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白藜芦醇能否影响11β-羟基类固醇脱氢酶1型的活性?一项计算机模拟与体内实验相结合的研究。

Can Resveratrol Influence the Activity of 11β-Hydroxysteroid Dehydrogenase Type 1? A Combined In Silico and In Vivo Study.

作者信息

Novak Jurica, Tseilikman Vadim E, Tseilikman Olga B, Lazuko Svetlana S, Belyeva Lyudmila E, Rahmani Azam, Fedotova Julia

机构信息

Department of Biotechnology, University of Rijeka, 51000 Rijeka, Croatia.

Center for Artificial Intelligence and Cyber Security, University of Rijeka, 51000 Rijeka, Croatia.

出版信息

Pharmaceuticals (Basel). 2023 Feb 7;16(2):251. doi: 10.3390/ph16020251.

DOI:10.3390/ph16020251
PMID:37259398
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9960807/
Abstract

The enzyme 11β-hydroxysteroid dehydrogenase type 1 (11β-HSD-1) is an NADPH-dependent reductase, responsible for the activation of cortisol by reducing cortisone. Resveratrol (RES), a type of natural polyphenol, is reported to be able to slow the progression of cancer and cardiovascular disease and improve the health of mice on a high-calorie diet. In this article, we applied molecular docking and molecular dynamics simulations to investigate the possibility of binding RES to 11β-HSD-1. The 11β-HSD-1:RES complex is stable on the μs time scale, and backbone RMSD-based clustering identified three conformations. Special attention was paid to the interaction pattern between the ligand and the target molecule, revealing hydrogen bonds between the hydroxyl group of RES and Thr124, as well as hydrophobic interactions responsible for the binding. In vivo studies demonstrated the ability of resveratrol at a dose of 40 mg/kg to reduce 11β-HSD-1 activity in the liver of rats under conditions of experimental post-traumatic stress disorder (PTSD), as well as in non-stressed animals. In both cases, the resveratrol-induced reduction in 11β-HSD-1 activity was accompanied by an increase in plasma corticosterone levels and a decrease in anxiety levels in the plus maze test.

摘要

11β-羟类固醇脱氢酶1型(11β-HSD-1)是一种依赖烟酰胺腺嘌呤二核苷酸磷酸(NADPH)的还原酶,负责通过将可的松还原为皮质醇来激活皮质醇。白藜芦醇(RES)是一种天然多酚,据报道能够减缓癌症和心血管疾病的进展,并改善高热量饮食小鼠的健康状况。在本文中,我们应用分子对接和分子动力学模拟来研究白藜芦醇与11β-HSD-1结合的可能性。11β-HSD-1:RES复合物在微秒时间尺度上是稳定的,基于主链均方根偏差(RMSD)的聚类确定了三种构象。我们特别关注配体与靶分子之间的相互作用模式,发现白藜芦醇的羟基与苏氨酸124之间存在氢键,以及负责结合的疏水相互作用。体内研究表明,在实验性创伤后应激障碍(PTSD)条件下,40mg/kg剂量的白藜芦醇能够降低大鼠肝脏中的11β-HSD-1活性,在非应激动物中也是如此。在这两种情况下,白藜芦醇诱导的11β-HSD-1活性降低伴随着血浆皮质酮水平的升高和加迷宫试验中焦虑水平的降低。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/622f/9960807/c46062448da7/pharmaceuticals-16-00251-g008.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/622f/9960807/30f42b22b4e8/pharmaceuticals-16-00251-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/622f/9960807/3860e726bbbd/pharmaceuticals-16-00251-g006.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/622f/9960807/c46062448da7/pharmaceuticals-16-00251-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/622f/9960807/1d77107be5fe/pharmaceuticals-16-00251-sch001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/622f/9960807/01eec9cbb54c/pharmaceuticals-16-00251-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/622f/9960807/6cf499a4c861/pharmaceuticals-16-00251-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/622f/9960807/41f41e9ce3bb/pharmaceuticals-16-00251-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/622f/9960807/9417cf667757/pharmaceuticals-16-00251-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/622f/9960807/30f42b22b4e8/pharmaceuticals-16-00251-g005.jpg
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