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通过分子对接探究不同加工方法的茶多酚与抗肥胖及与氧化三甲胺生成相关酶的结合机制。

Probing the binding mechanism of tea polyphenols from different processing methods to anti-obesity and TMAO production-related enzymes through molecular docking.

作者信息

Wang Zhuo, Chen Bin, Zhao Xinyi, Li Shanshan, Fang Zhengfeng, Liu Yuntao, Zeng Zhen, Li Cheng, Chen Hong

机构信息

College of Food Science, Sichuan Agricultural University, Yaan, Sichuan 625014, China.

出版信息

Food Chem X. 2023 Dec 14;21:101053. doi: 10.1016/j.fochx.2023.101053. eCollection 2024 Mar 30.

Abstract

Tea polyphenols possess anti-obesity properties and reduce TMAO levels. However, the variability of tea polyphenols under different processing methods and their preventive efficacy requires further exploration. This study systematically evaluated the antioxidant, hypoglycemic, and hypolipotropic enzyme capacities of GT, YT and DT through UPLC-ESI-MS/MS analysis of catechin profiles. OPLS, correlation analysis, and molecular docking were employed to investigate the compounds and inhibitory mechanisms targeting hypoglycemic, hypolipidemic, and TMAO-producing enzymes. GT exhibited significantly lower IC values for biological activity and higher catechins contents compared to YT and DT ( < 0.05). Strong positive correlations were observed between EGCG, CG, and ECG and biological activities (r ≥ 7.4,  < 0.001). Molecular docking results highlighted the establishment of stable hydrogen bonds and hydrophobic interactions between EGCG, CG, ECG, and the receptor. These findings contribute novel insights into the mechanisms by which tea polyphenols prevent obesity and inhibit TMAO production.

摘要

茶多酚具有抗肥胖特性并能降低氧化三甲胺(TMAO)水平。然而,不同加工方法下茶多酚的变异性及其预防功效仍需进一步探索。本研究通过对儿茶素谱进行超高效液相色谱-电喷雾串联质谱(UPLC-ESI-MS/MS)分析,系统评估了绿茶(GT)、黄茶(YT)和黑茶(DT)的抗氧化、降血糖和降血脂酶能力。采用正交偏最小二乘法判别分析(OPLS)、相关性分析和分子对接来研究针对降血糖、降血脂和产生TMAO的酶的化合物及抑制机制。与YT和DT相比,GT的生物活性IC值显著更低,儿茶素含量更高(P < 0.05)。表没食子儿茶素没食子酸酯(EGCG)、儿茶素没食子酸酯(CG)和表儿茶素没食子酸酯(ECG)与生物活性之间存在强正相关(r ≥ 7.4,P < 0.001)。分子对接结果突出显示了EGCG、CG、ECG与受体之间形成了稳定的氢键和疏水相互作用。这些发现为茶多酚预防肥胖和抑制TMAO产生的机制提供了新的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f0b/10767370/a237e8910271/gr1.jpg

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