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Grape polyphenols reduce gut-localized reactive oxygen species associated with the development of metabolic syndrome in mice

High-fat diet (HFD)-induced leaky gut syndrome combined with low-grade inflammation increase reactive oxygen species (ROS) in the intestine and may contribute to dysbiosis and metabolic syndrome (MetS). Poorly bioavailable and only partially metabolizable dietary polyphenols, such as proanthocyanidi...

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Autores principales: Kuhn, Peter, Kalariya, Hetalben M., Poulev, Alexander, Ribnicky, David M., Jaja-Chimedza, Asha, Roopchand, Diana E., Raskin, Ilya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6181265/
https://www.ncbi.nlm.nih.gov/pubmed/30308002
http://dx.doi.org/10.1371/journal.pone.0198716
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author Kuhn, Peter
Kalariya, Hetalben M.
Poulev, Alexander
Ribnicky, David M.
Jaja-Chimedza, Asha
Roopchand, Diana E.
Raskin, Ilya
author_facet Kuhn, Peter
Kalariya, Hetalben M.
Poulev, Alexander
Ribnicky, David M.
Jaja-Chimedza, Asha
Roopchand, Diana E.
Raskin, Ilya
author_sort Kuhn, Peter
collection PubMed
description High-fat diet (HFD)-induced leaky gut syndrome combined with low-grade inflammation increase reactive oxygen species (ROS) in the intestine and may contribute to dysbiosis and metabolic syndrome (MetS). Poorly bioavailable and only partially metabolizable dietary polyphenols, such as proanthocyanidins (PACs), may exert their beneficial effects on metabolic health by scavenging intestinal ROS. To test this hypothesis, we developed and validated a novel, noninvasive, in situ method for visualizing intestinal ROS using orally administered ROS-sensitive indocyanine green (ICG) dye. C57BL/6J mice fed HFD for 10 weeks accumulated high levels of intestinal ROS compared to mice fed low-fat diet (LFD). Oral administration of poorly bioavailable grape polyphenol extract (GPE) and β-carotene decreased HFD-induced ROS in the gut to levels comparable to LFD-fed mice, while administration of more bioavailable dietary antioxidants (α-lipoic acid, vitamin C, vitamin E) did not. Forty percent of administered GPE antioxidant activity was measured in feces collected over 24 h, confirming poor bioavailability and persistence in the gut. The bloom of beneficial anaerobic gut bacteria, such as Akkermansia muciniphila, associated with improved metabolic status in rodents and humans may be directly linked to protective antioxidant activity of some dietary components. These findings suggest a possible mechanistic explanation for the beneficial effects of poorly bioavailable polyphenols on metabolic health.
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spelling pubmed-61812652018-10-26 Grape polyphenols reduce gut-localized reactive oxygen species associated with the development of metabolic syndrome in mice Kuhn, Peter Kalariya, Hetalben M. Poulev, Alexander Ribnicky, David M. Jaja-Chimedza, Asha Roopchand, Diana E. Raskin, Ilya PLoS One Research Article High-fat diet (HFD)-induced leaky gut syndrome combined with low-grade inflammation increase reactive oxygen species (ROS) in the intestine and may contribute to dysbiosis and metabolic syndrome (MetS). Poorly bioavailable and only partially metabolizable dietary polyphenols, such as proanthocyanidins (PACs), may exert their beneficial effects on metabolic health by scavenging intestinal ROS. To test this hypothesis, we developed and validated a novel, noninvasive, in situ method for visualizing intestinal ROS using orally administered ROS-sensitive indocyanine green (ICG) dye. C57BL/6J mice fed HFD for 10 weeks accumulated high levels of intestinal ROS compared to mice fed low-fat diet (LFD). Oral administration of poorly bioavailable grape polyphenol extract (GPE) and β-carotene decreased HFD-induced ROS in the gut to levels comparable to LFD-fed mice, while administration of more bioavailable dietary antioxidants (α-lipoic acid, vitamin C, vitamin E) did not. Forty percent of administered GPE antioxidant activity was measured in feces collected over 24 h, confirming poor bioavailability and persistence in the gut. The bloom of beneficial anaerobic gut bacteria, such as Akkermansia muciniphila, associated with improved metabolic status in rodents and humans may be directly linked to protective antioxidant activity of some dietary components. These findings suggest a possible mechanistic explanation for the beneficial effects of poorly bioavailable polyphenols on metabolic health. Public Library of Science 2018-10-11 /pmc/articles/PMC6181265/ /pubmed/30308002 http://dx.doi.org/10.1371/journal.pone.0198716 Text en © 2018 Kuhn et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Kuhn, Peter
Kalariya, Hetalben M.
Poulev, Alexander
Ribnicky, David M.
Jaja-Chimedza, Asha
Roopchand, Diana E.
Raskin, Ilya
Grape polyphenols reduce gut-localized reactive oxygen species associated with the development of metabolic syndrome in mice
title Grape polyphenols reduce gut-localized reactive oxygen species associated with the development of metabolic syndrome in mice
title_full Grape polyphenols reduce gut-localized reactive oxygen species associated with the development of metabolic syndrome in mice
title_fullStr Grape polyphenols reduce gut-localized reactive oxygen species associated with the development of metabolic syndrome in mice
title_full_unstemmed Grape polyphenols reduce gut-localized reactive oxygen species associated with the development of metabolic syndrome in mice
title_short Grape polyphenols reduce gut-localized reactive oxygen species associated with the development of metabolic syndrome in mice
title_sort grape polyphenols reduce gut-localized reactive oxygen species associated with the development of metabolic syndrome in mice
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6181265/
https://www.ncbi.nlm.nih.gov/pubmed/30308002
http://dx.doi.org/10.1371/journal.pone.0198716
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