Academic Journal

Bioavailable Microbial Metabolites of Flavanols Demonstrate Highly Individualized Bioactivity on In Vitro β-Cell Functions Critical for Metabolic Health

التفاصيل البيبلوغرافية
العنوان: Bioavailable Microbial Metabolites of Flavanols Demonstrate Highly Individualized Bioactivity on In Vitro β-Cell Functions Critical for Metabolic Health
المؤلفون: Emily S. Krueger, Laura E. Griffin, Joseph L. Beales, Trevor S. Lloyd, Nathan J. Brown, Weston S. Elison, Colin D. Kay, Andrew P. Neilson, Jeffery S. Tessem
المصدر: Metabolites; Volume 13; Issue 7; Pages: 801
بيانات النشر: Multidisciplinary Digital Publishing Institute
سنة النشر: 2023
المجموعة: MDPI Open Access Publishing
مصطلحات موضوعية: gut microbiome, phytochemicals, flavanol metabolites, glucose sensitivity, responder analysis, personalized nutrition
الوصف: Dietary flavanols are known for disease preventative properties but are often poorly absorbed. Gut microbiome flavanol metabolites are more bioavailable and may exert protective activities. Using metabolite mixtures extracted from the urine of rats supplemented with flavanols and treated with or without antibiotics, we investigated their effects on INS-1 832/13 β-cell glucose stimulated insulin secretion (GSIS) capacity. We measured insulin secretion under non-stimulatory (low) and stimulatory (high) glucose levels, insulin secretion fold induction, and total insulin content. We conducted treatment-level comparisons, individual-level dose responses, and a responder vs. non-responder predictive analysis of metabolite composition. While the first two analyses did not elucidate treatment effects, metabolites from 9 of the 28 animals demonstrated significant dose responses, regardless of treatment. Differentiation of responders vs. non-responder revealed that levels of native flavanols and valerolactones approached significance for predicting enhanced GSIS, regardless of treatment. Although treatment-level patterns were not discernable, we conclude that the high inter-individual variability shows that metabolite bioactivity on GSIS capacity is less related to flavanol supplementation or antibiotic treatment and may be more associated with the unique microbiome or metabolome of each animal. These findings suggest flavanol metabolite activities are individualized and point to the need for personalized nutrition practices.
نوع الوثيقة: text
وصف الملف: application/pdf
اللغة: English
Relation: Nutrition and Metabolism; https://dx.doi.org/10.3390/metabo13070801
DOI: 10.3390/metabo13070801
الاتاحة: https://doi.org/10.3390/metabo13070801
Rights: https://creativecommons.org/licenses/by/4.0/
رقم الانضمام: edsbas.2DBECCD8
قاعدة البيانات: BASE
ResultId 1
Header edsbas
BASE
edsbas.2DBECCD8
961
3
Academic Journal
academicJournal
960.976379394531
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&scope=site&db=edsbas&AN=edsbas.2DBECCD8&custid=s6537998&authtype=sso
FullText Array ( [Availability] => 0 )
Array ( [0] => Array ( [Url] => https://doi.org/10.3390/metabo13070801# [Name] => EDS - BASE [Category] => fullText [Text] => View record in BASE [MouseOverText] => View record in BASE ) )
Items Array ( [Name] => Title [Label] => Title [Group] => Ti [Data] => Bioavailable Microbial Metabolites of Flavanols Demonstrate Highly Individualized Bioactivity on In Vitro β-Cell Functions Critical for Metabolic Health )
Array ( [Name] => Author [Label] => Authors [Group] => Au [Data] => <searchLink fieldCode="AR" term="%22Emily+S%2E+Krueger%22">Emily S. Krueger</searchLink><br /><searchLink fieldCode="AR" term="%22Laura+E%2E+Griffin%22">Laura E. Griffin</searchLink><br /><searchLink fieldCode="AR" term="%22Joseph+L%2E+Beales%22">Joseph L. Beales</searchLink><br /><searchLink fieldCode="AR" term="%22Trevor+S%2E+Lloyd%22">Trevor S. Lloyd</searchLink><br /><searchLink fieldCode="AR" term="%22Nathan+J%2E+Brown%22">Nathan J. Brown</searchLink><br /><searchLink fieldCode="AR" term="%22Weston+S%2E+Elison%22">Weston S. Elison</searchLink><br /><searchLink fieldCode="AR" term="%22Colin+D%2E+Kay%22">Colin D. Kay</searchLink><br /><searchLink fieldCode="AR" term="%22Andrew+P%2E+Neilson%22">Andrew P. Neilson</searchLink><br /><searchLink fieldCode="AR" term="%22Jeffery+S%2E+Tessem%22">Jeffery S. Tessem</searchLink> )
