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操兰洁, 诸夔妞, 蒋翠花, 乔丹·甘恩, 车镇涛, 张健, 殷志琦. 泽泻提取物对STZ糖尿病大鼠的干预作用[J]. 中国药科大学学报, 2017, 48(5): 601-608. DOI: 10.11665/j.issn.1000-5048.20170516
引用本文: 操兰洁, 诸夔妞, 蒋翠花, 乔丹·甘恩, 车镇涛, 张健, 殷志琦. 泽泻提取物对STZ糖尿病大鼠的干预作用[J]. 中国药科大学学报, 2017, 48(5): 601-608. DOI: 10.11665/j.issn.1000-5048.20170516
CAO Lanjie, ZHU Kuiniu, JIANG Cuihua, GUNN ·Jordan, CHE Chun-Tao, ZHANG Jian, YIN Zhiqi. Intervention effects of the extract of Alismatis Rhizoma on streptozotocin-induced type 2 diabetic rats[J]. Journal of China Pharmaceutical University, 2017, 48(5): 601-608. DOI: 10.11665/j.issn.1000-5048.20170516
Citation: CAO Lanjie, ZHU Kuiniu, JIANG Cuihua, GUNN ·Jordan, CHE Chun-Tao, ZHANG Jian, YIN Zhiqi. Intervention effects of the extract of Alismatis Rhizoma on streptozotocin-induced type 2 diabetic rats[J]. Journal of China Pharmaceutical University, 2017, 48(5): 601-608. DOI: 10.11665/j.issn.1000-5048.20170516

泽泻提取物对STZ糖尿病大鼠的干预作用

Intervention effects of the extract of Alismatis Rhizoma on streptozotocin-induced type 2 diabetic rats

  • 摘要: 为评价泽泻乙酸乙酯部位对2型糖尿病的降血糖作用及其机制,采用高脂高糖饲料喂养大鼠4周后再腹腔注射小剂量链尿佐菌素(STZ)的方法,建立2型糖尿病大鼠模型。将糖尿病大鼠随机分为模型组、泽泻乙酸乙酯部位组(AREEA,20,50,100 mg/kg)、二甲双胍组(100 mg/kg)。连续给药4周后进行葡萄糖耐量和胰岛素耐量实验。于末次给药后禁食12 h,采血测定大鼠空腹血糖(GLU)、糖化血红蛋白(HbA1c)、胰岛素(Ins)以及胆固醇(TC)、三酰甘油(TG)、高密度脂蛋白(HDL-C)、低密度脂蛋白(LDL-C)、丙二醛(MDA)、超氧化物歧化酶(SOD)、谷胱甘肽过氧化物酶(GSH-Px)、肿瘤坏死因子-α(TNF-α)、白介素-6(IL-6)含量,脂肪组织中胰岛素信号通路IRS-1和Akt的磷酸化水平及胰脏的病理变化。结果显示,给药组大鼠的空腹血糖有明显降低(P<;0.05);100 mg/kg组显著降低血清GLU、HbA1c、TC、TG、MDA、TNF-α、IL-6(P<;0.05);明显升高SOD、GSH-Px(P<;0.05)。这些结果提示泽泻乙酸乙酯部位可有效调节体内糖、脂代谢,对2型糖尿病有一定治疗作用。

     

    Abstract: To investigate the hypoglycemic effects of ethyl acetate extract of Alismatis Rhizoma(AREEA)on type 2 diabetes mellitus, the model of type 2 diabetic rats was induced by high-fat diet feeding for 4 weeks and then intraperitoneal injection of a low dose of streptozotoin(STZ). Rats without the above-mentioned treatment were selected as the normal control group. The diabetic rats were randomly divided into 5 groups: the model control group, low doses(20 mg/kg), medium doses(50 mg/kg), high doses(100 mg/kg)of AREEA groups and positive control-metformin group(100 mg/kg). After four weeks, oral glucose tolerance test(OGTT)and insulin tolerance test(ITT)were performed, respectively. 12 hours after the last administration, the levels of serum glucose, glycated hemoglobin(HbA1c), insulin(Ins), total cholesterol(TC), triglyceride(TG), high density lipoprotein(HDL-C), low density lipoprotein(LDL-C), superoxide dismutase(SOD), malondialdehyde(MDA), glutathione(GSH-Px), tumor necrosis factor-α(TNF-α), interleukin-6(IL-6), insulin-mediated tyrosine of IRS-1 and Akt phosphorylation in adipose tissue were determined. In addition, the pathological changes of pancreas were examined. After administration for 4 weeks, all doses of AREEA significantly reduced the fasting blood glucose of type 2 diabetic rats(P< 0. 05). In the high doses group of AREEA, the levels of GLU, HbA1c, TC, TG, MDA, TNF-α and IL-6 in serum were decreased significantly, and the levels of SOD and GSH-Px were increased(P< 0. 05). These results suggest that AREEA has the therapeutic effect on type 2 diabetes-related symptoms by metabolic regulation of glucose and lipids.

     

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