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Recent Trends of Microbiota-Based Microbial Metabolites Metabolism in Liver Disease
The gut microbiome and microbial metabolomic influences on liver diseases and their diagnosis, prognosis, and treatment are still controversial. Research studies have provocatively claimed that the gut microbiome, metabolomics understanding, and microbial metabolite screening are key approaches to u...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9125096/ https://www.ncbi.nlm.nih.gov/pubmed/35615096 http://dx.doi.org/10.3389/fmed.2022.841281 |
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author | Ganesan, Raja Jeong, Jin-Ju Kim, Dong Joon Suk, Ki Tae |
author_facet | Ganesan, Raja Jeong, Jin-Ju Kim, Dong Joon Suk, Ki Tae |
author_sort | Ganesan, Raja |
collection | PubMed |
description | The gut microbiome and microbial metabolomic influences on liver diseases and their diagnosis, prognosis, and treatment are still controversial. Research studies have provocatively claimed that the gut microbiome, metabolomics understanding, and microbial metabolite screening are key approaches to understanding liver cancer and liver diseases. An advance of logical innovations in metabolomics profiling, the metabolome inclusion, challenges, and the reproducibility of the investigations at every stage are devoted to this domain to link the common molecules across multiple liver diseases, such as fatty liver, hepatitis, and cirrhosis. These molecules are not immediately recognizable because of the huge underlying and synthetic variety present inside the liver cellular metabolome. This review focuses on microenvironmental metabolic stimuli in the gut-liver axis. Microbial small-molecule profiling (i.e., semiquantitative monitoring, metabolic discrimination, target profiling, and untargeted profiling) in biological fluids has been incompletely addressed. Here, we have reviewed the differential expression of the metabolome of short-chain fatty acids (SCFAs), tryptophan, one-carbon metabolism and bile acid, and the gut microbiota effects are summarized and discussed. We further present proof-of-evidence for gut microbiota-based metabolomics that manipulates the host's gut or liver microbes, mechanosensitive metabolite reactions and potential metabolic pathways. We conclude with a forward-looking perspective on future attention to the “dark matter” of the gut microbiota and microbial metabolomics. |
format | Online Article Text |
id | pubmed-9125096 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-91250962022-05-24 Recent Trends of Microbiota-Based Microbial Metabolites Metabolism in Liver Disease Ganesan, Raja Jeong, Jin-Ju Kim, Dong Joon Suk, Ki Tae Front Med (Lausanne) Medicine The gut microbiome and microbial metabolomic influences on liver diseases and their diagnosis, prognosis, and treatment are still controversial. Research studies have provocatively claimed that the gut microbiome, metabolomics understanding, and microbial metabolite screening are key approaches to understanding liver cancer and liver diseases. An advance of logical innovations in metabolomics profiling, the metabolome inclusion, challenges, and the reproducibility of the investigations at every stage are devoted to this domain to link the common molecules across multiple liver diseases, such as fatty liver, hepatitis, and cirrhosis. These molecules are not immediately recognizable because of the huge underlying and synthetic variety present inside the liver cellular metabolome. This review focuses on microenvironmental metabolic stimuli in the gut-liver axis. Microbial small-molecule profiling (i.e., semiquantitative monitoring, metabolic discrimination, target profiling, and untargeted profiling) in biological fluids has been incompletely addressed. Here, we have reviewed the differential expression of the metabolome of short-chain fatty acids (SCFAs), tryptophan, one-carbon metabolism and bile acid, and the gut microbiota effects are summarized and discussed. We further present proof-of-evidence for gut microbiota-based metabolomics that manipulates the host's gut or liver microbes, mechanosensitive metabolite reactions and potential metabolic pathways. We conclude with a forward-looking perspective on future attention to the “dark matter” of the gut microbiota and microbial metabolomics. Frontiers Media S.A. 2022-05-09 /pmc/articles/PMC9125096/ /pubmed/35615096 http://dx.doi.org/10.3389/fmed.2022.841281 Text en Copyright © 2022 Ganesan, Jeong, Kim and Suk. 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 | Medicine Ganesan, Raja Jeong, Jin-Ju Kim, Dong Joon Suk, Ki Tae Recent Trends of Microbiota-Based Microbial Metabolites Metabolism in Liver Disease |
title | Recent Trends of Microbiota-Based Microbial Metabolites Metabolism in Liver Disease |
title_full | Recent Trends of Microbiota-Based Microbial Metabolites Metabolism in Liver Disease |
title_fullStr | Recent Trends of Microbiota-Based Microbial Metabolites Metabolism in Liver Disease |
title_full_unstemmed | Recent Trends of Microbiota-Based Microbial Metabolites Metabolism in Liver Disease |
title_short | Recent Trends of Microbiota-Based Microbial Metabolites Metabolism in Liver Disease |
title_sort | recent trends of microbiota-based microbial metabolites metabolism in liver disease |
topic | Medicine |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9125096/ https://www.ncbi.nlm.nih.gov/pubmed/35615096 http://dx.doi.org/10.3389/fmed.2022.841281 |
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