Kursi Ziyabet对糖尿病大鼠模型影响的实验研究

Alimjan Parhat, H. Huojiaaihemaiti, Nabijan Mohammadturusn, M. Nurahmat
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摘要

目的:观察苦参紫珠贝特片对糖尿病大鼠模型的高血糖作用。方法:将58只雄性SD大鼠随机分为6组。除正常组外,其余均通过注射链脲佐菌素转化为实验性糖尿病大鼠模型。采用大鼠实验模型,通过相应试剂盒测定氧化应激相关因子和脂质代谢指标水平,从体重、食物和水的摄入量、空腹血糖及相关参数等方面评价紫珠贝特的高血糖作用及其机制。结果:与模型组相比,Ziyabet片灌胃3-6周后,体重显著增加([公式:见正文]),而同一时间段内的摄水量显著减少([公式,见正文]])。Ziyabet片([配方:见正文])的高剂量也降低了食物摄入量和空腹血糖水平。Ziyabet组的胰腺MDA含量与模型组相比没有显著差异([公式:见正文]),而高剂量KZ组的SOD水平显著升高([公式,见文本])。与模型组相比,高剂量KZ组的血清胰岛素和游离脂肪酸水平也有所下降([公式:见正文])。结论:紫珠贝特片对糖尿病大鼠模型具有保护作用。
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Experimental study on the effects of Kursi Ziyabet on the rat model of diabetes mellitus
Objective: To evaluate the hyperglycemic effects of Kursi Ziyabet (KZ) tablets on the rat models of diabetes mellitus. Methods: In total, 58 male SD rats were assigned randomly to six groups. All except the normal group were transformed into experimental diabetes mellitus rat models by injecting streptozocin. The hyperglycemic effect and the mechanism of Ziyabet were evaluated by body weight, food and water intake, fasting blood sugar, and related parameters by measuring the oxidative stress-related factors and lipid metabolism indicator level by the corresponding kits using the rat experimental models. Results: Compared with the model group, body weight markedly increased after 3–6 weeks of intragastric administration of Ziyabet tablets ([Formula: see text]), while the water intake significantly decreased in the same period of time ([Formula: see text]). Food intake and fasting blood sugar level also decreased with the high dosage of Ziyabet tablets ([Formula: see text]). There is no significant difference in pancreas’ MDA content of the Ziyabet groups when compared to the model group ([Formula: see text]), while significant increase in SOD level was observed in high-dosage KZ group ([Formula: see text]). The blood serum insulin and free fatty acid level also decreased in the high-dosage KZ group compared with the model group ([Formula: see text]). Conclusion: We conclude that Ziyabet tablets demonstrated protective effects on the diabetic rat models.
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