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Alpha-ketoglutarate (AKG) lowers body weight and affects intestinal innate immunity through influencing intestinal microbiota

Alpha-ketoglutarate (AKG), a precursor of glutamate and a critical intermediate in the tricarboxylic acid cycle, shows beneficial effects on intestinal function. However, the influence of AKG on the intestinal innate immune system and intestinal microbiota is unknown. This study explores the effect...

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Autores principales: Chen, Shuai, Bin, Peng, Ren, Wenkai, Gao, Wei, Liu, Gang, Yin, Jie, Duan, Jielin, Li, Yinghui, Yao, Kang, Huang, Ruilin, Tan, Bie, Yin, Yulong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5503525/
https://www.ncbi.nlm.nih.gov/pubmed/28465471
http://dx.doi.org/10.18632/oncotarget.17132
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author Chen, Shuai
Bin, Peng
Ren, Wenkai
Gao, Wei
Liu, Gang
Yin, Jie
Duan, Jielin
Li, Yinghui
Yao, Kang
Huang, Ruilin
Tan, Bie
Yin, Yulong
author_facet Chen, Shuai
Bin, Peng
Ren, Wenkai
Gao, Wei
Liu, Gang
Yin, Jie
Duan, Jielin
Li, Yinghui
Yao, Kang
Huang, Ruilin
Tan, Bie
Yin, Yulong
author_sort Chen, Shuai
collection PubMed
description Alpha-ketoglutarate (AKG), a precursor of glutamate and a critical intermediate in the tricarboxylic acid cycle, shows beneficial effects on intestinal function. However, the influence of AKG on the intestinal innate immune system and intestinal microbiota is unknown. This study explores the effect of oral AKG administration in drinking water (10 g/L) on intestinal innate immunity and intestinal microbiota in a mouse model. Mouse water intake, feed intake and body weight were recorded throughout the entire experiment. The ileum was collected for detecting the expression of intestinal proinflammatory cytokines and innate immune factors by Real-time Polymerase Chain Reaction. Additionally, the ileal luminal contents and feces were collected for 16S rDNA sequencing to analyze the microbial composition. The intestinal microbiota in mice was disrupted with an antibiotic cocktail. The results revealed that AKG supplementation lowered body weight, promoted ileal expression of mammalian defensins of the alpha subfamily (such as cryptdins-1, cryptdins-4, and cryptdins-5) while influencing the intestinal microbial composition (i.e., lowering the Firmicutes to Bacteroidetes ratio). In the antibiotic-treated mouse model, AKG supplementation failed to affect mouse body weight and inhibited the expression of cryptdins-1 and cryptdins-5 in the ileum. We concluded that AKG might affect body weight and intestinal innate immunity through influencing intestinal microbiota.
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spelling pubmed-55035252017-07-11 Alpha-ketoglutarate (AKG) lowers body weight and affects intestinal innate immunity through influencing intestinal microbiota Chen, Shuai Bin, Peng Ren, Wenkai Gao, Wei Liu, Gang Yin, Jie Duan, Jielin Li, Yinghui Yao, Kang Huang, Ruilin Tan, Bie Yin, Yulong Oncotarget Research Paper: Pathology Alpha-ketoglutarate (AKG), a precursor of glutamate and a critical intermediate in the tricarboxylic acid cycle, shows beneficial effects on intestinal function. However, the influence of AKG on the intestinal innate immune system and intestinal microbiota is unknown. This study explores the effect of oral AKG administration in drinking water (10 g/L) on intestinal innate immunity and intestinal microbiota in a mouse model. Mouse water intake, feed intake and body weight were recorded throughout the entire experiment. The ileum was collected for detecting the expression of intestinal proinflammatory cytokines and innate immune factors by Real-time Polymerase Chain Reaction. Additionally, the ileal luminal contents and feces were collected for 16S rDNA sequencing to analyze the microbial composition. The intestinal microbiota in mice was disrupted with an antibiotic cocktail. The results revealed that AKG supplementation lowered body weight, promoted ileal expression of mammalian defensins of the alpha subfamily (such as cryptdins-1, cryptdins-4, and cryptdins-5) while influencing the intestinal microbial composition (i.e., lowering the Firmicutes to Bacteroidetes ratio). In the antibiotic-treated mouse model, AKG supplementation failed to affect mouse body weight and inhibited the expression of cryptdins-1 and cryptdins-5 in the ileum. We concluded that AKG might affect body weight and intestinal innate immunity through influencing intestinal microbiota. Impact Journals LLC 2017-04-16 /pmc/articles/PMC5503525/ /pubmed/28465471 http://dx.doi.org/10.18632/oncotarget.17132 Text en Copyright: © 2017 Chen et al. http://creativecommons.org/licenses/by/3.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) (CC-BY), which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Research Paper: Pathology
Chen, Shuai
Bin, Peng
Ren, Wenkai
Gao, Wei
Liu, Gang
Yin, Jie
Duan, Jielin
Li, Yinghui
Yao, Kang
Huang, Ruilin
Tan, Bie
Yin, Yulong
Alpha-ketoglutarate (AKG) lowers body weight and affects intestinal innate immunity through influencing intestinal microbiota
title Alpha-ketoglutarate (AKG) lowers body weight and affects intestinal innate immunity through influencing intestinal microbiota
title_full Alpha-ketoglutarate (AKG) lowers body weight and affects intestinal innate immunity through influencing intestinal microbiota
title_fullStr Alpha-ketoglutarate (AKG) lowers body weight and affects intestinal innate immunity through influencing intestinal microbiota
title_full_unstemmed Alpha-ketoglutarate (AKG) lowers body weight and affects intestinal innate immunity through influencing intestinal microbiota
title_short Alpha-ketoglutarate (AKG) lowers body weight and affects intestinal innate immunity through influencing intestinal microbiota
title_sort alpha-ketoglutarate (akg) lowers body weight and affects intestinal innate immunity through influencing intestinal microbiota
topic Research Paper: Pathology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5503525/
https://www.ncbi.nlm.nih.gov/pubmed/28465471
http://dx.doi.org/10.18632/oncotarget.17132
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