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Impact of habitual chewing on gut motility via microbiota transition

The gut environment, including the microbiota and its metabolites and short-chain fatty acids (SCFA), is essential for health maintenance. It is considered that functional recovery treatment for masticatory dysphagia affects the composition of the gut microbiota, indicating that habitual mastication...

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Autores principales: Yaoita, Fukie, Watanabe, Keita, Kimura, Ikuo, Miyazawa, Masayuki, Tsuchiya, Shinobu, Kanzaki, Makoto, Tsuchiya, Masahiro, Tan-No, Koichi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9378666/
https://www.ncbi.nlm.nih.gov/pubmed/35970869
http://dx.doi.org/10.1038/s41598-022-18095-x
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author Yaoita, Fukie
Watanabe, Keita
Kimura, Ikuo
Miyazawa, Masayuki
Tsuchiya, Shinobu
Kanzaki, Makoto
Tsuchiya, Masahiro
Tan-No, Koichi
author_facet Yaoita, Fukie
Watanabe, Keita
Kimura, Ikuo
Miyazawa, Masayuki
Tsuchiya, Shinobu
Kanzaki, Makoto
Tsuchiya, Masahiro
Tan-No, Koichi
author_sort Yaoita, Fukie
collection PubMed
description The gut environment, including the microbiota and its metabolites and short-chain fatty acids (SCFA), is essential for health maintenance. It is considered that functional recovery treatment for masticatory dysphagia affects the composition of the gut microbiota, indicating that habitual mastication, depending on the hardness of the food, may affect the gut microbiota and environment. However, the impact of chronic powdered diet feeding on the colonic condition and motility remains unclear. Here, we evaluated various colonic features in mice fed with powdered diets for a long-term and a mouse model with masticatory behavior. We observed a decreased abundance of the SCFA-producing bacterial genera in the ceca of the powdered diet-fed mice. Based on the importance of SCFAs in gut immune homeostasis and motility, interestingly, powdered diet feeding also resulted in constipation-like symptoms due to mild colitis, which were ameliorated by the administration of a neutrophil-depleting agent and neutrophil elastase inhibitors. Lastly, the suppressed colonic motility in the powdered diet-fed mice was significantly improved by loading masticatory activity for 2 h. Thus, feeding habits with appropriate masticatory activity and stimulation may play a key role in providing a favorable gut environment based on interactions between the gut microbiota and host immune system.
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spelling pubmed-93786662022-08-17 Impact of habitual chewing on gut motility via microbiota transition Yaoita, Fukie Watanabe, Keita Kimura, Ikuo Miyazawa, Masayuki Tsuchiya, Shinobu Kanzaki, Makoto Tsuchiya, Masahiro Tan-No, Koichi Sci Rep Article The gut environment, including the microbiota and its metabolites and short-chain fatty acids (SCFA), is essential for health maintenance. It is considered that functional recovery treatment for masticatory dysphagia affects the composition of the gut microbiota, indicating that habitual mastication, depending on the hardness of the food, may affect the gut microbiota and environment. However, the impact of chronic powdered diet feeding on the colonic condition and motility remains unclear. Here, we evaluated various colonic features in mice fed with powdered diets for a long-term and a mouse model with masticatory behavior. We observed a decreased abundance of the SCFA-producing bacterial genera in the ceca of the powdered diet-fed mice. Based on the importance of SCFAs in gut immune homeostasis and motility, interestingly, powdered diet feeding also resulted in constipation-like symptoms due to mild colitis, which were ameliorated by the administration of a neutrophil-depleting agent and neutrophil elastase inhibitors. Lastly, the suppressed colonic motility in the powdered diet-fed mice was significantly improved by loading masticatory activity for 2 h. Thus, feeding habits with appropriate masticatory activity and stimulation may play a key role in providing a favorable gut environment based on interactions between the gut microbiota and host immune system. Nature Publishing Group UK 2022-08-15 /pmc/articles/PMC9378666/ /pubmed/35970869 http://dx.doi.org/10.1038/s41598-022-18095-x Text en © The Author(s) 2022 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
Yaoita, Fukie
Watanabe, Keita
Kimura, Ikuo
Miyazawa, Masayuki
Tsuchiya, Shinobu
Kanzaki, Makoto
Tsuchiya, Masahiro
Tan-No, Koichi
Impact of habitual chewing on gut motility via microbiota transition
title Impact of habitual chewing on gut motility via microbiota transition
title_full Impact of habitual chewing on gut motility via microbiota transition
title_fullStr Impact of habitual chewing on gut motility via microbiota transition
title_full_unstemmed Impact of habitual chewing on gut motility via microbiota transition
title_short Impact of habitual chewing on gut motility via microbiota transition
title_sort impact of habitual chewing on gut motility via microbiota transition
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9378666/
https://www.ncbi.nlm.nih.gov/pubmed/35970869
http://dx.doi.org/10.1038/s41598-022-18095-x
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