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New insights into the links between anti-diabetes drugs and gut microbiota

In patients with type 2 diabetes mellitus (T2DM), the intestinal flora is out of balance and accompanied by leaky gut. The flora is characterized by an increase in mucus-degrading bacteria and a decrease in fiber-degrading bacteria. Short-chain fatty acids (SCFAs), as the major fiber-degrading bacte...

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Autores principales: Hu, Ruixin, Yuan, Yanting, Liu, Chaolong, Zhou, Ji, Ji, Lixia, Jiang, Guohui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bioscientifica Ltd 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7923145/
https://www.ncbi.nlm.nih.gov/pubmed/33338029
http://dx.doi.org/10.1530/EC-20-0431
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author Hu, Ruixin
Yuan, Yanting
Liu, Chaolong
Zhou, Ji
Ji, Lixia
Jiang, Guohui
author_facet Hu, Ruixin
Yuan, Yanting
Liu, Chaolong
Zhou, Ji
Ji, Lixia
Jiang, Guohui
author_sort Hu, Ruixin
collection PubMed
description In patients with type 2 diabetes mellitus (T2DM), the intestinal flora is out of balance and accompanied by leaky gut. The flora is characterized by an increase in mucus-degrading bacteria and a decrease in fiber-degrading bacteria. Short-chain fatty acids (SCFAs), as the major fiber-degrading bacteria fermentation, not only ameliorate the leaky gut, but also activate GPR43 to increase the mass of functional pancreatic β-cells and exert anti-inflammation effect. At present, the gut microbiota is considered as the potential target for anti-diabetes drugs, and how to reverse the imbalance of gut microbiota has become a therapeutic strategy for T2DM. This review briefly summarizes the drugs or compounds that have direct or potential therapeutic effects on T2DM by modulating the gut microbiota, including biguanides, isoquinoline alkaloids, stilbene and C7N-aminocyclic alcohols.
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spelling pubmed-79231452021-03-05 New insights into the links between anti-diabetes drugs and gut microbiota Hu, Ruixin Yuan, Yanting Liu, Chaolong Zhou, Ji Ji, Lixia Jiang, Guohui Endocr Connect Review In patients with type 2 diabetes mellitus (T2DM), the intestinal flora is out of balance and accompanied by leaky gut. The flora is characterized by an increase in mucus-degrading bacteria and a decrease in fiber-degrading bacteria. Short-chain fatty acids (SCFAs), as the major fiber-degrading bacteria fermentation, not only ameliorate the leaky gut, but also activate GPR43 to increase the mass of functional pancreatic β-cells and exert anti-inflammation effect. At present, the gut microbiota is considered as the potential target for anti-diabetes drugs, and how to reverse the imbalance of gut microbiota has become a therapeutic strategy for T2DM. This review briefly summarizes the drugs or compounds that have direct or potential therapeutic effects on T2DM by modulating the gut microbiota, including biguanides, isoquinoline alkaloids, stilbene and C7N-aminocyclic alcohols. Bioscientifica Ltd 2020-12-17 /pmc/articles/PMC7923145/ /pubmed/33338029 http://dx.doi.org/10.1530/EC-20-0431 Text en © 2021 The authors http://creativecommons.org/licenses/by-nc/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License. (http://creativecommons.org/licenses/by-nc/4.0/)
spellingShingle Review
Hu, Ruixin
Yuan, Yanting
Liu, Chaolong
Zhou, Ji
Ji, Lixia
Jiang, Guohui
New insights into the links between anti-diabetes drugs and gut microbiota
title New insights into the links between anti-diabetes drugs and gut microbiota
title_full New insights into the links between anti-diabetes drugs and gut microbiota
title_fullStr New insights into the links between anti-diabetes drugs and gut microbiota
title_full_unstemmed New insights into the links between anti-diabetes drugs and gut microbiota
title_short New insights into the links between anti-diabetes drugs and gut microbiota
title_sort new insights into the links between anti-diabetes drugs and gut microbiota
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7923145/
https://www.ncbi.nlm.nih.gov/pubmed/33338029
http://dx.doi.org/10.1530/EC-20-0431
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