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Elevated levels of proinflammatory volatile metabolites in feces of high fat diet fed KK-A(y) mice

When the microfloral composition deteriorates, it triggers low-level chronic inflammation associated with several lifestyle-related diseases including obesity and diabetic mellitus. Fecal volatile organic compounds (VOCs) have been found to differ in gastrointestinal diseases as well as intestinal i...

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Autores principales: Uchikawa, Misaki, Kato, Mai, Nagata, Akika, Sanada, Shunsuke, Yoshikawa, Yuto, Tsunematsu, Yuta, Sato, Michio, Suzuki, Takuji, Hashidume, Tsutomu, Watanabe, Kenji, Yoshikawa, Yuko, Miyoshi, Noriyuki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7105489/
https://www.ncbi.nlm.nih.gov/pubmed/32231228
http://dx.doi.org/10.1038/s41598-020-62541-7
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author Uchikawa, Misaki
Kato, Mai
Nagata, Akika
Sanada, Shunsuke
Yoshikawa, Yuto
Tsunematsu, Yuta
Sato, Michio
Suzuki, Takuji
Hashidume, Tsutomu
Watanabe, Kenji
Yoshikawa, Yuko
Miyoshi, Noriyuki
author_facet Uchikawa, Misaki
Kato, Mai
Nagata, Akika
Sanada, Shunsuke
Yoshikawa, Yuto
Tsunematsu, Yuta
Sato, Michio
Suzuki, Takuji
Hashidume, Tsutomu
Watanabe, Kenji
Yoshikawa, Yuko
Miyoshi, Noriyuki
author_sort Uchikawa, Misaki
collection PubMed
description When the microfloral composition deteriorates, it triggers low-level chronic inflammation associated with several lifestyle-related diseases including obesity and diabetic mellitus. Fecal volatile organic compounds (VOCs) have been found to differ in gastrointestinal diseases as well as intestinal infection. In this study, to evaluate a potential association between the pathogenesis of lifestyle-related diseases and VOCs in the intestinal tract, fecal VOCs from obese/diabetic KK-A(y) mice (KK) or controls (C57BL/6J mice; BL) fed a normal or high fat diet (NFD or HFD) were investigated using headspace sampler-GC-EI-MS. Principal component analysis (PCA) of fecal VOC profiles clearly separated the experimental groups depending on the mouse lineage (KK vs BL) and the diet type (NFD vs HFD). 16 s rRNA sequencing revealed that the PCA distribution of VOCs was in parallel with the microfloral composition. We identified that some volatile metabolites including n-alkanals (nonanal and octanal), acetone and phenol were significantly increased in the HFD and/or KK groups. Additionally, these volatile metabolites induced proinflammatory activity in the RAW264 murine macrophage cell line indicating these bioactive metabolites might trigger low-level chronic inflammation. These results suggest that proinflammatory VOCs detected in HFD-fed and/or diabetic model mice might be novel noninvasive diagnosis biomarkers for diabetes.
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spelling pubmed-71054892020-04-06 Elevated levels of proinflammatory volatile metabolites in feces of high fat diet fed KK-A(y) mice Uchikawa, Misaki Kato, Mai Nagata, Akika Sanada, Shunsuke Yoshikawa, Yuto Tsunematsu, Yuta Sato, Michio Suzuki, Takuji Hashidume, Tsutomu Watanabe, Kenji Yoshikawa, Yuko Miyoshi, Noriyuki Sci Rep Article When the microfloral composition deteriorates, it triggers low-level chronic inflammation associated with several lifestyle-related diseases including obesity and diabetic mellitus. Fecal volatile organic compounds (VOCs) have been found to differ in gastrointestinal diseases as well as intestinal infection. In this study, to evaluate a potential association between the pathogenesis of lifestyle-related diseases and VOCs in the intestinal tract, fecal VOCs from obese/diabetic KK-A(y) mice (KK) or controls (C57BL/6J mice; BL) fed a normal or high fat diet (NFD or HFD) were investigated using headspace sampler-GC-EI-MS. Principal component analysis (PCA) of fecal VOC profiles clearly separated the experimental groups depending on the mouse lineage (KK vs BL) and the diet type (NFD vs HFD). 16 s rRNA sequencing revealed that the PCA distribution of VOCs was in parallel with the microfloral composition. We identified that some volatile metabolites including n-alkanals (nonanal and octanal), acetone and phenol were significantly increased in the HFD and/or KK groups. Additionally, these volatile metabolites induced proinflammatory activity in the RAW264 murine macrophage cell line indicating these bioactive metabolites might trigger low-level chronic inflammation. These results suggest that proinflammatory VOCs detected in HFD-fed and/or diabetic model mice might be novel noninvasive diagnosis biomarkers for diabetes. Nature Publishing Group UK 2020-03-30 /pmc/articles/PMC7105489/ /pubmed/32231228 http://dx.doi.org/10.1038/s41598-020-62541-7 Text en © The Author(s) 2020 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Uchikawa, Misaki
Kato, Mai
Nagata, Akika
Sanada, Shunsuke
Yoshikawa, Yuto
Tsunematsu, Yuta
Sato, Michio
Suzuki, Takuji
Hashidume, Tsutomu
Watanabe, Kenji
Yoshikawa, Yuko
Miyoshi, Noriyuki
Elevated levels of proinflammatory volatile metabolites in feces of high fat diet fed KK-A(y) mice
title Elevated levels of proinflammatory volatile metabolites in feces of high fat diet fed KK-A(y) mice
title_full Elevated levels of proinflammatory volatile metabolites in feces of high fat diet fed KK-A(y) mice
title_fullStr Elevated levels of proinflammatory volatile metabolites in feces of high fat diet fed KK-A(y) mice
title_full_unstemmed Elevated levels of proinflammatory volatile metabolites in feces of high fat diet fed KK-A(y) mice
title_short Elevated levels of proinflammatory volatile metabolites in feces of high fat diet fed KK-A(y) mice
title_sort elevated levels of proinflammatory volatile metabolites in feces of high fat diet fed kk-a(y) mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7105489/
https://www.ncbi.nlm.nih.gov/pubmed/32231228
http://dx.doi.org/10.1038/s41598-020-62541-7
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