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The relationship between gut microbiota and susceptibility to type 2 diabetes mellitus in rats

PURPOSE: The purpose of this study is to investigate the relationship between the susceptibility to type 2 diabetes and gut microbiota in rats and to explore the potential mechanism involved. METHODS: Thirty-two SPF-grade SD rats were raised as donor rats, and divided into control, type 2 diabetes m...

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Autores principales: An, Yongcheng, Dai, Hongyu, Duan, Yuhui, Cheng, Long, Shi, Lu, He, Changhao, Wang, Chen, Lv, Yinglan, Li, Huimin, Zhang, Huilin, Huang, Yan, Fu, Wanxin, Sun, Weiguang, Zhao, Baosheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10161507/
https://www.ncbi.nlm.nih.gov/pubmed/37147692
http://dx.doi.org/10.1186/s13020-023-00717-9
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author An, Yongcheng
Dai, Hongyu
Duan, Yuhui
Cheng, Long
Shi, Lu
He, Changhao
Wang, Chen
Lv, Yinglan
Li, Huimin
Zhang, Huilin
Huang, Yan
Fu, Wanxin
Sun, Weiguang
Zhao, Baosheng
author_facet An, Yongcheng
Dai, Hongyu
Duan, Yuhui
Cheng, Long
Shi, Lu
He, Changhao
Wang, Chen
Lv, Yinglan
Li, Huimin
Zhang, Huilin
Huang, Yan
Fu, Wanxin
Sun, Weiguang
Zhao, Baosheng
author_sort An, Yongcheng
collection PubMed
description PURPOSE: The purpose of this study is to investigate the relationship between the susceptibility to type 2 diabetes and gut microbiota in rats and to explore the potential mechanism involved. METHODS: Thirty-two SPF-grade SD rats were raised as donor rats, and divided into control, type 2 diabetes mellitus (T2DM, fasting blood glucose ≥ 11.1 mmol/L), and Non-T2DM (fasting blood glucose < 11.1 mmol/L) groups. Feces were collected and prepared as fecal bacteria supernatants Diab (fecal bacteria supernatant of T2DM group rats), Non (fecal bacteria supernatant of Non-T2DM group rats), and Con (fecal bacteria supernatant of control group rats). Another seventy-nine SPF-grade SD rats were separated into normal saline (NS) and antibiotics (ABX) groups and given normal saline and antibiotics solutions, respectively. In addition, the ABX group rats were randomly separated into ABX-ord (fed with a 4-week ordinary diet), ABX-fat (fed with a 4-week high-fat diet and STZ ip), FMT-Diab (with transplanted fecal bacteria supernatant Diab and fed with a 4-week high-fat diet and STZ ip), FMT-Non (with transplanted fecal bacteria supernatant Non and fed with a 4-week high-fat diet and STZ ip), and FMT-Con (with transplanted fecal bacteria supernatant Con and fed with a 4-week high-fat diet and STZ ip) groups. Furthermore, the NS group was randomly divided into NS-ord (fed with a 4-week ordinary diet) and NS-fat (fed with a 4-week high-fat diet and STZ ip) groups. After this, the short-chain fatty acids (SCFAs) in the feces were detected using gas chromatography, and the gut microbiota were detected using 16S rRNA gene sequencing. Finally, G protein-coupled receptor 41 (GPR41) and GPR43 were detected by western blot and quantitative real-time polymerase chain reaction. RESULTS: G__Ruminococcus_gnavus_group were more abundant in the FMT-Diab group compared to the ABX-fat and FMT-Non groups. The levels of blood glucose, serum insulin, total cholesterol, triglycerides, and low-density lipoprotein cholesterol were also higher in the FMT-Diab group compared to those of the ABX-fat group. Compared to the ABX-fat group, both the FMT-Diab and FMT-Non groups had higher contents of acetic and butyric acid, and the expression of GPR41/43 were significantly higher as well. CONCLUSIONS: G__Ruminococcus_gnavus_group might make rats more susceptible to T2DM; T2DM-susceptible flora transplantation increased the susceptibility to T2DM in rats. Additionally, gut microbiota-SCFAs-GPR41/43 may play a role in the development of T2DM. Lowering blood glucose by regulating gut microbiota may therefore become a new strategy for the treatment of T2DM in humans. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13020-023-00717-9.
