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Molecular Mechanism of Resveratrol’s Lipid Membrane Protection
Resveratrol, a natural compound found in red wine and various vegetables, has drawn increasing interest due to its reported benefit in cardiovascular protection, neurodegenerative disorders, and cancer therapy. The mechanism by which resveratrol exerts such pleiotropic effects remains unclear. It re...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5785473/ https://www.ncbi.nlm.nih.gov/pubmed/29371621 http://dx.doi.org/10.1038/s41598-017-18943-1 |
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author | Fei, Qinqin Kent, David Botello-Smith, Wesley M. Nur, Fariah Nur, Saadia Alsamarah, Abdelaziz Chatterjee, Payal Lambros, Maria Luo, Yun |
author_facet | Fei, Qinqin Kent, David Botello-Smith, Wesley M. Nur, Fariah Nur, Saadia Alsamarah, Abdelaziz Chatterjee, Payal Lambros, Maria Luo, Yun |
author_sort | Fei, Qinqin |
collection | PubMed |
description | Resveratrol, a natural compound found in red wine and various vegetables, has drawn increasing interest due to its reported benefit in cardiovascular protection, neurodegenerative disorders, and cancer therapy. The mechanism by which resveratrol exerts such pleiotropic effects remains unclear. It remains as one of the most discussed polyphenol compounds in the debating "French Paradox". In this study, using molecular dynamics simulations of dipalmitoyl phosphatidylcholine (DPPC) bilayer with resveratrol, we generated a free energy map of resveratrol’s location and orientation of inside the lipid bilayer. We found that resveratrol increases the surface area per lipid and decreases membrane thickness, which is the opposite effect of the well-studied cholesterol on liquid phase DPPC. Most importantly, based on the simulation observation that resveratrol has a high probability of forming hydrogen bonds with sn-1 and sn-2 ester groups, we discovered a new mechanism using experimental approach, in which resveratrol protects both sn-1 and sn-2 ester bonds of DPPC and distearoyl phosphatidylcholine (DSPC) from phospholipase A1 (PLA1) and phospholipase A2 (PLA2) cleavage. Our study elucidates the new molecular mechanism of potential health benefits of resveratrol and possibly other similar polyphenols and provides a new paradigm for drug design based on resveratrol and its analogs. |
format | Online Article Text |
id | pubmed-5785473 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-57854732018-02-07 Molecular Mechanism of Resveratrol’s Lipid Membrane Protection Fei, Qinqin Kent, David Botello-Smith, Wesley M. Nur, Fariah Nur, Saadia Alsamarah, Abdelaziz Chatterjee, Payal Lambros, Maria Luo, Yun Sci Rep Article Resveratrol, a natural compound found in red wine and various vegetables, has drawn increasing interest due to its reported benefit in cardiovascular protection, neurodegenerative disorders, and cancer therapy. The mechanism by which resveratrol exerts such pleiotropic effects remains unclear. It remains as one of the most discussed polyphenol compounds in the debating "French Paradox". In this study, using molecular dynamics simulations of dipalmitoyl phosphatidylcholine (DPPC) bilayer with resveratrol, we generated a free energy map of resveratrol’s location and orientation of inside the lipid bilayer. We found that resveratrol increases the surface area per lipid and decreases membrane thickness, which is the opposite effect of the well-studied cholesterol on liquid phase DPPC. Most importantly, based on the simulation observation that resveratrol has a high probability of forming hydrogen bonds with sn-1 and sn-2 ester groups, we discovered a new mechanism using experimental approach, in which resveratrol protects both sn-1 and sn-2 ester bonds of DPPC and distearoyl phosphatidylcholine (DSPC) from phospholipase A1 (PLA1) and phospholipase A2 (PLA2) cleavage. Our study elucidates the new molecular mechanism of potential health benefits of resveratrol and possibly other similar polyphenols and provides a new paradigm for drug design based on resveratrol and its analogs. Nature Publishing Group UK 2018-01-25 /pmc/articles/PMC5785473/ /pubmed/29371621 http://dx.doi.org/10.1038/s41598-017-18943-1 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Fei, Qinqin Kent, David Botello-Smith, Wesley M. Nur, Fariah Nur, Saadia Alsamarah, Abdelaziz Chatterjee, Payal Lambros, Maria Luo, Yun Molecular Mechanism of Resveratrol’s Lipid Membrane Protection |
title | Molecular Mechanism of Resveratrol’s Lipid Membrane Protection |
title_full | Molecular Mechanism of Resveratrol’s Lipid Membrane Protection |
title_fullStr | Molecular Mechanism of Resveratrol’s Lipid Membrane Protection |
title_full_unstemmed | Molecular Mechanism of Resveratrol’s Lipid Membrane Protection |
title_short | Molecular Mechanism of Resveratrol’s Lipid Membrane Protection |
title_sort | molecular mechanism of resveratrol’s lipid membrane protection |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5785473/ https://www.ncbi.nlm.nih.gov/pubmed/29371621 http://dx.doi.org/10.1038/s41598-017-18943-1 |
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