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双黄酮的抗氧化潜力通过调节高脂肪饮食/链脲佐菌素诱导的糖尿病大鼠的碳水化合物代谢酶来减轻高血糖。

Antioxidant potential of biflavonoid attenuates hyperglycemia by modulating the carbohydrate metabolic enzymes in high fat diet/streptozotocin induced diabetic rats.

机构信息

Department of Medical Biochemistry, University of Madras, Chennai, India.

Department of Biochemistry, Saveetha Dental College & Hospital, Saveetha Institute of Medical &Technical Sciences, Saveetha University, Chennai, India.

出版信息

Redox Rep. 2020 Dec;25(1):1-10. doi: 10.1080/13510002.2020.1722914.

Abstract

The present study was to isolate the biflavonoid (a bimolecular kaemferol structured molecule) and test its efficacy on oxidative stress and carbohydrate metabolic key enzymes in control and high fat diet and streptozotocin -induced diabetic rats. Type 2 diabetes was induced in male albino wistar rats by feeding them with high fat diet comprising of 84.3% standard laboratory chow, 5% lard, 10% yolk powder, cholesterol 0.2%, and 0.5% bile salt for 2 weeks. After 2 weeks, the animals were kept in an overnight fast and injected with low dose of streptozotocin (35 mg/kg, dissolved in 0.1 M sodium citrate buffer, pH 4.5). At the end of the experimental period, diabetic control rats showed significant increase in plasma glucose, homeostatic model assessment of insulin resistance (HOMA-IR), glycosylated hemoglobin (HbA1c) with concomitant decrease in plasma insulin, total hemoglobin and body weight. The activities of key enzymes of carbohydrate metabolism, lipid peroxidation markers, antioxidant enzymes, glycogen content and glycogen synthase and glycogen phosphorylase were also altered in diabetic rats. Oral administration of biflavonoid to diabetic rats significantly ameliorated all the biochemical alterations to near normal levels. The effect produced by the biflavonoid on various parameters was comparable to that of metformin.

摘要

本研究旨在分离双黄酮(一种由二分子山柰酚构成的分子)并测试其对正常饮食和高脂肪饮食以及链脲佐菌素诱导的糖尿病大鼠氧化应激和碳水化合物代谢关键酶的疗效。雄性白化 Wistar 大鼠通过喂食包含 84.3%标准实验室饲料、5%猪油、10%蛋黄粉、0.2%胆固醇和 0.5%胆盐的高脂肪饮食 2 周来诱导 2 型糖尿病。2 周后,动物禁食过夜,并注射低剂量链脲佐菌素(35mg/kg,溶于 0.1M 柠檬酸钠缓冲液,pH4.5)。在实验期末,糖尿病对照大鼠的血浆葡萄糖、稳态模型评估的胰岛素抵抗(HOMA-IR)、糖化血红蛋白(HbA1c)显著增加,同时血浆胰岛素、总血红蛋白和体重下降。糖尿病大鼠碳水化合物代谢关键酶、脂质过氧化标志物、抗氧化酶、糖原含量和糖原合酶及糖原磷酸化酶的活性也发生改变。双黄酮口服给予糖尿病大鼠可显著改善所有生化改变,接近正常水平。双黄酮对各种参数的作用与二甲双胍相当。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3388/7034448/98b1d24ade38/YRER_A_1722914_F0001_OB.jpg

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