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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creator | Uchikawa, Misaki Kato, Mai Nagata, Akika Sanada, Shunsuke Yoshikawa, Yuto Tsunematsu, Yuta Sato, Michio Suzuki, Takuji Hashidume, Tsutomu Watanabe, Kenji Yoshikawa, Yuko Miyoshi, Noriyuki |
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
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. |
doi_str_mv | 10.1038/s41598-020-62541-7 |
format | Article |
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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.</description><identifier>EISSN: 2045-2322</identifier><identifier>DOI: 10.1038/s41598-020-62541-7</identifier><identifier>PMID: 32231228</identifier><language>eng</language><publisher>England</publisher><subject>Animals ; Biomarkers - analysis ; Diet, High-Fat - adverse effects ; Disease Models, Animal ; Feces - chemistry ; Gastrointestinal Microbiome - genetics ; Inflammation ; Male ; Mice ; Mice, Inbred C57BL ; Mice, Obese ; Obesity - metabolism ; RAW 264.7 Cells ; RNA, Ribosomal, 16S - genetics ; Volatile Organic Compounds - analysis</subject><ispartof>Scientific reports, 2020-03, Vol.10 (1), p.5681</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,860,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32231228$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Uchikawa, Misaki</creatorcontrib><creatorcontrib>Kato, Mai</creatorcontrib><creatorcontrib>Nagata, Akika</creatorcontrib><creatorcontrib>Sanada, Shunsuke</creatorcontrib><creatorcontrib>Yoshikawa, Yuto</creatorcontrib><creatorcontrib>Tsunematsu, Yuta</creatorcontrib><creatorcontrib>Sato, Michio</creatorcontrib><creatorcontrib>Suzuki, Takuji</creatorcontrib><creatorcontrib>Hashidume, Tsutomu</creatorcontrib><creatorcontrib>Watanabe, Kenji</creatorcontrib><creatorcontrib>Yoshikawa, Yuko</creatorcontrib><creatorcontrib>Miyoshi, Noriyuki</creatorcontrib><title>Elevated levels of proinflammatory volatile metabolites in feces of high fat diet fed KK-A y mice</title><title>Scientific reports</title><addtitle>Sci Rep</addtitle><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
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.</description><subject>Animals</subject><subject>Biomarkers - analysis</subject><subject>Diet, High-Fat - adverse effects</subject><subject>Disease Models, Animal</subject><subject>Feces - chemistry</subject><subject>Gastrointestinal Microbiome - genetics</subject><subject>Inflammation</subject><subject>Male</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Mice, Obese</subject><subject>Obesity - metabolism</subject><subject>RAW 264.7 Cells</subject><subject>RNA, Ribosomal, 16S - genetics</subject><subject>Volatile Organic Compounds - analysis</subject><issn>2045-2322</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFjsGKwjAURcOAjKL-gIvh_UA0eW1n2uUgiuDWfXnalzGSmNJkhP69RXTt3Rw43AtXiIVWS62ychVzXVSlVKjkNxa5lj8fYoIqLyRmiGMxj_GihhRY5br6FOPBZhqxnAjaOL5R4gYGsosQDLRdsFfjyHtKoevhFhwl6xg8JzoGZxNHsFcwfOLH4Gz_zmAoQWM5DbqB_V7-Qg_enngmRoZc5PmTU_G13RzWO9n-Hz03ddtZT11fvz5lbwt3u25Hww</recordid><startdate>20200330</startdate><enddate>20200330</enddate><creator>Uchikawa, Misaki</creator><creator>Kato, Mai</creator><creator>Nagata, Akika</creator><creator>Sanada, Shunsuke</creator><creator>Yoshikawa, Yuto</creator><creator>Tsunematsu, Yuta</creator><creator>Sato, Michio</creator><creator>Suzuki, Takuji</creator><creator>Hashidume, Tsutomu</creator><creator>Watanabe, Kenji</creator><creator>Yoshikawa, Yuko</creator><creator>Miyoshi, Noriyuki</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope></search><sort><creationdate>20200330</creationdate><title>Elevated levels of proinflammatory volatile metabolites in feces of high fat diet fed KK-A y mice</title><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></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-pubmed_primary_322312283</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Animals</topic><topic>Biomarkers - analysis</topic><topic>Diet, High-Fat - adverse effects</topic><topic>Disease Models, Animal</topic><topic>Feces - chemistry</topic><topic>Gastrointestinal Microbiome - genetics</topic><topic>Inflammation</topic><topic>Male</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Mice, Obese</topic><topic>Obesity - metabolism</topic><topic>RAW 264.7 Cells</topic><topic>RNA, Ribosomal, 16S - genetics</topic><topic>Volatile Organic Compounds - analysis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Uchikawa, Misaki</creatorcontrib><creatorcontrib>Kato, Mai</creatorcontrib><creatorcontrib>Nagata, Akika</creatorcontrib><creatorcontrib>Sanada, Shunsuke</creatorcontrib><creatorcontrib>Yoshikawa, Yuto</creatorcontrib><creatorcontrib>Tsunematsu, Yuta</creatorcontrib><creatorcontrib>Sato, Michio</creatorcontrib><creatorcontrib>Suzuki, Takuji</creatorcontrib><creatorcontrib>Hashidume, Tsutomu</creatorcontrib><creatorcontrib>Watanabe, Kenji</creatorcontrib><creatorcontrib>Yoshikawa, Yuko</creatorcontrib><creatorcontrib>Miyoshi, Noriyuki</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><jtitle>Scientific reports</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Uchikawa, Misaki</au><au>Kato, Mai</au><au>Nagata, Akika</au><au>Sanada, Shunsuke</au><au>Yoshikawa, Yuto</au><au>Tsunematsu, Yuta</au><au>Sato, Michio</au><au>Suzuki, Takuji</au><au>Hashidume, Tsutomu</au><au>Watanabe, Kenji</au><au>Yoshikawa, Yuko</au><au>Miyoshi, Noriyuki</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Elevated levels of proinflammatory volatile metabolites in feces of high fat diet fed KK-A y mice</atitle><jtitle>Scientific reports</jtitle><addtitle>Sci Rep</addtitle><date>2020-03-30</date><risdate>2020</risdate><volume>10</volume><issue>1</issue><spage>5681</spage><pages>5681-</pages><eissn>2045-2322</eissn><abstract>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
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.</abstract><cop>England</cop><pmid>32231228</pmid><doi>10.1038/s41598-020-62541-7</doi></addata></record> |
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subjects | Animals Biomarkers - analysis Diet, High-Fat - adverse effects Disease Models, Animal Feces - chemistry Gastrointestinal Microbiome - genetics Inflammation Male Mice Mice, Inbred C57BL Mice, Obese Obesity - metabolism RAW 264.7 Cells RNA, Ribosomal, 16S - genetics Volatile Organic Compounds - analysis |
title | Elevated levels of proinflammatory volatile metabolites in feces of high fat diet fed KK-A y mice |
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