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Effect of Aging and Glucagon-like Peptide 2 on Intestinal Microbiota in SD Rats

Recent research suggests that intestinal microbiota affect the aging process. Glucagon-like peptide 2 (GLP-2), a growth factor found in the intestinal mucosal epithelium, reduces intestinal permeability and affects intestinal microbiota. The relationship between aging, GLP-2, and intestinal microbio...

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Autores principales: Wu, Jiayu, Ren, Weiying, Li, Li, Luo, Man, Xu, Kan, Shen, Jiping, Wang, Jia, Chang, Guilin, Lu, Yi, Qi, Yiming, Xu, Binger, He, Yuting, Hu, Yu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: JKL International LLC 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6065291/
https://www.ncbi.nlm.nih.gov/pubmed/30090647
http://dx.doi.org/10.14336/AD.2017.1001
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author Wu, Jiayu
Ren, Weiying
Li, Li
Luo, Man
Xu, Kan
Shen, Jiping
Wang, Jia
Chang, Guilin
Lu, Yi
Qi, Yiming
Xu, Binger
He, Yuting
Hu, Yu
author_facet Wu, Jiayu
Ren, Weiying
Li, Li
Luo, Man
Xu, Kan
Shen, Jiping
Wang, Jia
Chang, Guilin
Lu, Yi
Qi, Yiming
Xu, Binger
He, Yuting
Hu, Yu
author_sort Wu, Jiayu
collection PubMed
description Recent research suggests that intestinal microbiota affect the aging process. Glucagon-like peptide 2 (GLP-2), a growth factor found in the intestinal mucosal epithelium, reduces intestinal permeability and affects intestinal microbiota. The relationship between aging, GLP-2, and intestinal microbiota are still not well understood. The current study examined the influence of aging and GLP-2 on the intestinal microbiota of rats. Twelve 3-month old male SD rats were randomly divided into two groups: a young control group (group C) and a young GLP-2 treatment group (group G). Twelve 26-month old male SD rats were randomly divided into two groups: an aged control group (group L) and an aged GLP-2 treatment group (group T). GLP-2 was intraperitoneally injected into rats from group G and group T for 14 days. Plasma GLP-2 concentration was evaluated by ELISA tests. Fresh intestinal stool samples were collected from each group and total fecal bacterial genomic DNA was extracted from the associated rats. The bacterial composition of fecal samples was analyzed by Miseq high-throughput sequencing and comparison with SRA databases. Overall, the diversity of intestinal microbiota significantly decreases with age in SD rats, while GLP-2 has no significant effect on the diversity of intestinal microbiota. Upon aging, there is a reduction in probiotic bacteria and a concomitant increase in pathogenic bacteria in rats. Treatment with GLP-2 results in a significant reduction in the prevalence of pathogenic bacterial genera and an increase in some potential benefit bacteria in aged rats. In addition, treatment with GLP-2 results in an increase in several probiotics and a reduction in the prevalence of pathogenic bacterial genera in young rats.
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spelling pubmed-60652912018-08-08 Effect of Aging and Glucagon-like Peptide 2 on Intestinal Microbiota in SD Rats Wu, Jiayu Ren, Weiying Li, Li Luo, Man Xu, Kan Shen, Jiping Wang, Jia Chang, Guilin Lu, Yi Qi, Yiming Xu, Binger He, Yuting Hu, Yu Aging Dis Orginal Article Recent research suggests that intestinal microbiota affect the aging process. Glucagon-like peptide 2 (GLP-2), a growth factor found in the intestinal mucosal epithelium, reduces intestinal permeability and affects intestinal microbiota. The relationship between aging, GLP-2, and intestinal microbiota are still not well understood. The current study examined the influence of aging and GLP-2 on the intestinal microbiota of rats. Twelve 3-month old male SD rats were randomly divided into two groups: a young control group (group C) and a young GLP-2 treatment group (group G). Twelve 26-month old male SD rats were randomly divided into two groups: an aged control group (group L) and an aged GLP-2 treatment group (group T). GLP-2 was intraperitoneally injected into rats from group G and group T for 14 days. Plasma GLP-2 concentration was evaluated by ELISA tests. Fresh intestinal stool samples were collected from each group and total fecal bacterial genomic DNA was extracted from the associated rats. The bacterial composition of fecal samples was analyzed by Miseq high-throughput sequencing and comparison with SRA databases. Overall, the diversity of intestinal microbiota significantly decreases with age in SD rats, while GLP-2 has no significant effect on the diversity of intestinal microbiota. Upon aging, there is a reduction in probiotic bacteria and a concomitant increase in pathogenic bacteria in rats. Treatment with GLP-2 results in a significant reduction in the prevalence of pathogenic bacterial genera and an increase in some potential benefit bacteria in aged rats. In addition, treatment with GLP-2 results in an increase in several probiotics and a reduction in the prevalence of pathogenic bacterial genera in young rats. JKL International LLC 2018-08-01 /pmc/articles/PMC6065291/ /pubmed/30090647 http://dx.doi.org/10.14336/AD.2017.1001 Text en Copyright: © 2018 Wu et al. http://creativecommons.org/licenses/by/2.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.
spellingShingle Orginal Article
Wu, Jiayu
Ren, Weiying
Li, Li
Luo, Man
Xu, Kan
Shen, Jiping
Wang, Jia
Chang, Guilin
Lu, Yi
Qi, Yiming
Xu, Binger
He, Yuting
Hu, Yu
Effect of Aging and Glucagon-like Peptide 2 on Intestinal Microbiota in SD Rats
title Effect of Aging and Glucagon-like Peptide 2 on Intestinal Microbiota in SD Rats
title_full Effect of Aging and Glucagon-like Peptide 2 on Intestinal Microbiota in SD Rats
title_fullStr Effect of Aging and Glucagon-like Peptide 2 on Intestinal Microbiota in SD Rats
title_full_unstemmed Effect of Aging and Glucagon-like Peptide 2 on Intestinal Microbiota in SD Rats
title_short Effect of Aging and Glucagon-like Peptide 2 on Intestinal Microbiota in SD Rats
title_sort effect of aging and glucagon-like peptide 2 on intestinal microbiota in sd rats
topic Orginal Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6065291/
https://www.ncbi.nlm.nih.gov/pubmed/30090647
http://dx.doi.org/10.14336/AD.2017.1001
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