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  6. Keywords
  7. Topics
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We are analyzing https://link.springer.com/article/10.1186/s13073-016-0296-x.

Title:
Microbial metabolism of dietary components to bioactive metabolites: opportunities for new therapeutic interventions | Genome Medicine
Description:
Mass spectrometry- and nuclear magnetic resonance-based metabolomic studies comparing diseased versus healthy individuals have shown that microbial metabolites are often the compounds most markedly altered in the disease state. Recent studies suggest that several of these metabolites that derive from microbial transformation of dietary components have significant effects on physiological processes such as gut and immune homeostasis, energy metabolism, vascular function, and neurological behavior. Here, we review several of the most intriguing diet-dependent metabolites that may impact host physiology and may therefore be appropriate targets for therapeutic interventions, such as short-chain fatty acids, trimethylamine N-oxide, tryptophan and tyrosine derivatives, and oxidized fatty acids. Such interventions will require modulating either bacterial species or the bacterial biosynthetic enzymes required to produce these metabolites, so we briefly describe the current understanding of the bacterial and enzymatic pathways involved in their biosynthesis and summarize their molecular mechanisms of action. We then discuss in more detail the impact of these metabolites on health and disease, and review current strategies to modulate levels of these metabolites to promote human health. We also suggest future studies that are needed to realize the full therapeutic potential of targeting the gut microbiota.
Website Age:
28 years and 1 months (reg. 1997-05-29).

Matching Content Categories {๐Ÿ“š}

  • Health & Fitness
  • Science
  • Education

Content Management System {๐Ÿ“}

What CMS is link.springer.com built with?

Custom-built

No common CMS systems were detected on Link.springer.com, and no known web development framework was identified.

Traffic Estimate {๐Ÿ“ˆ}

What is the average monthly size of link.springer.com audience?

๐ŸŒ  Phenomenal Traffic: 5M - 10M visitors per month


Based on our best estimate, this website will receive around 7,603,724 visitors per month in the current month.

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How Does Link.springer.com Make Money? {๐Ÿ’ธ}

We donโ€™t know how the website earns money.

While many websites aim to make money, others are created to share knowledge or showcase creativity. People build websites for various reasons. This could be one of them. Link.springer.com might be making money, but it's not detectable how they're doing it.

Keywords {๐Ÿ”}

pubmed, google, scholar, article, cas, gut, central, microbial, metabolites, microbiota, disease, butyrate, acid, effects, levels, studies, dietary, fatty, human, intestinal, cancer, mice, tmao, cell, scfas, acids, production, cells, sulfate, bacteria, host, metabolic, indole, receptor, inflammation, potential, obesity, bacterial, inhibition, res, function, conjugated, activation, health, linoleic, metabolite, formation, colorectal, colonic, sci,

Topics {โœ’๏ธ}

include myosin-cross-reactive antigen cyclooxygenase-related linoleate 10s-dioxygenase short-chain fatty acids nuclear magnetic resonance protein-bound uremic toxins gastric inhibitory polypeptide butyrate-dependent tumor-suppressive effect short-chain dehydrogenase/oxidoreductase high-fat diet-induced obesity microbiota-host metabolic interactions quantifying diet-induced metabolic g-protein-coupled receptor 43 g-protein-coupled receptor ischemia-induced neuronal damage conjugate linolenic acids nf-ฮบb pathway improved antioxidant/detoxifying defences udp-glucuronosyltransferase enzyme activities antibiotic-induced gut dysbiosis gpr40โ€“mekโ€“erk pathway [176] gpr40-mek-erk pathway increases th17-cell activity butyrate-mediated histone acetylation 10-hydroxy-cis-12-octadecenoic acid diet-dependent metabolic pathways metabolite-sensing receptor gpr43 satiety factor n-acylphosphatidylethanolamine article download pdf inoculating germ-free mice germ-free mice demonstrates intriguing diet-dependent metabolites high-fiber cereal supplement apolipoprotein e-deficient mice ppar-ฮณ-dependent mechanism metabolite-sensing receptors gpr43 epithelial barrier function host metabotype-microbiome associations metabolic profiling reveals choline trimethylamine-lyase expands gastric bypass surgery tang wh unusual rieske-type oxygenase lactic acid bacteria gut microbiota-brain communication protein-coupled receptors gpr41 host-microbial meta-metabolome o'keefe jh left-sided ulcerative colitis tight junction proteins complex cross-feeding

Questions {โ“}

  • Does butyrate protect from colorectal cancer?