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spelling pubmed-101615072023-05-06 The relationship between gut microbiota and susceptibility to type 2 diabetes mellitus in rats An, Yongcheng Dai, Hongyu Duan, Yuhui Cheng, Long Shi, Lu He, Changhao Wang, Chen Lv, Yinglan Li, Huimin Zhang, Huilin Huang, Yan Fu, Wanxin Sun, Weiguang Zhao, Baosheng Chin Med Research PURPOSE: The purpose of this study is to investigate the relationship between the susceptibility to type 2 diabetes and gut microbiota in rats and to explore the potential mechanism involved. METHODS: Thirty-two SPF-grade SD rats were raised as donor rats, and divided into control, type 2 diabetes mellitus (T2DM, fasting blood glucose ≥ 11.1 mmol/L), and Non-T2DM (fasting blood glucose < 11.1 mmol/L) groups. Feces were collected and prepared as fecal bacteria supernatants Diab (fecal bacteria supernatant of T2DM group rats), Non (fecal bacteria supernatant of Non-T2DM group rats), and Con (fecal bacteria supernatant of control group rats). Another seventy-nine SPF-grade SD rats were separated into normal saline (NS) and antibiotics (ABX) groups and given normal saline and antibiotics solutions, respectively. In addition, the ABX group rats were randomly separated into ABX-ord (fed with a 4-week ordinary diet), ABX-fat (fed with a 4-week high-fat diet and STZ ip), FMT-Diab (with transplanted fecal bacteria supernatant Diab and fed with a 4-week high-fat diet and STZ ip), FMT-Non (with transplanted fecal bacteria supernatant Non and fed with a 4-week high-fat diet and STZ ip), and FMT-Con (with transplanted fecal bacteria supernatant Con and fed with a 4-week high-fat diet and STZ ip) groups. Furthermore, the NS group was randomly divided into NS-ord (fed with a 4-week ordinary diet) and NS-fat (fed with a 4-week high-fat diet and STZ ip) groups. After this, the short-chain fatty acids (SCFAs) in the feces were detected using gas chromatography, and the gut microbiota were detected using 16S rRNA gene sequencing. Finally, G protein-coupled receptor 41 (GPR41) and GPR43 were detected by western blot and quantitative real-time polymerase chain reaction. RESULTS: G__Ruminococcus_gnavus_group were more abundant in the FMT-Diab group compared to the ABX-fat and FMT-Non groups. The levels of blood glucose, serum insulin, total cholesterol, triglycerides, and low-density lipoprotein cholesterol were also higher in the FMT-Diab group compared to those of the ABX-fat group. Compared to the ABX-fat group, both the FMT-Diab and FMT-Non groups had higher contents of acetic and butyric acid, and the expression of GPR41/43 were significantly higher as well. CONCLUSIONS: G__Ruminococcus_gnavus_group might make rats more susceptible to T2DM; T2DM-susceptible flora transplantation increased the susceptibility to T2DM in rats. Additionally, gut microbiota-SCFAs-GPR41/43 may play a role in the development of T2DM. Lowering blood glucose by regulating gut microbiota may therefore become a new strategy for the treatment of T2DM in humans. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13020-023-00717-9. BioMed Central 2023-05-05 /pmc/articles/PMC10161507/ /pubmed/37147692 http://dx.doi.org/10.1186/s13020-023-00717-9 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
An, Yongcheng
Dai, Hongyu
Duan, Yuhui
Cheng, Long
Shi, Lu
He, Changhao
Wang, Chen
Lv, Yinglan
Li, Huimin
Zhang, Huilin
Huang, Yan
Fu, Wanxin
Sun, Weiguang
Zhao, Baosheng
The relationship between gut microbiota and susceptibility to type 2 diabetes mellitus in rats
title The relationship between gut microbiota and susceptibility to type 2 diabetes mellitus in rats
title_full The relationship between gut microbiota and susceptibility to type 2 diabetes mellitus in rats
title_fullStr The relationship between gut microbiota and susceptibility to type 2 diabetes mellitus in rats
title_full_unstemmed The relationship between gut microbiota and susceptibility to type 2 diabetes mellitus in rats
title_short The relationship between gut microbiota and susceptibility to type 2 diabetes mellitus in rats
title_sort relationship between gut microbiota and susceptibility to type 2 diabetes mellitus in rats
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10161507/
https://www.ncbi.nlm.nih.gov/pubmed/37147692
http://dx.doi.org/10.1186/s13020-023-00717-9
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