咖啡因与α-脂酸复合物预防链脲佐菌素诱导的大鼠糖尿病的实验研究

Q4 Medicine
K. R. Abidin, A. Meliala, Sri Lestari Sulistyo Rini
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引用次数: 0

摘要

目的:本研究旨在探讨咖啡因和α硫辛酸(ALA)对链脲佐菌素(STZ)诱导的糖尿病大鼠慢性高血糖氧化应激的联合作用(体内法和体外法)。材料与方法:本实验通过分子对接研究了咖啡因和ALA对胰岛素受体和谷胱甘肽过氧化物酶-1 (GPx-1)酶的相互作用。雄性Wistar大鼠采用准实验研究设计,仅设后测组和对照组(体内)。本研究测量了25只大鼠6周诱导后的体重、空腹血糖、丙二醛(MDA)和GPx-1酶的最终结果。结果:分子对接发现咖啡因与GPx-1的相互作用由-5,06 kcal/mol的能量键、氢键和疏水键组成。结果表明,ALA与GPx-1的相互作用具有-5.16 kcal/mol的能键、氢键和疏水性。然而,与糖尿病大鼠相比,含ala咖啡因的糖尿病大鼠的体重、空腹血糖、MDA和GPx-1水平均无显著差异。结论:咖啡因和ALA有可能激活GPx-1酶(在硅研究中)。然而,与没有额外诱导的糖尿病大鼠相比,使用咖啡因和ALA组合导致空腹血糖和氧化应激条件没有显着差异(体内研究)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effects of Caffeine mixed with Alpha Lipoic Acid in Preventing Streptozotocin-induced Diabetes in Rats: In Silico and In vivo Study
Objective: This study aimed to investigate the combined effects of caffeine and Alpha Lipoic Acid (ALA) on oxidative stress, due to chronic hyperglycemia, in a model of diabetic rats induced with streptozotocin (STZ) (in silico and in vivo approaches). Material and Methods: This In silico study investigated the interaction between caffeine and ALA against insulin receptors and enzymes of Glutathione Peroksidase-1 (GPx-1), with molecular docking. Male, Wistar rats were included using a quasi-experimental research design, with post-test only and a control group (in vivo). This study measured the end result of a 6-week-induction on body weight, fasting blood glucose, Malondialdehyde (MDA) and GPx-1 enzyme from 25 rats. Results: Molecular docking found the interactions of caffeine and GPx-1 consisting of an energy bond of -5,06 kcal/mol, hydrogen and hydrophobic bond. Additionally, it showed the interaction of ALA and GPx-1 containing an energy bond of -5.16 kcal/mol, hydrogen bonding and hydrophobicity. However, there were no significant difference in body weight, fasting blood glucose, MDA and GPx-1 levels of the ALA-caffeinated diabetic rats compared to diabetic rats.Conclusion: Caffeine and ALA have the potential to activate GPx-1 enzymes (in silico study). However, the use of a caffeine and ALA combination resulted in no significant difference in fasting blood glucose and oxidative stress conditions when compared to diabetic rats without additional induction (in vivo study). 
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CiteScore
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