Schema {๐Ÿ—บ๏ธ}

WebPage:
      mainEntity:
         headline:Microbial metabolism of dietary components to bioactive metabolites: opportunities for new therapeutic interventions
         description:Mass spectrometry- and nuclear magnetic resonance-based metabolomic studies comparing diseased versus healthy individuals have shown that microbial metabolites are often the compounds most markedly altered in the disease state. Recent studies suggest that several of these metabolites that derive from microbial transformation of dietary components have significant effects on physiological processes such as gut and immune homeostasis, energy metabolism, vascular function, and neurological behavior. Here, we review several of the most intriguing diet-dependent metabolites that may impact host physiology and may therefore be appropriate targets for therapeutic interventions, such as short-chain fatty acids, trimethylamine N-oxide, tryptophan and tyrosine derivatives, and oxidized fatty acids. Such interventions will require modulating either bacterial species or the bacterial biosynthetic enzymes required to produce these metabolites, so we briefly describe the current understanding of the bacterial and enzymatic pathways involved in their biosynthesis and summarize their molecular mechanisms of action. We then discuss in more detail the impact of these metabolites on health and disease, and review current strategies to modulate levels of these metabolites to promote human health. We also suggest future studies that are needed to realize the full therapeutic potential of targeting the gut microbiota.
         datePublished:2016-04-21T00:00:00Z
         dateModified:2016-04-21T00:00:00Z
         pageStart:1
         pageEnd:18
         license:http://creativecommons.org/publicdomain/zero/1.0/
         sameAs:https://doi.org/10.1186/s13073-016-0296-x
         keywords:
            Chronic Kidney Disease
            Conjugate Linoleic Acid
            HDAC Inhibition
            Gastric Inhibitory Polypeptide
            Microbial Metabolite
            Human Genetics
            Metabolomics
            Bioinformatics
            Medicine/Public Health
            general
            Cancer Research
            Systems Biology
         image:
            https://media.springernature.com/lw1200/springer-static/image/art%3A10.1186%2Fs13073-016-0296-x/MediaObjects/13073_2016_296_Fig1_HTML.gif
         isPartOf:
            name:Genome Medicine
            issn:
               1756-994X
            volumeNumber:8
            type:
               Periodical
               PublicationVolume
         publisher:
            name:BioMed Central
            logo:
               url:https://www.springernature.com/app-sn/public/images/logo-springernature.png
               type:ImageObject
            type:Organization
         author:
               name:Linda S. Zhang
               affiliation:
                     name:Vanderbilt University
                     address:
                        name:Division of Clinical Pharmacology, Vanderbilt University, Nashville, USA
                        type:PostalAddress
                     type:Organization
               type:Person
               name:Sean S. Davies
               affiliation:
                     name:Vanderbilt University
                     address:
                        name:Division of Clinical Pharmacology, Vanderbilt University, Nashville, USA
                        type:PostalAddress
                     type:Organization
                     name:Vanderbilt University
                     address:
                        name:Department of Pharmacology, Vanderbilt University, Nashville, USA
                        type:PostalAddress
                     type:Organization
                     name:Vanderbilt University
                     address:
                        name:Vanderbilt Institute of Chemical Biology, Vanderbilt University, Nashville, USA
                        type:PostalAddress
                     type:Organization
               email:[email protected]
               type:Person
         isAccessibleForFree:1
         type:ScholarlyArticle
      context:https://schema.org
ScholarlyArticle:
      headline:Microbial metabolism of dietary components to bioactive metabolites: opportunities for new therapeutic interventions
      description:Mass spectrometry- and nuclear magnetic resonance-based metabolomic studies comparing diseased versus healthy individuals have shown that microbial metabolites are often the compounds most markedly altered in the disease state. Recent studies suggest that several of these metabolites that derive from microbial transformation of dietary components have significant effects on physiological processes such as gut and immune homeostasis, energy metabolism, vascular function, and neurological behavior. Here, we review several of the most intriguing diet-dependent metabolites that may impact host physiology and may therefore be appropriate targets for therapeutic interventions, such as short-chain fatty acids, trimethylamine N-oxide, tryptophan and tyrosine derivatives, and oxidized fatty acids. Such interventions will require modulating either bacterial species or the bacterial biosynthetic enzymes required to produce these metabolites, so we briefly describe the current understanding of the bacterial and enzymatic pathways involved in their biosynthesis and summarize their molecular mechanisms of action. We then discuss in more detail the impact of these metabolites on health and disease, and review current strategies to modulate levels of these metabolites to promote human health. We also suggest future studies that are needed to realize the full therapeutic potential of targeting the gut microbiota.
