α-黄柏烯对胰岛素抵抗性 3T3-L1 脂肪细胞的葡萄糖摄取和脂肪生成的影响:一种体外和硅学方法

Souprayen Seethalakshmi, Ravishankar Sarumathi, Chandrasekaran Sankaranarayanan
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摘要

目的:本研究旨在探讨薄荷、姜黄、黑胡椒和肉桂精油中的单萜类化合物α-黄柏烯对胰岛素抵抗状态下脂肪细胞功能的影响。材料与方法材料与方法:将成熟的 3T3-L1 脂肪细胞暴露于高葡萄糖(25 mM)和 0.6 nm/L 胰岛素中 24 小时,使其转化为 IR-3T3-L1 脂肪细胞。将脂肪细胞分为:第一组:正常对照组;第二组:糖尿病对照组;第三组:用α-黄烷(65 µM)处理的糖尿病组;第四组:用罗格列酮(0.1 µM)处理的糖尿病组。测定了葡萄糖摄取试验、甘油三酯累积和甘油-3-磷酸脱氢酶的活性。使用 Pyrx 软件中的 Auto Dock vina(V. 4.0)进行对接研究,分析了 alpha-phellandrene 与 PPARγ 和 SREBP-1c 的结合亲和力。结果结果:结果:与正常对照组相比,糖尿病对照组的葡萄糖摄取量、甘油三酯累积量和甘油-3-卟啉脱氢酶活性均有所下降。65 µM剂量的α-黄柏烯可增加脂肪细胞的葡萄糖摄取量,提高甘油-3-磷酸酯活性和甘油三酯积累,其效果与标准药物罗格列酮相当。分子对接研究发现,α-黄柏烯与关键转录因子 PPARγ 和 SREBP-1c 有很高的结合亲和力,而 PPARγ 和 SREBP-1c 与脂肪生成和类固醇生成有关。结论结论这些结果表明,α-黄柏烯能积极调节脂肪细胞功能,改善 II 型糖尿病患者的血脂异常和高血糖。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effect of Alpha-Phellandrene on Glucose Uptake and Adipogenesis in Insulin Resistant 3T3-L1 Adipocytes: an in vitro and in silico Approach
Aim: Aim: The present study was designated to investigate the effect of alpha-phellandrene, a monoterpene presents in essential oils of mint, turmeric, black pepper, and cinnamon on adipocyte function under insulin resistant condition. Materials and Methods: Materials and Methods: Mature 3T3-L1 adipocytes were exposed to high glucose (25 mM) and 0.6 nm/L of insulin for 24 hr to convert to IR-3T3-L1 adipocytes. The adipocytes were grouped into group1: normal control, group 2: diabetic control, group 3: diabetic group treated with alpha-phellandrene (65 µM) and group 4: diabetic group treated with rosiglitazone (0.1 µM). Glucose uptake assay, triglyceride accumulation and the activity of glycerol-3-phosphate dehydrogenase were measured. The binding affinity of alpha-phellandrene with PPARγ and SREBP-1c were analysed by docking studies by using Auto Dock vina (V. 4.0) in Pyrx software. Results: Results: Glucose uptake, triglyceride accumulation and activity of glycerol-3-phopshate dehydrogenase were found to be decreased in diabetic control when control to normal control group. Alpha-phellandrene at dose of 65 µM increased glucose uptake, enhanced glycerol-3-phosphate activity and triglyceride accumulation in adipocytes which were found to be comparable with the standard drug rosiglitazone. A high binding affinity of alpha-phellandrene with key transcription factors, PPARγ and SREBP-1c which are associated with adipogenesis and steroidogenesis were observed in molecular docking studies. Conclusion: Conclusion: These results suggest that alpha-phellandrene positively regulates adipocyte function and ameliorate dyslipidaemia and hyperglycaemia in type II diabetes mellitus.
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