Accumulating evidence supports a relationship between the complexity and diversity of the gut microbiota and host diseases. In addition to alterations in the gut microbial composition, the metabolic potential of gut microbiota has been identified as a contributing factor in the development of diseases. Recent technological developments of molecular and biochemical analyses enable us to detect and characterize the gut microbiota via assessment and classification of its genomes and corresponding metabolites. These advances have provided emerging data supporting the role of gut microbiota in various physiological activities including host metabolism, neurological development, energy homeostasis, and immune regulation. Although few human studies have looked into the causative associations and underlying pathophysiology of the gut microbiota and host disease, a growing body of preclinical and clinical evidence supports the theory that the gut microbiota and its metabolites have the potential to be a novel therapeutic and preventative target for cardiovascular and metabolic diseases. In this review, we highlight the interplay between the gut microbiota and its metabolites, and the development and progression of hypertension, heart failure, and chronic kidney disease.
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January 2018
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Oleic-acid-treated HepG2 cells immunostained for PGC-1α (PPARγ co-activator-1 α). In Clinical Science volume 132, issue 1, the results of work by Bernardi et al. include reporting that the protein TRAIL (TNF-related apoptosis inducing ligand) increases the expression of PGC-1α in HepG2 cells cultured with oleic acid. Overall, the article points to a potential therapeutic role for TRAIL against impaired glucose tolerance and non-alcoholic fatty liver disease; for details see pages 69–83.
Review Article|
January 11 2018
Gut microbiota in cardiovascular disease and heart failure
Takeshi Kitai;
Takeshi Kitai
1Department of Cardiovascular Medicine, Heart and Vascular Institute, Cleveland Clinic, Cleveland, OH, U.S.A.
2Department of Cardiovascular Medicine, Kobe City Medical Center General Hospital, Kobe, Japan
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W.H. Wilson Tang
1Department of Cardiovascular Medicine, Heart and Vascular Institute, Cleveland Clinic, Cleveland, OH, U.S.A.
3Center for Clinical Genomics, Cleveland Clinic, Cleveland, OH, U.S.A.
Correspondence: W.H. Wilson Tang ([email protected])
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Publisher: Portland Press Ltd
Received:
September 02 2017
Revision Received:
November 15 2017
Accepted:
November 20 2017
Online ISSN: 1470-8736
Print ISSN: 0143-5221
© 2018 The Author(s). Published by Portland Press Limited on behalf of the Biochemical Society
2018
Clin Sci (Lond) (2018) 132 (1): 85–91.
Article history
Received:
September 02 2017
Revision Received:
November 15 2017
Accepted:
November 20 2017
Citation
Takeshi Kitai, W.H. Wilson Tang; Gut microbiota in cardiovascular disease and heart failure. Clin Sci (Lond) 16 January 2018; 132 (1): 85–91. doi: https://doi.org/10.1042/CS20171090
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