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Profiling of Polar Metabolites in Mouse Feces Using Four Analytical Platforms to Study the Effects Of Cathelicidin-Related Antimicrobial Peptide in Alcoholic Liver Disease

Identifieur interne : 000517 ( Main/Exploration ); précédent : 000516; suivant : 000518

Profiling of Polar Metabolites in Mouse Feces Using Four Analytical Platforms to Study the Effects Of Cathelicidin-Related Antimicrobial Peptide in Alcoholic Liver Disease

Auteurs : Liqing He [États-Unis] ; Fengyuan Li [États-Unis] ; Xinmin Yin [États-Unis] ; Patrick Bohman [États-Unis] ; Seongho Kim [États-Unis] ; Craig J. Mcclain [États-Unis] ; Wenke Feng [États-Unis] ; Xiang Zhang [États-Unis]

Source :

RBID : PMC:6748645

Abstract

Alterations in gut bacterial homeostasis result in changes in intestinal metabolites. To investigate the effects of alcohol on fecal metabolites and the role of cathelicidin-related antimicrobial peptide (CRAMP) in alcoholic liver disease (ALD), CRAMP knockout (KO) and their control wild type (WT) mice were fed a Lieber-DeCarli liquid diet with or without alcohol. Polar metabolites in mouse feces were analyzed by GC × GC-MS and 2DLC-MS, and the concentrations of short chain fatty acids (SCFAs) were measured by GC-MS. A total of 95 and 190 metabolites were detected by GC × GC-MS and 2DLC-MS, respectively. Among the significantly changed metabolites, taurine and nicotinic acid were decreased in WT mice fed alcohol, which were also down-regulated in KO mice fed without alcohol. Interestingly, these two metabolites were increased in KO mice fed alcohol compared to them in WT controls. Additionally, SCFAs were significantly decreased in WT mice fed alcohol and in KO mice fed without alcohol, whereas two branched-chain SCFAs were increased by alcohol treatment in KO mice. In summary, the analytical platforms employed in this study successfully dissected the alterations of polar metabolites and SCFAs in fecal samples, which helped understand the effects of alcohol consumption and CRAMP in intestinal metabolism and alcohol-induced liver injury.


Url:
DOI: 10.1021/acs.jproteome.9b00181
PubMed: 31188604
PubMed Central: 6748645


Affiliations:


