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Circulating leptin and insulin in obese patients with and without type 2 diabetes mellitus: Relation to ghrelin and oxidative stress

机译:有和没有肥胖的2型糖尿病患者的循环瘦素和胰岛素:与生长素释放肽和氧化应激的关系

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Aim: This case control study aimed to investigate relationship between appetite hormones (ghrelin and leptin) and body mass index (BMI), insulin and oxidative stress in simple obese and type 2 diabetes (T2DM) obese patients. Methods: Thirty healthy controls; 30 simple obese and 30 T2DM obese patients were enrolled. Demographic and clinical data of all participants were reported. Serum levels of fasting blood glucose (FBG), postprandial blood glucose (PBG), lipid peroxide (LPO) and nitric oxide (NO) were measured by chemical methods while, insulin, leptin and ghrelin by ELISA kits. Results: Serum levels of insulin, leptin, LPO were significantly higher while, ghrelin was significantly lower in simple obese and obese patients with diabetes versus controls. Insulin resistance was found in 76.67% simple obese and 93.33% obese patients with diabetes. Ghrelin showed a positive correlation with PBG in controls; but negative correlation with BMI in simple obese and with NO in obese patients with diabetes. Positive correlations were found between LPO and FBG, insulin, homeostasis model assessment of insulin resistance (HOMA-IR) and between leptin and FBG in obese patients with diabetes. Conclusions: Our results suggested that hyperinsulinemia and hyperleptinemia may be most important mechanisms in decreasing ghrelin and inducing oxidative stress in simple obese and T2DM obese patients.
机译:目的:本病例对照研究旨在研究单纯性肥胖和2型糖尿病(T2DM)肥胖患者的食欲激素(生长素释放肽和瘦素)与体重指数(BMI),胰岛素和氧化应激之间的关系。方法:三十名健康对照者。招募了30例单纯性肥胖和30例T2DM肥胖患者。报告了所有参与者的人口统计学和临床​​数据。通过化学方法测定血清的空腹血糖(FBG),餐后血糖(PBG),脂质过氧化物(LPO)和一氧化氮(NO)水平,并通过ELISA试剂盒测量胰岛素,瘦素和生长素释放肽。结果:与对照组相比,单纯性肥胖和肥胖糖尿病患者的血清胰岛素,瘦素,LPO水平显着升高,而生长素释放肽显着降低。在76.67%的单纯性肥胖患者和93.33%的肥胖糖尿病患者中发现了胰岛素抵抗。 Ghrelin在对照组中与PBG呈正相关。但单纯肥胖者与BMI呈负相关,而糖尿病肥胖者与NO呈负相关。肥胖糖尿病患者的LPO与FBG,胰岛素,胰岛素抵抗稳态模型评估(HOMA-IR)以及瘦素与FBG之间存在正相关。结论:我们的结果表明,高胰岛素血症和高瘦素血症可能是降低单纯性肥胖症和T2DM肥胖症患者生长素释放肽和诱导氧化应激的最重要机制。

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