Barley β-glucan consumption improves glucose tolerance by increasing intestinal succinate concentrations

Barley is rich in β-glucan, which can alter gut microbiota and metabolome profiles, potentially affecting host metabolism. However, the microbiota and metabolites increased by barley β-glucan remain unclear. In this study, we focused on the gut-microbiota-derived metabolite succinate and investigated the microbiome and metabolome profiles altered by barley β-glucan intake. C57BL/6 J mice were fed a standard or middle-fat diet containing barley flour rich in β-glucan or barley flour without β-glucan, and their gut microbiota and metabolome profiles were analyzed. The results showed increased Bacteroides, Parasutterella, and succinate due to barley β-glucan intake independent of diet differences. Next, we used mice lacking slc13a2, a gene that is involved in the cellular uptake of succinate. Wild-type mice showed improved glucose tolerance after the intake of barley β-glucan, but this effect was attenuated in the slc13a2-deficient mice. These results suggest that barley β-glucan intake increases succinate and succinate-producing bacteria and affects glucose metabolism.

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Publication Details

Journal
npj Science of Food
Published
2024-09-30
DOI
https://doi.org/10.1038/s41538-024-00311-9
Citations
8
Primary Topic
Food composition and properties
Type
article
Field-Weighted Citation Impact
2.48

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article

Barley β-glucan consumption improves glucose tolerance by increasing intestinal succinate concentrations

Kento Mio, Tsubasa Matsuoka, Seiichiro Aoe, Toshiki Kobayashi et al.
8 citations
npj Science of Food
Food composition and properties
2.48
article

Barley β-glucan consumption improves glucose tolerance by increasing intestinal succinate concentrations

Kento Mio, Tsubasa Matsuoka, Seiichiro Aoe, Toshiki Kobayashi, Jiayue Yang, Yuka Goto, Shinji Fukuda, Chiharu Ishii, Mitsuko Komatsu
article en
8 citations

Abstract

Barley is rich in β-glucan, which can alter gut microbiota and metabolome profiles, potentially affecting host metabolism. However, the microbiota and metabolites increased by barley β-glucan remain unclear. In this study, we focused on the gut-microbiota-derived metabolite succinate and investigated the microbiome and metabolome profiles altered by barley β-glucan intake. C57BL/6 J mice were fed a standard or middle-fat diet containing barley flour rich in β-glucan or barley flour without β-glucan, and their gut microbiota and metabolome profiles were analyzed. The results showed increased Bacteroides, Parasutterella, and succinate due to barley β-glucan intake independent of diet differences. Next, we used mice lacking slc13a2, a gene that is involved in the cellular uptake of succinate. Wild-type mice showed improved glucose tolerance after the intake of barley β-glucan, but this effect was attenuated in the slc13a2-deficient mice. These results suggest that barley β-glucan intake increases succinate and succinate-producing bacteria and affects glucose metabolism.

npj Science of FoodVol. 8(1)
Yamagata University (JP), Hakuoh University (JP), University of Tsukuba (JP), Otsuma Women's University (JP), Keio University (JP), Juntendo University (JP), Kanagawa Industrial Technology Center (JP), University of Yamanashi (JP)
Japan Agency for Medical Research and Development, Keio University, Japan Society for the Promotion of Science, Core Research for Evolutional Science and Technology, Exploratory Research for Advanced Technology
Zero hunger
Openalex Percentile: Top 11%
Food composition and properties
2.48
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