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Le document en format XML

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<name sortKey="Feng, Wenke" sort="Feng, Wenke" uniqKey="Feng W" first="Wenke" last="Feng">Wenke Feng</name>
<affiliation wicri:level="1">
<nlm:aff id="A2">University of Louisville Alcohol Research Center, University of Louisville, Louisville, Kentucky 40208, United States</nlm:aff>
<country xml:lang="fr">États-Unis</country>
<wicri:regionArea>University of Louisville Alcohol Research Center, University of Louisville, Louisville, Kentucky 40208</wicri:regionArea>
<wicri:noRegion>Kentucky 40208</wicri:noRegion>
</affiliation>
<affiliation wicri:level="1">
<nlm:aff id="A3">University of Louisville Hepatobiology & Toxicology Center, University of Louisville, Louisville, Kentucky 40208, United States</nlm:aff>
<country xml:lang="fr">États-Unis</country>
<wicri:regionArea>University of Louisville Hepatobiology & Toxicology Center, University of Louisville, Louisville, Kentucky 40208</wicri:regionArea>
<wicri:noRegion>Kentucky 40208</wicri:noRegion>
</affiliation>
<affiliation wicri:level="1">
<nlm:aff id="A4">Center for Regulatory and Environmental Analytical Metabolomics, University of Louisville, Louisville, Kentucky 40208, United States</nlm:aff>
<country xml:lang="fr">États-Unis</country>
<wicri:regionArea>Center for Regulatory and Environmental Analytical Metabolomics, University of Louisville, Louisville, Kentucky 40208</wicri:regionArea>
<wicri:noRegion>Kentucky 40208</wicri:noRegion>
</affiliation>
<affiliation wicri:level="1">
<nlm:aff id="A5">Department of Pharmacology & Toxicology, University of Louisville, Louisville, Kentucky 40208, United States</nlm:aff>
<country xml:lang="fr">États-Unis</country>
<wicri:regionArea>Department of Pharmacology & Toxicology, University of Louisville, Louisville, Kentucky 40208</wicri:regionArea>
<wicri:noRegion>Kentucky 40208</wicri:noRegion>
</affiliation>
<affiliation wicri:level="1">
<nlm:aff id="A6">Department of Medicine, University of Louisville, Louisville, Kentucky 40208, United States</nlm:aff>
<country xml:lang="fr">États-Unis</country>
<wicri:regionArea>Department of Medicine, University of Louisville, Louisville, Kentucky 40208</wicri:regionArea>
<wicri:noRegion>Kentucky 40208</wicri:noRegion>
</affiliation>
</author>
<author>
<name sortKey="Zhang, Xiang" sort="Zhang, Xiang" uniqKey="Zhang X" first="Xiang" last="Zhang">Xiang Zhang</name>
<affiliation wicri:level="1">
<nlm:aff id="A1">Department of Chemistry, University of Louisville, Louisville, Kentucky 40208, United States</nlm:aff>
<country xml:lang="fr">États-Unis</country>
<wicri:regionArea>Department of Chemistry, University of Louisville, Louisville, Kentucky 40208</wicri:regionArea>
<wicri:noRegion>Kentucky 40208</wicri:noRegion>
</affiliation>
<affiliation wicri:level="1">
<nlm:aff id="A2">University of Louisville Alcohol Research Center, University of Louisville, Louisville, Kentucky 40208, United States</nlm:aff>
<country xml:lang="fr">États-Unis</country>
<wicri:regionArea>University of Louisville Alcohol Research Center, University of Louisville, Louisville, Kentucky 40208</wicri:regionArea>
<wicri:noRegion>Kentucky 40208</wicri:noRegion>
</affiliation>
<affiliation wicri:level="1">
<nlm:aff id="A3">University of Louisville Hepatobiology & Toxicology Center, University of Louisville, Louisville, Kentucky 40208, United States</nlm:aff>
<country xml:lang="fr">États-Unis</country>
<wicri:regionArea>University of Louisville Hepatobiology & Toxicology Center, University of Louisville, Louisville, Kentucky 40208</wicri:regionArea>
<wicri:noRegion>Kentucky 40208</wicri:noRegion>
</affiliation>
<affiliation wicri:level="1">
<nlm:aff id="A4">Center for Regulatory and Environmental Analytical Metabolomics, University of Louisville, Louisville, Kentucky 40208, United States</nlm:aff>
<country xml:lang="fr">États-Unis</country>
<wicri:regionArea>Center for Regulatory and Environmental Analytical Metabolomics, University of Louisville, Louisville, Kentucky 40208</wicri:regionArea>
<wicri:noRegion>Kentucky 40208</wicri:noRegion>
</affiliation>
<affiliation wicri:level="1">
<nlm:aff id="A5">Department of Pharmacology & Toxicology, University of Louisville, Louisville, Kentucky 40208, United States</nlm:aff>
<country xml:lang="fr">États-Unis</country>
<wicri:regionArea>Department of Pharmacology & Toxicology, University of Louisville, Louisville, Kentucky 40208</wicri:regionArea>
<wicri:noRegion>Kentucky 40208</wicri:noRegion>
</affiliation>
</author>
</analytic>
<series>
<title level="j">Journal of proteome research</title>
<idno type="ISSN">1535-3893</idno>
<idno type="eISSN">1535-3907</idno>
<imprint>
<date when="2019">2019</date>
</imprint>
</series>
</biblStruct>
</sourceDesc>
</fileDesc>
<profileDesc>
<textClass></textClass>
</profileDesc>
