College of Chemistry and Chemical Engineering, Lanzhou University, 222 Tianshui Road, Lanzhou 730000, China.
Can J Physiol Pharmacol. 2010 Jan;88(1):64-72. doi: 10.1139/Y09-098.
Hedysarum polybotrys polysaccharide (HPS) is the principal active fraction responsible for the antidiabetic properties of this species. The aim of this study was to determine the antidiabetic properties of 4 purified fractions of different molecular weight range HPSs (HPS1, HPS2, HPS3, HPS4). HPS3 was selected for examination of its hypoglycemic mechanism because of its significant hypoglycemic effect in alloxan-induced diabetic mice. The changes in blood glucose levels and oral glucose tolerance tests (OGTT) showed that hypoglycemia was more pronounced in HPS3-treated groups than in the diabetes mellitus model (DM) control group. The interleukin-6, tumor necrosis factor-alpha, leptin, and free fatty acid levels were significantly lower in the HPS3-treated groups and HPS3 + metformin (HPS3+MET) group than in the DM control group, while plasma insulin, hepatic glycogen, superoxide dismutase, and nitric oxide synthetase activity were significantly higher. Treatment with HPS3 or HPS3+MET also significantly lowered malonaldehyde levels compared with the DM control group, while it elevated the nitric oxide and total antioxidant capacity. HPS3 altered the plasma lipid levels by lowering cholesterol and triglyceride concentrations, while elevating the plasma high-density lipoprotein cholesterol level. Therefore, these results suggest that HPS3 may partly ameliorate hyperglycemia and hyperlipidemia associated with type 2 diabetes through increased insulin secretion, inhibition of lipid peroxidation, promotion of sensitivity to insulin, suppression of gluconeogenesis and reduction in the biosynthesis fatty acid, cholesterol and cell cytokines related to insulin resistance, and it could be a useful adjunct therapy to a proven first-line therapy for type 2 diabetes using metformin.
红芪多糖(HPS)是该物种具有降血糖作用的主要活性成分。本研究旨在确定 4 种不同分子量范围 HPS (HPS1、HPS2、HPS3、HPS4)的纯化部分的降血糖特性。由于 HPS3 在四氧嘧啶诱导的糖尿病小鼠中具有显著的降血糖作用,因此选择其来研究其降血糖机制。血糖水平变化和口服葡萄糖耐量试验(OGTT)表明,HPS3 治疗组的低血糖作用比糖尿病模型(DM)对照组更为明显。HPS3 治疗组和 HPS3+二甲双胍(HPS3+MET)组的白细胞介素-6、肿瘤坏死因子-α、瘦素和游离脂肪酸水平明显低于 DM 对照组,而血浆胰岛素、肝糖原、超氧化物歧化酶和一氧化氮合酶活性明显升高。与 DM 对照组相比,HPS3 或 HPS3+MET 治疗还显著降低了丙二醛水平,同时升高了一氧化氮和总抗氧化能力。HPS3 通过降低胆固醇和甘油三酯浓度来改变血浆脂质水平,同时升高血浆高密度脂蛋白胆固醇水平。因此,这些结果表明,HPS3 可能通过增加胰岛素分泌、抑制脂质过氧化、促进胰岛素敏感性、抑制糖异生和减少与胰岛素抵抗相关的脂肪酸、胆固醇和细胞细胞因子的生物合成,部分改善 2 型糖尿病伴发的高血糖和高血脂,它可能是二甲双胍等已被证实的 2 型糖尿病一线治疗的有用辅助治疗方法。