, the activities of antioxidant enzymes, hexokinase and pyruvate kinase were significantly increased (p < 0.05) in SGP-2 treated groups. Thus we proposed that SGP-2 exerted hypoglycemic activity by relieving insulin resistance, reducing postprandial blood glucose levels and ameliorating lipid metabolism, as well as alleviating oxidative stress. These data suggested that SGP-2 with anti-hyperglycemic activity could be used in medicinal preparations for diabetes mellitus and its complications.

摘要

肿节风(学名:Sarcandra glabra (Thunb.) Nakai)是一种传统的中草药和膳食补充剂,用于治疗多种疾病。首次报道了肿节风多糖的抗糖尿病活性。体外α-葡萄糖苷酶抑制试验表明,酸性肿节风多糖(SGP-2)的IC50为87.06±11.76μg mL(-1),远低于阿卡波糖的338.90±46.86μg mL(-1)。此外,给高脂饮食(HFD)联合链脲佐菌素(STZ)诱导的糖尿病小鼠分别给予SGP-2(每天150、300或600mg kg(-1)),持续3周。与模型组相比,给予SGP-2治疗的糖尿病小鼠的餐后血糖水平(PBGL)、总胆固醇、甘油三酯和游离脂肪酸水平显著降低(p<0.05)。口服葡萄糖耐量试验(OGTT)和稳态模型评估-胰岛素抵抗(HOMA-IR)指数结果表明,SGP-2可显著改善(p<0.05)糖尿病小鼠的胰岛素抵抗和葡萄糖耐量。此外,SGP-2治疗组的抗氧化酶、己糖激酶和丙酮酸激酶活性显著增加(p<0.05)。因此,我们认为SGP-2通过缓解胰岛素抵抗、降低餐后血糖水平、改善脂质代谢以及减轻氧化应激来发挥降血糖活性。这些数据表明,具有降血糖活性的SGP-2可用于糖尿病及其并发症的药物制剂中。

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