      datePublished:2016-04-21T00:00:00Z
      dateModified:2016-04-21T00:00:00Z
      pageStart:1
      pageEnd:18
      license:http://creativecommons.org/publicdomain/zero/1.0/
      sameAs:https://doi.org/10.1186/s13073-016-0296-x
      keywords:
         Chronic Kidney Disease
         Conjugate Linoleic Acid
         HDAC Inhibition
         Gastric Inhibitory Polypeptide
         Microbial Metabolite
         Human Genetics
         Metabolomics
         Bioinformatics
         Medicine/Public Health
         general
         Cancer Research
         Systems Biology
      image:
         https://media.springernature.com/lw1200/springer-static/image/art%3A10.1186%2Fs13073-016-0296-x/MediaObjects/13073_2016_296_Fig1_HTML.gif
      isPartOf:
         name:Genome Medicine
         issn:
            1756-994X
         volumeNumber:8
         type:
            Periodical
            PublicationVolume
      publisher:
         name:BioMed Central
         logo:
            url:https://www.springernature.com/app-sn/public/images/logo-springernature.png
            type:ImageObject
         type:Organization
      author:
            name:Linda S. Zhang
            affiliation:
                  name:Vanderbilt University
                  address:
                     name:Division of Clinical Pharmacology, Vanderbilt University, Nashville, USA
                     type:PostalAddress
                  type:Organization
            type:Person
            name:Sean S. Davies
            affiliation:
                  name:Vanderbilt University
                  address:
                     name:Division of Clinical Pharmacology, Vanderbilt University, Nashville, USA
                     type:PostalAddress
                  type:Organization
                  name:Vanderbilt University
                  address:
                     name:Department of Pharmacology, Vanderbilt University, Nashville, USA
                     type:PostalAddress
                  type:Organization
                  name:Vanderbilt University
                  address:
                     name:Vanderbilt Institute of Chemical Biology, Vanderbilt University, Nashville, USA
                     type:PostalAddress
                  type:Organization
            email:[email protected]
            type:Person
      isAccessibleForFree:1
["Periodical","PublicationVolume"]:
      name:Genome Medicine
      issn:
         1756-994X
      volumeNumber:8
Organization:
      name:BioMed Central
      logo:
         url:https://www.springernature.com/app-sn/public/images/logo-springernature.png
         type:ImageObject
      name:Vanderbilt University
      address:
         name:Division of Clinical Pharmacology, Vanderbilt University, Nashville, USA
         type:PostalAddress
      name:Vanderbilt University
      address:
         name:Division of Clinical Pharmacology, Vanderbilt University, Nashville, USA
         type:PostalAddress
      name:Vanderbilt University
      address:
         name:Department of Pharmacology, Vanderbilt University, Nashville, USA
         type:PostalAddress
      name:Vanderbilt University
      address:
         name:Vanderbilt Institute of Chemical Biology, Vanderbilt University, Nashville, USA
         type:PostalAddress
ImageObject:
      url:https://www.springernature.com/app-sn/public/images/logo-springernature.png
Person:
      name:Linda S. Zhang
      affiliation:
            name:Vanderbilt University
            address:
               name:Division of Clinical Pharmacology, Vanderbilt University, Nashville, USA
               type:PostalAddress
            type:Organization
      name:Sean S. Davies
      affiliation:
            name:Vanderbilt University
            address:
               name:Division of Clinical Pharmacology, Vanderbilt University, Nashville, USA
               type:PostalAddress
            type:Organization
            name:Vanderbilt University
            address:
               name:Department of Pharmacology, Vanderbilt University, Nashville, USA
               type:PostalAddress
            type:Organization
            name:Vanderbilt University
            address:
               name:Vanderbilt Institute of Chemical Biology, Vanderbilt University, Nashville, USA
               type:PostalAddress
            type:Organization
      email:[email protected]
PostalAddress:
      name:Division of Clinical Pharmacology, Vanderbilt University, Nashville, USA
      name:Division of Clinical Pharmacology, Vanderbilt University, Nashville, USA
      name:Department of Pharmacology, Vanderbilt University, Nashville, USA
      name:Vanderbilt Institute of Chemical Biology, Vanderbilt University, Nashville, USA

External Links {๐Ÿ”—}(737)

Analytics and Tracking {๐Ÿ“Š}

  • Google Tag Manager

Libraries {๐Ÿ“š}

  • Clipboard.js
  • Prism.js

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  • Crossref

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