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Anti-aging effects of a functional food via the action of gut microbiota and metabolites in aging mice

Wushen (WS) is a mixed food containing 55 natural products that is beneficial to human health. This study aimed to reveal the preventive effect of WS on aging via a combined analysis of gut microbiome and metabolome. Senescence-accelerated mouse prone 8 (SAMP8) mice were used as aging model and sene...

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Autores principales: Zhang, Jie, Chen, Zhewen, Yu, Huaixi, Lu, Yanwen, Yu, Weinan, Miao, Mingyong, Shi, Hanping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8312451/
https://www.ncbi.nlm.nih.gov/pubmed/33878733
http://dx.doi.org/10.18632/aging.202873
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author Zhang, Jie
Chen, Zhewen
Yu, Huaixi
Lu, Yanwen
Yu, Weinan
Miao, Mingyong
Shi, Hanping
author_facet Zhang, Jie
Chen, Zhewen
Yu, Huaixi
Lu, Yanwen
Yu, Weinan
Miao, Mingyong
Shi, Hanping
author_sort Zhang, Jie
collection PubMed
description Wushen (WS) is a mixed food containing 55 natural products that is beneficial to human health. This study aimed to reveal the preventive effect of WS on aging via a combined analysis of gut microbiome and metabolome. Senescence-accelerated mouse prone 8 (SAMP8) mice were used as aging model and senescence-accelerated mouse resistant 1 (SAMR1) mice as control. The mice were fed four diet types; control diet (for SAMR1 mice), standard diet (for SAMP8 mice, as SD group), WS diet, and fecal microbiota transplantation (FMT; transplanted from aging-WS mice). Our results showed that the weight, food intake, neurological function, and general physical conditions significantly improved in WS-fed mice compared to those fed with SD. The CA1 hippocampal region in WS-fed aged mice showed fewer shriveled neurons and increased neuronal layers compared to that of the SD group. WS-fed mice showed a decrease in malondialdehyde and an increase in superoxide dismutase levels in the brain; additionally, IL-6 and TNF-α levels significantly decreased, whereas IL-2 levels and the proportion of lymphocytes, CD3+CD8+ T, and CD4+IFNγ+T cells increased in WS-fed mice. After fed with WS, the abundance of Ruminococcus and Butyrivibrio markedly increased, whereas Lachnoclostridium and Ruminiclostridium significantly decreased in the aging mice. In addition, 887 differentially expressed metabolites were identified in fecal samples, among these, Butyrivibrio was positively correlated with D-glucuronic acid and Ruminococcus was positively associated with 5-acetamidovalerate. These findings provide mechanistic insight into the impact of WS on aging, and WS may be a valuable diet for preventing aging.
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spelling pubmed-83124512021-07-27 Anti-aging effects of a functional food via the action of gut microbiota and metabolites in aging mice Zhang, Jie Chen, Zhewen Yu, Huaixi Lu, Yanwen Yu, Weinan Miao, Mingyong Shi, Hanping Aging (Albany NY) Research Paper Wushen (WS) is a mixed food containing 55 natural products that is beneficial to human health. This study aimed to reveal the preventive effect of WS on aging via a combined analysis of gut microbiome and metabolome. Senescence-accelerated mouse prone 8 (SAMP8) mice were used as aging model and senescence-accelerated mouse resistant 1 (SAMR1) mice as control. The mice were fed four diet types; control diet (for SAMR1 mice), standard diet (for SAMP8 mice, as SD group), WS diet, and fecal microbiota transplantation (FMT; transplanted from aging-WS mice). Our results showed that the weight, food intake, neurological function, and general physical conditions significantly improved in WS-fed mice compared to those fed with SD. The CA1 hippocampal region in WS-fed aged mice showed fewer shriveled neurons and increased neuronal layers compared to that of the SD group. WS-fed mice showed a decrease in malondialdehyde and an increase in superoxide dismutase levels in the brain; additionally, IL-6 and TNF-α levels significantly decreased, whereas IL-2 levels and the proportion of lymphocytes, CD3+CD8+ T, and CD4+IFNγ+T cells increased in WS-fed mice. After fed with WS, the abundance of Ruminococcus and Butyrivibrio markedly increased, whereas Lachnoclostridium and Ruminiclostridium significantly decreased in the aging mice. In addition, 887 differentially expressed metabolites were identified in fecal samples, among these, Butyrivibrio was positively correlated with D-glucuronic acid and Ruminococcus was positively associated with 5-acetamidovalerate. These findings provide mechanistic insight into the impact of WS on aging, and WS may be a valuable diet for preventing aging. Impact Journals 2021-04-20 /pmc/articles/PMC8312451/ /pubmed/33878733 http://dx.doi.org/10.18632/aging.202873 Text en Copyright: © 2021 Zhang et al. https://creativecommons.org/licenses/by/3.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/3.0/) (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Zhang, Jie
Chen, Zhewen
Yu, Huaixi
Lu, Yanwen
Yu, Weinan
Miao, Mingyong
Shi, Hanping
Anti-aging effects of a functional food via the action of gut microbiota and metabolites in aging mice
title Anti-aging effects of a functional food via the action of gut microbiota and metabolites in aging mice
title_full Anti-aging effects of a functional food via the action of gut microbiota and metabolites in aging mice
title_fullStr Anti-aging effects of a functional food via the action of gut microbiota and metabolites in aging mice
title_full_unstemmed Anti-aging effects of a functional food via the action of gut microbiota and metabolites in aging mice
title_short Anti-aging effects of a functional food via the action of gut microbiota and metabolites in aging mice
title_sort anti-aging effects of a functional food via the action of gut microbiota and metabolites in aging mice
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8312451/
https://www.ncbi.nlm.nih.gov/pubmed/33878733
http://dx.doi.org/10.18632/aging.202873
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