槲皮素可以减少长期喂食高脂高糖饮食的2型糖尿病雄性Wistar大鼠的肥胖和血脂异常,但不能减少胰岛素抵抗

A. Abuzaid, M. Osman, A. Elkhawad
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引用次数: 2

摘要

目前尚不清楚Wistar大鼠中2型糖尿病(T2D)相关胰岛素抵抗的持续是否完全依赖于肥胖和血脂异常或其他因素。我们想要揭示槲皮素减轻肥胖和血脂异常是否足以治愈糖尿病Wistar大鼠的胰岛素抵抗。将90只雄性Wistar大鼠随机分为3个实验组(n=30):正常对照组(NC)饲喂高脂高糖饲料(HFHSD),糖尿病对照组(DC)饲喂高脂高糖饲料(HFHSD),糖尿病槲皮素处理组(QT)饲喂高脂高糖饲料(HFHSD),槲皮素灌胃(50 mg)。公斤bw.day-1。在第0、60和120天,每组10只大鼠测量体重指数(BMI)和腹围:胸围(AC:TC)比。然后对大鼠实施安乐死,并抽取空腹血样,用于定量血浆葡萄糖、三环甘油(TAG)、低密度脂蛋白胆固醇(LDL-cholesterol)、总胆固醇(total cholesterol)、c反应蛋白(CRP)和胰岛素浓度。测定胰岛素抵抗评分、相对胰腺重量(RPW, %)和朗格汉斯胰岛数。我们发现槲皮素在第120天使QT大鼠的BMI、AC:TC比值、RPW(%)和血脂异常正常化,并使朗格汉斯胰岛数量增加。在糖尿病DC大鼠中,AC:TC比值与高血糖呈正相关,与RPW(%)呈负相关。槲皮素降低了QT大鼠相对于NC大鼠的高胰岛素血症、胰岛素抵抗评分、高血糖和CRP,但未能使其恢复正常,提示T2D Wistar大鼠胰岛素抵抗的发病机制中有其他因素参与。我们的数据还表明AC:TC比值是Wistar大鼠肥胖诱导的T2D的预测因子。
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Quercetin Curtails Obesity and Dyslipidemia, but Not Insulin Resistance in Long-Term Type 2 Diabetic Male Wistar Rats Fed the High-Fat, High-Sucrose Diet
It is unclear whether the persistence of Type 2 Diabetes (T2D)-associated insulin resistance in Wistar rats is entirely dependent on obesity and dyslipidemia or other factors are involved. We wanted to reveal whether alleviation of obesity and dyslipidemia by quercetin would sufficiently cure the insulin resistance in diabetic Wistar rats. For this purpose, ninety, male Wistar rats were randomized into three experimental groups (n=30): Normal Control (NC) fed chow diet, Diabetic Control (DC) fed High-Fat, High- Sucrose Diet (HFHSD) and diabetic, Quercetin-Treated (QT) fed the HFHSD and gavaged with quercetin at 50 mg.kg-1 bw.day-1. On Days 0, 60 and 120, Body Mass Index (BMI) and Abdominal Circumference:Thoracic Circumference (AC:TC) ratio were measured on ten rats from each group. Rats were then euthanized and fasting blood samples were withdrawn and used to quantify plasma glucose, Triacyclglycerols (TAG), LDL-cholesterol, total cholesterol, C-Reactive Protein (CRP) and insulin concentrations. Insulin resistance score, Relative Pancreatic Weight (RPW, %) and number of islet of Langerhans were also determined. We show that quercetin normalized BMI, AC:TC ratio, RPW (%) and dyslipidemia, and enhanced the islets number of Langerhans in the QT rats on Day 120 relative to the NC rats. In the diabetic DC rats, AC:TC ratio correlated positively with hyperglycemia and negatively with RPW (%). Quercetin lowered, but failed to normalize hyperinsulinemia, insulin resistance score, hyperglycemia and CRP in the QT rats relative to the NC rats suggesting that other factors are involved in the insulin resistance pathogenesis in T2D Wistar rats. Our data also suggest that AC:TC ratio is a predictor of the obesity-induced T2D in Wistar rats.
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