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Title: | Gut microbes modulate the effects of the flavonoid quercetin on atherosclerosis | Authors: | Kasahara, Kazuyuki Kerby, Robert L. Aquino-Martinez, Ruben Evered, Abigail H. Cross, Tzu-Wen L. Everhart, Jessica Ulland, Tyler K. Kay, Colin D. Bolling, Bradley W. Bäckhed, Fredrik Rey, Federico E. |
Keywords: | Medicine, Health and Life Sciences | Issue Date: | 2025 | Source: | Kasahara, K., Kerby, R. L., Aquino-Martinez, R., Evered, A. H., Cross, T. L., Everhart, J., Ulland, T. K., Kay, C. D., Bolling, B. W., Bäckhed, F. & Rey, F. E. (2025). Gut microbes modulate the effects of the flavonoid quercetin on atherosclerosis. Npj Biofilms and Microbiomes, 11(1), 12-. https://dx.doi.org/10.1038/s41522-024-00626-1 | Project: | RS10/22 MOH-001379 |
Journal: | npj Biofilms and Microbiomes | Abstract: | Gut bacterial metabolism of dietary flavonoids results in the production of a variety of phenolic acids, whose contributions to health remain poorly understood. Here, we show that supplementation with the commonly consumed flavonoid quercetin impacted gut microbiome composition and resulted in a significant reduction in atherosclerosis burden in conventionally raised (ConvR) Apolipoprotein E (ApoE) knockout (KO) mice but not in germ-free (GF) ApoE KO mice. Metabolomic analysis revealed that consumption of quercetin significantly increased plasma levels of benzoylglutamic acid, 3,4 dihydroxybenzoic acid (3,4-DHBA) and its sulfate-conjugated form in ConvR mice, but not in GF mice supplemented with the flavonoid. Levels of these metabolites were negatively associated with atherosclerosis burden. Furthermore, we show that 3,4-DHBA prevented lipopolysaccharide (LPS)-induced decrease in transendothelial electrical resistance (TEER). These results suggest that the effects of quercetin on atherosclerosis are influenced by gut microbes and are potentially mediated by bacterial metabolites derived from the flavonoid. | URI: | https://hdl.handle.net/10356/184693 | ISSN: | 2055-5008 | DOI: | 10.1038/s41522-024-00626-1 | Schools: | Lee Kong Chian School of Medicine (LKCMedicine) | Rights: | © 2024 The Author(s). Open Access. This article is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License, which permits any non-commercial use, sharing, 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 licence, and indicate if you modified the licensed material. You do not have permission under this licence to share adapted material derived from this article or parts of it. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/bync-nd/4.0/. | Fulltext Permission: | open | Fulltext Availability: | With Fulltext |
Appears in Collections: | LKCMedicine Journal Articles |
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s41522-024-00626-1.pdf | 1.39 MB | Adobe PDF | View/Open |
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