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Effect of urolithin A on the improvement of vascular endothelial function depends on the gut microbiota

BACKGROUND: Urolithin A (UA) is a metabolite produced by gut microbiota from ingested ellagic acid. Although the effect of ellagic acid intake on vascular endothelial function (VEF) improvement has been reported, the effect of UA intake on VEF improvement remains obscure. In addition, UA has been re...

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Autores principales: Nishimoto, Yuichiro, Fujisawa, Kota, Ukawa, Yuichi, Kudoh, Masatake, Funahashi, Kazuki, Kishimoto, Yoshimi, Fukuda, Shinji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9854132/
https://www.ncbi.nlm.nih.gov/pubmed/36687672
http://dx.doi.org/10.3389/fnut.2022.1077534
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author Nishimoto, Yuichiro
Fujisawa, Kota
Ukawa, Yuichi
Kudoh, Masatake
Funahashi, Kazuki
Kishimoto, Yoshimi
Fukuda, Shinji
author_facet Nishimoto, Yuichiro
Fujisawa, Kota
Ukawa, Yuichi
Kudoh, Masatake
Funahashi, Kazuki
Kishimoto, Yoshimi
Fukuda, Shinji
author_sort Nishimoto, Yuichiro
collection PubMed
description BACKGROUND: Urolithin A (UA) is a metabolite produced by gut microbiota from ingested ellagic acid. Although the effect of ellagic acid intake on vascular endothelial function (VEF) improvement has been reported, the effect of UA intake on VEF improvement remains obscure. In addition, UA has been reported to improve the intestinal barrier function, and UA may have improved VEF by gut microbiome alteration. OBJECTIVE: In this study, we conducted a clinical trial to explore and analyze the effects of UA intake on vascular endothelial function (VEF) and characteristics of the intestinal environment, such as gut microbiome profiling and organic acid composition. METHODS: A placebo-controlled, randomized, double-blinded, parallel group trial was conducted on participants who could metabolize small amounts of UA from ellagic acid (non-UA producers) and had relatively poor VEF. VEF was assessed using the flow-mediated vasodilatation (FMD) score. Participants were administered placebo, UA 10 mg/day, or UA 50 mg/day for 12 weeks. FMD was measured and fecal samples were collected at 0, 4, 8, and 12 weeks of treatment. Gut microbiome analysis and organic acid level measurements were performed to evaluate the effects of UA intake on the intestinal environment. This clinical trial is publicly registered at the UMIN-CTR, trial number: UMIN000042014. RESULTS: The gut microbiota of the UA 50 mg/day group showed a significant increase in alpha diversity (Faith’s phylogenetic diversity). Four and nine microbial genera were significantly altered in the UA 10 mg/day and UA 50 mg/day groups, respectively (p < 0.05, not corrected). Participants whose FMD scores improved with UA intake had poor baseline FMD values as well as a low Bacillota/Bacteroidota ratio. CONCLUSION: Urolithin A intake alters the gut microbiota and improves their alpha diversity. In addition, the effect of UA on VEF correlated with the individual gut microbiota. Our results have practical implications for a new approach to providing healthcare that focuses on intestinal environment-based diet therapy.
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spelling pubmed-98541322023-01-21 Effect of urolithin A on the improvement of vascular endothelial function depends on the gut microbiota Nishimoto, Yuichiro Fujisawa, Kota Ukawa, Yuichi Kudoh, Masatake Funahashi, Kazuki Kishimoto, Yoshimi Fukuda, Shinji Front Nutr Nutrition BACKGROUND: Urolithin A (UA) is a metabolite produced by gut microbiota from ingested ellagic acid. Although the effect of ellagic acid intake on vascular endothelial function (VEF) improvement has been reported, the effect of UA intake on VEF improvement remains obscure. In addition, UA has been reported to improve the intestinal barrier function, and UA may have improved VEF by gut microbiome alteration. OBJECTIVE: In this study, we conducted a clinical trial to explore and analyze the effects of UA intake on vascular endothelial function (VEF) and characteristics of the intestinal environment, such as gut microbiome profiling and organic acid composition. METHODS: A placebo-controlled, randomized, double-blinded, parallel group trial was conducted on participants who could metabolize small amounts of UA from ellagic acid (non-UA producers) and had relatively poor VEF. VEF was assessed using the flow-mediated vasodilatation (FMD) score. Participants were administered placebo, UA 10 mg/day, or UA 50 mg/day for 12 weeks. FMD was measured and fecal samples were collected at 0, 4, 8, and 12 weeks of treatment. Gut microbiome analysis and organic acid level measurements were performed to evaluate the effects of UA intake on the intestinal environment. This clinical trial is publicly registered at the UMIN-CTR, trial number: UMIN000042014. RESULTS: The gut microbiota of the UA 50 mg/day group showed a significant increase in alpha diversity (Faith’s phylogenetic diversity). Four and nine microbial genera were significantly altered in the UA 10 mg/day and UA 50 mg/day groups, respectively (p < 0.05, not corrected). Participants whose FMD scores improved with UA intake had poor baseline FMD values as well as a low Bacillota/Bacteroidota ratio. CONCLUSION: Urolithin A intake alters the gut microbiota and improves their alpha diversity. In addition, the effect of UA on VEF correlated with the individual gut microbiota. Our results have practical implications for a new approach to providing healthcare that focuses on intestinal environment-based diet therapy. Frontiers Media S.A. 2023-01-05 /pmc/articles/PMC9854132/ /pubmed/36687672 http://dx.doi.org/10.3389/fnut.2022.1077534 Text en Copyright © 2023 Nishimoto, Fujisawa, Ukawa, Kudoh, Funahashi, Kishimoto and Fukuda. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Nutrition
Nishimoto, Yuichiro
Fujisawa, Kota
Ukawa, Yuichi
Kudoh, Masatake
Funahashi, Kazuki
Kishimoto, Yoshimi
Fukuda, Shinji
Effect of urolithin A on the improvement of vascular endothelial function depends on the gut microbiota
title Effect of urolithin A on the improvement of vascular endothelial function depends on the gut microbiota
title_full Effect of urolithin A on the improvement of vascular endothelial function depends on the gut microbiota
title_fullStr Effect of urolithin A on the improvement of vascular endothelial function depends on the gut microbiota
title_full_unstemmed Effect of urolithin A on the improvement of vascular endothelial function depends on the gut microbiota
title_short Effect of urolithin A on the improvement of vascular endothelial function depends on the gut microbiota
title_sort effect of urolithin a on the improvement of vascular endothelial function depends on the gut microbiota
topic Nutrition
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9854132/
https://www.ncbi.nlm.nih.gov/pubmed/36687672
http://dx.doi.org/10.3389/fnut.2022.1077534
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