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Gut-Microbiota Dysbiosis in Stroke-Prone Spontaneously Hypertensive Rats with Diet-Induced Steatohepatitis

Metabolic-dysfunction-associated fatty-liver disease (MAFLD) is the principal worldwide cause of liver disease. Individuals with nonalcoholic steatohepatitis (NASH) have a higher prevalence of small-intestinal bacterial overgrowth (SIBO). We examined gut-microbiota isolated from 12-week-old stroke-p...

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Autores principales: Kanezawa, Shini, Moriyama, Mitsuhiko, Kanda, Tatsuo, Fukushima, Akiko, Masuzaki, Ryota, Sasaki-Tanaka, Reina, Tsunemi, Akiko, Ueno, Takahiro, Fukuda, Noboru, Kogure, Hirofumi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10002594/
https://www.ncbi.nlm.nih.gov/pubmed/36902037
http://dx.doi.org/10.3390/ijms24054603
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author Kanezawa, Shini
Moriyama, Mitsuhiko
Kanda, Tatsuo
Fukushima, Akiko
Masuzaki, Ryota
Sasaki-Tanaka, Reina
Tsunemi, Akiko
Ueno, Takahiro
Fukuda, Noboru
Kogure, Hirofumi
author_facet Kanezawa, Shini
Moriyama, Mitsuhiko
Kanda, Tatsuo
Fukushima, Akiko
Masuzaki, Ryota
Sasaki-Tanaka, Reina
Tsunemi, Akiko
Ueno, Takahiro
Fukuda, Noboru
Kogure, Hirofumi
author_sort Kanezawa, Shini
collection PubMed
description Metabolic-dysfunction-associated fatty-liver disease (MAFLD) is the principal worldwide cause of liver disease. Individuals with nonalcoholic steatohepatitis (NASH) have a higher prevalence of small-intestinal bacterial overgrowth (SIBO). We examined gut-microbiota isolated from 12-week-old stroke-prone spontaneously hypertensive-5 rats (SHRSP5) fed on a normal diet (ND) or a high-fat- and high-cholesterol-containing diet (HFCD) and clarified the differences between their gut-microbiota. We observed that the Firmicute/Bacteroidetes (F/B) ratio in both the small intestines and the feces of the SHRSP5 rats fed HFCD increased compared to that of the SHRSP5 rats fed ND. Notably, the quantities of the 16S rRNA genes in small intestines of the SHRSP5 rats fed HFCD were significantly lower than those of the SHRSP5 rats fed ND. As in SIBO syndrome, the SHRSP5 rats fed HFCD presented with diarrhea and body-weight loss with abnormal types of bacteria in the small intestine, although the number of bacteria in the small intestine did not increase. The microbiota of the feces in the SHRSP5 rats fed HFCD was different from those in the SHRP5 rats fed ND. In conclusion, there is an association between MAFLD and gut-microbiota alteration. Gut-microbiota alteration may be a therapeutic target for MAFLD.
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spelling pubmed-100025942023-03-11 Gut-Microbiota Dysbiosis in Stroke-Prone Spontaneously Hypertensive Rats with Diet-Induced Steatohepatitis Kanezawa, Shini Moriyama, Mitsuhiko Kanda, Tatsuo Fukushima, Akiko Masuzaki, Ryota Sasaki-Tanaka, Reina Tsunemi, Akiko Ueno, Takahiro Fukuda, Noboru Kogure, Hirofumi Int J Mol Sci Article Metabolic-dysfunction-associated fatty-liver disease (MAFLD) is the principal worldwide cause of liver disease. Individuals with nonalcoholic steatohepatitis (NASH) have a higher prevalence of small-intestinal bacterial overgrowth (SIBO). We examined gut-microbiota isolated from 12-week-old stroke-prone spontaneously hypertensive-5 rats (SHRSP5) fed on a normal diet (ND) or a high-fat- and high-cholesterol-containing diet (HFCD) and clarified the differences between their gut-microbiota. We observed that the Firmicute/Bacteroidetes (F/B) ratio in both the small intestines and the feces of the SHRSP5 rats fed HFCD increased compared to that of the SHRSP5 rats fed ND. Notably, the quantities of the 16S rRNA genes in small intestines of the SHRSP5 rats fed HFCD were significantly lower than those of the SHRSP5 rats fed ND. As in SIBO syndrome, the SHRSP5 rats fed HFCD presented with diarrhea and body-weight loss with abnormal types of bacteria in the small intestine, although the number of bacteria in the small intestine did not increase. The microbiota of the feces in the SHRSP5 rats fed HFCD was different from those in the SHRP5 rats fed ND. In conclusion, there is an association between MAFLD and gut-microbiota alteration. Gut-microbiota alteration may be a therapeutic target for MAFLD. MDPI 2023-02-27 /pmc/articles/PMC10002594/ /pubmed/36902037 http://dx.doi.org/10.3390/ijms24054603 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Kanezawa, Shini
Moriyama, Mitsuhiko
Kanda, Tatsuo
Fukushima, Akiko
Masuzaki, Ryota
Sasaki-Tanaka, Reina
Tsunemi, Akiko
Ueno, Takahiro
Fukuda, Noboru
Kogure, Hirofumi
Gut-Microbiota Dysbiosis in Stroke-Prone Spontaneously Hypertensive Rats with Diet-Induced Steatohepatitis
title Gut-Microbiota Dysbiosis in Stroke-Prone Spontaneously Hypertensive Rats with Diet-Induced Steatohepatitis
title_full Gut-Microbiota Dysbiosis in Stroke-Prone Spontaneously Hypertensive Rats with Diet-Induced Steatohepatitis
title_fullStr Gut-Microbiota Dysbiosis in Stroke-Prone Spontaneously Hypertensive Rats with Diet-Induced Steatohepatitis
title_full_unstemmed Gut-Microbiota Dysbiosis in Stroke-Prone Spontaneously Hypertensive Rats with Diet-Induced Steatohepatitis
title_short Gut-Microbiota Dysbiosis in Stroke-Prone Spontaneously Hypertensive Rats with Diet-Induced Steatohepatitis
title_sort gut-microbiota dysbiosis in stroke-prone spontaneously hypertensive rats with diet-induced steatohepatitis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10002594/
https://www.ncbi.nlm.nih.gov/pubmed/36902037
http://dx.doi.org/10.3390/ijms24054603
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