</teiHeader>
<front>
<div type="abstract" xml:lang="en">
<p id="P1">Alterations in gut bacterial homeostasis result in changes in intestinal metabolites. To investigate the effects of alcohol on fecal metabolites and the role of cathelicidin-related antimicrobial peptide (CRAMP) in alcoholic liver disease (ALD), CRAMP knockout (KO) and their control wild type (WT) mice were fed a Lieber-DeCarli liquid diet with or without alcohol. Polar metabolites in mouse feces were analyzed by GC × GC-MS and 2DLC-MS, and the concentrations of short chain fatty acids (SCFAs) were measured by GC-MS. A total of 95 and 190 metabolites were detected by GC × GC-MS and 2DLC-MS, respectively. Among the significantly changed metabolites, taurine and nicotinic acid were decreased in WT mice fed alcohol, which were also down-regulated in KO mice fed without alcohol. Interestingly, these two metabolites were increased in KO mice fed alcohol compared to them in WT controls. Additionally, SCFAs were significantly decreased in WT mice fed alcohol and in KO mice fed without alcohol, whereas two branched-chain SCFAs were increased by alcohol treatment in KO mice. In summary, the analytical platforms employed in this study successfully dissected the alterations of polar metabolites and SCFAs in fecal samples, which helped understand the effects of alcohol consumption and CRAMP in intestinal metabolism and alcohol-induced liver injury.</p>
</div>
</front>
</TEI>
<affiliations>
<list>
<country>
<li>États-Unis</li>
</country>
</list>
<tree>
<country name="États-Unis">
<noRegion>
<name sortKey="He, Liqing" sort="He, Liqing" uniqKey="He L" first="Liqing" last="He">Liqing He</name>
</noRegion>
<name sortKey="Bohman, Patrick" sort="Bohman, Patrick" uniqKey="Bohman P" first="Patrick" last="Bohman">Patrick Bohman</name>
<name sortKey="Feng, Wenke" sort="Feng, Wenke" uniqKey="Feng W" first="Wenke" last="Feng">Wenke Feng</name>
<name sortKey="Feng, Wenke" sort="Feng, Wenke" uniqKey="Feng W" first="Wenke" last="Feng">Wenke Feng</name>
<name sortKey="Feng, Wenke" sort="Feng, Wenke" uniqKey="Feng W" first="Wenke" last="Feng">Wenke Feng</name>
<name sortKey="Feng, Wenke" sort="Feng, Wenke" uniqKey="Feng W" first="Wenke" last="Feng">Wenke Feng</name>
<name sortKey="Feng, Wenke" sort="Feng, Wenke" uniqKey="Feng W" first="Wenke" last="Feng">Wenke Feng</name>
<name sortKey="He, Liqing" sort="He, Liqing" uniqKey="He L" first="Liqing" last="He">Liqing He</name>
<name sortKey="He, Liqing" sort="He, Liqing" uniqKey="He L" first="Liqing" last="He">Liqing He</name>
<name sortKey="He, Liqing" sort="He, Liqing" uniqKey="He L" first="Liqing" last="He">Liqing He</name>
<name sortKey="Kim, Seongho" sort="Kim, Seongho" uniqKey="Kim S" first="Seongho" last="Kim">Seongho Kim</name>
<name sortKey="Li, Fengyuan" sort="Li, Fengyuan" uniqKey="Li F" first="Fengyuan" last="Li">Fengyuan Li</name>
<name sortKey="Li, Fengyuan" sort="Li, Fengyuan" uniqKey="Li F" first="Fengyuan" last="Li">Fengyuan Li</name>
<name sortKey="Li, Fengyuan" sort="Li, Fengyuan" uniqKey="Li F" first="Fengyuan" last="Li">Fengyuan Li</name>
<name sortKey="Mcclain, Craig J" sort="Mcclain, Craig J" uniqKey="Mcclain C" first="Craig J." last="Mcclain">Craig J. Mcclain</name>
<name sortKey="Mcclain, Craig J" sort="Mcclain, Craig J" uniqKey="Mcclain C" first="Craig J." last="Mcclain">Craig J. Mcclain</name>
<name sortKey="Mcclain, Craig J" sort="Mcclain, Craig J" uniqKey="Mcclain C" first="Craig J." last="Mcclain">Craig J. Mcclain</name>
<name sortKey="Mcclain, Craig J" sort="Mcclain, Craig J" uniqKey="Mcclain C" first="Craig J." last="Mcclain">Craig J. Mcclain</name>
<name sortKey="Mcclain, Craig J" sort="Mcclain, Craig J" uniqKey="Mcclain C" first="Craig J." last="Mcclain">Craig J. Mcclain</name>
<name sortKey="Yin, Xinmin" sort="Yin, Xinmin" uniqKey="Yin X" first="Xinmin" last="Yin">Xinmin Yin</name>
<name sortKey="Yin, Xinmin" sort="Yin, Xinmin" uniqKey="Yin X" first="Xinmin" last="Yin">Xinmin Yin</name>
<name sortKey="Yin, Xinmin" sort="Yin, Xinmin" uniqKey="Yin X" first="Xinmin" last="Yin">Xinmin Yin</name>
<name sortKey="Yin, Xinmin" sort="Yin, Xinmin" uniqKey="Yin X" first="Xinmin" last="Yin">Xinmin Yin</name>
<name sortKey="Zhang, Xiang" sort="Zhang, Xiang" uniqKey="Zhang X" first="Xiang" last="Zhang">Xiang Zhang</name>
<name sortKey="Zhang, Xiang" sort="Zhang, Xiang" uniqKey="Zhang X" first="Xiang" last="Zhang">Xiang Zhang</name>
<name sortKey="Zhang, Xiang" sort="Zhang, Xiang" uniqKey="Zhang X" first="Xiang" last="Zhang">Xiang Zhang</name>
<name sortKey="Zhang, Xiang" sort="Zhang, Xiang" uniqKey="Zhang X" first="Xiang" last="Zhang">Xiang Zhang</name>
<name sortKey="Zhang, Xiang" sort="Zhang, Xiang" uniqKey="Zhang X" first="Xiang" last="Zhang">Xiang Zhang</name>
</country>
</tree>
</affiliations>
</record>

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