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仙人掌多糖新成分的降血糖作用。

Antidiabetic effect of a newly identified component of Opuntia dillenii polysaccharides.

机构信息

College of Life Science and Technology, Zhanjiang Normal University, Zhanjiang, Guangdong, China.

出版信息

Phytomedicine. 2011 Jun 15;18(8-9):661-8. doi: 10.1016/j.phymed.2011.01.001. Epub 2011 Feb 5.

DOI:10.1016/j.phymed.2011.01.001
PMID:21300531
Abstract

The aim of this study was to determine the most effective hypoglycemic component of polysaccharides from Opuntia dillenii Haw. by preliminary screening and to specifically study the antidiabetic effects of O. dillenii polysaccharide (ODP)-Ia in mice with streptozotocin (STZ)-induced diabetes. Three kinds of ODPs - ODP-Ia, ODP-Ib, and ODP-II' - were isolated by using an ultrasonic extraction method and diethylaminoethyl (DEAE)-Sepharose fast-flow column chromatography. The mice were administered ODPs for 3 weeks. Gavage administration of ODP-Ia significantly decreased (P<0.05) their intake of food and water; the fasting levels of blood glucose (BG), total cholesterol (TC), triglycerides (TGs), plasma urea nitrogen (PUN), and malondialdehyde (MDA); and the activity of glucose-6-phosphatase (G-6-Pase). In contrast, it significantly increased (P<0.05) the body weights, hepatic glycogen (HG) levels, high-density lipoprotein cholesterol (HDL-C) levels, and the hepatic superoxide dismutase (SOD) and glutathione peroxidase (GSH-Px) activity in diabetic mice. However, ODP-Ia did not significantly increase insulin levels in the mice with STZ-induced diabetes. We propose that ODP-Ia exerts its antihyperglycemic effect by protecting the liver from peroxidation damage and by maintaining tissue function, thereby improving the sensitivity and response of target cells in diabetic mice to insulin.

摘要

本研究旨在通过初步筛选确定仙人掌多糖中降血糖的有效成分,并专门研究仙人掌多糖(ODP)-Ia 在链脲佐菌素(STZ)诱导的糖尿病小鼠中的降血糖作用。采用超声提取法和二乙氨基乙基(DEAE)-Sepharose 快速流动柱色谱法分离三种 ODP-ODP-Ia、ODP-Ib 和 ODP-II'。将小鼠给予 ODP 治疗 3 周。ODP-Ia 灌胃给药可显著降低(P<0.05)其食物和水的摄入量;空腹血糖(BG)、总胆固醇(TC)、甘油三酯(TGs)、血浆尿素氮(PUN)和丙二醛(MDA)水平;以及葡萄糖-6-磷酸酶(G-6-Pase)的活性。相反,它可显著增加(P<0.05)糖尿病小鼠的体重、肝糖原(HG)水平、高密度脂蛋白胆固醇(HDL-C)水平以及肝超氧化物歧化酶(SOD)和谷胱甘肽过氧化物酶(GSH-Px)的活性。然而,ODP-Ia 并未显著增加 STZ 诱导的糖尿病小鼠的胰岛素水平。我们提出,ODP-Ia 通过保护肝脏免受过氧化损伤和维持组织功能来发挥其降血糖作用,从而提高糖尿病小鼠靶细胞对胰岛素的敏感性和反应性。

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