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Alterations in gastric and gut microbiota following sleeve gastrectomy in high-fat diet-induced obese rats
Obesity is considered a high-risk disease and a global epidemic, and the number of obese patients is rising at an alarming rate worldwide. High-fat diet-induced dysbiosis of the intestinal microbiota is considered an essential factor related to obesity. Bariatric surgery induces a sharp decrease in...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10693561/ https://www.ncbi.nlm.nih.gov/pubmed/38042896 http://dx.doi.org/10.1038/s41598-023-48718-w |
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author | Park, Young Suk Ahn, Kung Yun, Kyeongeui Jeong, Jinuk Baek, Kyung-Wan Lee, Jieun Kim, Hyung-Ho Han, Kyudong Ahn, Yong Ju |
author_facet | Park, Young Suk Ahn, Kung Yun, Kyeongeui Jeong, Jinuk Baek, Kyung-Wan Lee, Jieun Kim, Hyung-Ho Han, Kyudong Ahn, Yong Ju |
author_sort | Park, Young Suk |
collection | PubMed |
description | Obesity is considered a high-risk disease and a global epidemic, and the number of obese patients is rising at an alarming rate worldwide. High-fat diet-induced dysbiosis of the intestinal microbiota is considered an essential factor related to obesity. Bariatric surgery induces a sharp decrease in fat content and effectively improves the metabolism of obese individuals. Herein, we aimed to investigate the effects of a high-fat diet-induced obesity and the alterations in gastric and intestinal microbiota resulting from sleeve gastrectomy on clinical outcomes. We performed 16S sequencing of gastric and fecal samples obtained from rats in three treatment groups: normal chow diet, high-fat diet (HFD), and sleeve gastrectomy after HDF for 14 weeks. The area under the curve of fasting glucose and the levels of leptin and low-density lipoproteins were significantly different between groups. Microbial taxa that were highly correlated with several clinical parameters were identified for each group. Glyoxylate and dicarboxylate, taurine and hypotaurine, butanoate, nitrogen, and pyrimidine metabolism and aminoacyl-transfer ribonucleic acid biosynthesis were affected by bariatric surgery and were significantly associated with changes in the composition of gastric and fecal microbiomes. Connectivity and co-occurrence were higher in fecal samples than in gastric tissues. Our results elucidated the positive effects of sleeve gastrectomy in obesity and shed light on changes in the microbiomes of gastric and fecal samples. |
format | Online Article Text |
id | pubmed-10693561 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-106935612023-12-04 Alterations in gastric and gut microbiota following sleeve gastrectomy in high-fat diet-induced obese rats Park, Young Suk Ahn, Kung Yun, Kyeongeui Jeong, Jinuk Baek, Kyung-Wan Lee, Jieun Kim, Hyung-Ho Han, Kyudong Ahn, Yong Ju Sci Rep Article Obesity is considered a high-risk disease and a global epidemic, and the number of obese patients is rising at an alarming rate worldwide. High-fat diet-induced dysbiosis of the intestinal microbiota is considered an essential factor related to obesity. Bariatric surgery induces a sharp decrease in fat content and effectively improves the metabolism of obese individuals. Herein, we aimed to investigate the effects of a high-fat diet-induced obesity and the alterations in gastric and intestinal microbiota resulting from sleeve gastrectomy on clinical outcomes. We performed 16S sequencing of gastric and fecal samples obtained from rats in three treatment groups: normal chow diet, high-fat diet (HFD), and sleeve gastrectomy after HDF for 14 weeks. The area under the curve of fasting glucose and the levels of leptin and low-density lipoproteins were significantly different between groups. Microbial taxa that were highly correlated with several clinical parameters were identified for each group. Glyoxylate and dicarboxylate, taurine and hypotaurine, butanoate, nitrogen, and pyrimidine metabolism and aminoacyl-transfer ribonucleic acid biosynthesis were affected by bariatric surgery and were significantly associated with changes in the composition of gastric and fecal microbiomes. Connectivity and co-occurrence were higher in fecal samples than in gastric tissues. Our results elucidated the positive effects of sleeve gastrectomy in obesity and shed light on changes in the microbiomes of gastric and fecal samples. Nature Publishing Group UK 2023-12-02 /pmc/articles/PMC10693561/ /pubmed/38042896 http://dx.doi.org/10.1038/s41598-023-48718-w Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Park, Young Suk Ahn, Kung Yun, Kyeongeui Jeong, Jinuk Baek, Kyung-Wan Lee, Jieun Kim, Hyung-Ho Han, Kyudong Ahn, Yong Ju Alterations in gastric and gut microbiota following sleeve gastrectomy in high-fat diet-induced obese rats |
title | Alterations in gastric and gut microbiota following sleeve gastrectomy in high-fat diet-induced obese rats |
title_full | Alterations in gastric and gut microbiota following sleeve gastrectomy in high-fat diet-induced obese rats |
title_fullStr | Alterations in gastric and gut microbiota following sleeve gastrectomy in high-fat diet-induced obese rats |
title_full_unstemmed | Alterations in gastric and gut microbiota following sleeve gastrectomy in high-fat diet-induced obese rats |
title_short | Alterations in gastric and gut microbiota following sleeve gastrectomy in high-fat diet-induced obese rats |
title_sort | alterations in gastric and gut microbiota following sleeve gastrectomy in high-fat diet-induced obese rats |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10693561/ https://www.ncbi.nlm.nih.gov/pubmed/38042896 http://dx.doi.org/10.1038/s41598-023-48718-w |
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