Cross-Talk between Gut Microbiota and Heart via the Routes of Metabolite and Immunity

Considering the prevalence of cardiovascular disease (CVD), significant interest has been focused on the gut microbiota-heart interaction because the gut microbiota has been recognized as a barometer of human health. Dysbiosis, characterized by changes in the gut microbiota in CVD, has been reported...

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Main Authors: Jin Bu, Zhaohui Wang
Format: Article
Language:English
Published: Hindawi Limited 2018-01-01
Series:Gastroenterology Research and Practice
Online Access:http://dx.doi.org/10.1155/2018/6458094
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spelling doaj-ce1d84cf27434e0da12d4a8660f38dfd2020-11-24T20:58:08ZengHindawi LimitedGastroenterology Research and Practice1687-61211687-630X2018-01-01201810.1155/2018/64580946458094Cross-Talk between Gut Microbiota and Heart via the Routes of Metabolite and ImmunityJin Bu0Zhaohui Wang1Department of Geriatrics, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430022, ChinaDepartment of Geriatrics, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430022, ChinaConsidering the prevalence of cardiovascular disease (CVD), significant interest has been focused on the gut microbiota-heart interaction because the gut microbiota has been recognized as a barometer of human health. Dysbiosis, characterized by changes in the gut microbiota in CVD, has been reported in cardiovascular pathologies, such as atherosclerosis, hypertension, and heart failure. Conversely, gut microbiota-derived metabolites, such as trimethylamine/trimethylamine N-oxide (TMA/TMAO), can impact host physiology. Further, bacterial dysbiosis can disturb gut immunity, which increases the risk of acute arterial events. Moreover, studies of germ-free mice have provided evidence that microbiota diversity and the presence of a specific microbe in the gut can affect immune cells in hosts. Therefore, the changes in the composition of the gut microbiota can affect host metabolism and immunity. Importantly, these effects are not only confined to the gut but also spreaded to distal organs. The purpose of the current review is to highlight the complex interplay between the microbiota and CVD via TMAO and different immune cells and discuss the roles of probiotics and nutrition interventions in modulating the intestinal microbiota as novel therapeutic targets of CVD.http://dx.doi.org/10.1155/2018/6458094
collection DOAJ
language English
format Article
sources DOAJ
author Jin Bu
Zhaohui Wang
spellingShingle Jin Bu
Zhaohui Wang
Cross-Talk between Gut Microbiota and Heart via the Routes of Metabolite and Immunity
Gastroenterology Research and Practice
author_facet Jin Bu
Zhaohui Wang
author_sort Jin Bu
title Cross-Talk between Gut Microbiota and Heart via the Routes of Metabolite and Immunity
title_short Cross-Talk between Gut Microbiota and Heart via the Routes of Metabolite and Immunity
title_full Cross-Talk between Gut Microbiota and Heart via the Routes of Metabolite and Immunity
title_fullStr Cross-Talk between Gut Microbiota and Heart via the Routes of Metabolite and Immunity
title_full_unstemmed Cross-Talk between Gut Microbiota and Heart via the Routes of Metabolite and Immunity
title_sort cross-talk between gut microbiota and heart via the routes of metabolite and immunity
publisher Hindawi Limited
series Gastroenterology Research and Practice
issn 1687-6121
1687-630X
publishDate 2018-01-01
description Considering the prevalence of cardiovascular disease (CVD), significant interest has been focused on the gut microbiota-heart interaction because the gut microbiota has been recognized as a barometer of human health. Dysbiosis, characterized by changes in the gut microbiota in CVD, has been reported in cardiovascular pathologies, such as atherosclerosis, hypertension, and heart failure. Conversely, gut microbiota-derived metabolites, such as trimethylamine/trimethylamine N-oxide (TMA/TMAO), can impact host physiology. Further, bacterial dysbiosis can disturb gut immunity, which increases the risk of acute arterial events. Moreover, studies of germ-free mice have provided evidence that microbiota diversity and the presence of a specific microbe in the gut can affect immune cells in hosts. Therefore, the changes in the composition of the gut microbiota can affect host metabolism and immunity. Importantly, these effects are not only confined to the gut but also spreaded to distal organs. The purpose of the current review is to highlight the complex interplay between the microbiota and CVD via TMAO and different immune cells and discuss the roles of probiotics and nutrition interventions in modulating the intestinal microbiota as novel therapeutic targets of CVD.
url http://dx.doi.org/10.1155/2018/6458094
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