Antidiabetic properties of purified polysaccharide from Hedysarum polybotrys

被引:28
作者
Hu, Fangdi [1 ,2 ]
Li, Xiaodong [3 ]
Zhao, Lianggong [4 ]
Feng, Shilan [1 ,5 ]
Wang, Chunming [2 ]
机构
[1] Lanzhou Univ, Sch Pharmacol, Lanzhou 730000, Peoples R China
[2] Lanzhou Univ, Coll Chem & Chem Engn, Lanzhou 730000, Peoples R China
[3] Gansu Prov Acad Tradit Chinese Med, Lanzhou 730000, Peoples R China
[4] Lanzhou Univ, Affiliated Hosp 1, Lanzhou 730000, Peoples R China
[5] Lanzhou Univ, Gansu Prov Key Lab Preclin Study New Tradit Chine, Lanzhou 730000, Peoples R China
关键词
different molecular weight range Hedysarum polybotrys polysaccharide; diabetes; oral glucose tolerant; hypoglycemic mechanism; hepatic glycogen; cell cytokines; insulin resistance; INDUCED DIABETIC-RATS; INSULIN-RESISTANCE; MEDICINAL-PLANTS; MECHANISMS; TISSUE; ALPHA; TUMOR; LIVER; MICE;
D O I
10.1139/Y09-098
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
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.
引用
收藏
页码:64 / 72
页数:9
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