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利用分子对接技术探索茶的降血糖化学成分及作用机制

Exploring the Antihyperglycemic Chemical Composition and Mechanisms of Tea Using Molecular Docking.

作者信息

Sun Yue, Wang Lufei, Shaughnessy Lily K, Lin Yan, Xu Qingliang, Shi Xueping, Zhang Liang, Yu Rilei, Xiao Hang, Wan Xiaochun, Wu Xian

机构信息

State Key Laboratory of Tea Plant Biology and Utilization, Anhui Engineering Laboratory for Agro-Products Processing, Anhui Agricultural University, Hefei 230036, China.

MOE Key Laboratory of Contemporary Anthropology, B & R International Joint Laboratory of Eurasian Anthropology, School of Life Sciences, Fudan University, Shanghai 200438, China.

出版信息

Evid Based Complement Alternat Med. 2020 Dec 2;2020:8871088. doi: 10.1155/2020/8871088. eCollection 2020.

Abstract

Tea, a widely consumed beverage, has long been utilized for promoting human health with a close correlation to hyperglycemia. The Tea Metabolome Database (TMDB), the most complete and comprehensive curated collection of tea compounds data containing 1271 identified small molecule compounds from the tea plant (), was established previously by our research team. More recently, our studies have found that various tea types possess an antihyperglycemic effect in mice. However, the bioactive ingredients from tea have potential antihyperglycemic activity and their underlying molecular mechanisms remain unclear. In this study, we used a molecular docking approach to investigate the potential interactions between a selected 747 constituents contained in tea and 11 key protein targets of clinical antihyperglycemic drugs. According to our results, the main antihyperglycemic targets of tea composition were consistent with those of the drug rosiglitazone. The screening results showed that GCG, ECG3'Me, TMDB-01443, and CG had great target binding capacity. The results indicated that these chemicals of tea might affect hyperglycemia by acting on protein targets of rosiglitazone.

摘要

茶是一种广泛饮用的饮品,长期以来一直被用于促进人类健康,且与高血糖密切相关。茶代谢组数据库(TMDB)是我们的研究团队之前建立的最完整、最全面的茶化合物数据精选集合,其中包含从茶树中鉴定出的1271种小分子化合物。最近,我们的研究发现,不同类型的茶对小鼠具有降血糖作用。然而,茶中的生物活性成分具有潜在的降血糖活性,但其潜在的分子机制仍不清楚。在本研究中,我们使用分子对接方法来研究茶中选定的747种成分与临床降血糖药物的11个关键蛋白质靶点之间的潜在相互作用。根据我们的结果,茶成分的主要降血糖靶点与罗格列酮药物的靶点一致。筛选结果表明,GCG、ECG3'Me、TMDB-01443和CG具有很强的靶点结合能力。结果表明,茶中的这些化学物质可能通过作用于罗格列酮的蛋白质靶点来影响高血糖。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af84/7725569/66cc4cd2e781/ECAM2020-8871088.001.jpg

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