Array ( [Name] => TitleSource [Label] => Source [Group] => Src [Data] => Metabolites; Volume 13; Issue 7; Pages: 801 )
Array ( [Name] => Publisher [Label] => Publisher Information [Group] => PubInfo [Data] => Multidisciplinary Digital Publishing Institute )
Array ( [Name] => DatePubCY [Label] => Publication Year [Group] => Date [Data] => 2023 )
Array ( [Name] => Subset [Label] => Collection [Group] => HoldingsInfo [Data] => MDPI Open Access Publishing )
Array ( [Name] => Subject [Label] => Subject Terms [Group] => Su [Data] => <searchLink fieldCode="DE" term="%22gut+microbiome%22">gut microbiome</searchLink><br /><searchLink fieldCode="DE" term="%22phytochemicals%22">phytochemicals</searchLink><br /><searchLink fieldCode="DE" term="%22flavanol+metabolites%22">flavanol metabolites</searchLink><br /><searchLink fieldCode="DE" term="%22glucose+sensitivity%22">glucose sensitivity</searchLink><br /><searchLink fieldCode="DE" term="%22responder+analysis%22">responder analysis</searchLink><br /><searchLink fieldCode="DE" term="%22personalized+nutrition%22">personalized nutrition</searchLink> )
Array ( [Name] => Abstract [Label] => Description [Group] => Ab [Data] => Dietary flavanols are known for disease preventative properties but are often poorly absorbed. Gut microbiome flavanol metabolites are more bioavailable and may exert protective activities. Using metabolite mixtures extracted from the urine of rats supplemented with flavanols and treated with or without antibiotics, we investigated their effects on INS-1 832/13 β-cell glucose stimulated insulin secretion (GSIS) capacity. We measured insulin secretion under non-stimulatory (low) and stimulatory (high) glucose levels, insulin secretion fold induction, and total insulin content. We conducted treatment-level comparisons, individual-level dose responses, and a responder vs. non-responder predictive analysis of metabolite composition. While the first two analyses did not elucidate treatment effects, metabolites from 9 of the 28 animals demonstrated significant dose responses, regardless of treatment. Differentiation of responders vs. non-responder revealed that levels of native flavanols and valerolactones approached significance for predicting enhanced GSIS, regardless of treatment. Although treatment-level patterns were not discernable, we conclude that the high inter-individual variability shows that metabolite bioactivity on GSIS capacity is less related to flavanol supplementation or antibiotic treatment and may be more associated with the unique microbiome or metabolome of each animal. These findings suggest flavanol metabolite activities are individualized and point to the need for personalized nutrition practices. )
Array ( [Name] => TypeDocument [Label] => Document Type [Group] => TypDoc [Data] => text )
Array ( [Name] => Format [Label] => File Description [Group] => SrcInfo [Data] => application/pdf )
Array ( [Name] => Language [Label] => Language [Group] => Lang [Data] => English )
Array ( [Name] => NoteTitleSource [Label] => Relation [Group] => SrcInfo [Data] => Nutrition and Metabolism; https://dx.doi.org/10.3390/metabo13070801 )
Array ( [Name] => DOI [Label] => DOI [Group] => ID [Data] => 10.3390/metabo13070801 )
Array ( [Name] => URL [Label] => Availability [Group] => URL [Data] => https://doi.org/10.3390/metabo13070801 )
Array ( [Name] => Copyright [Label] => Rights [Group] => Cpyrght [Data] => https://creativecommons.org/licenses/by/4.0/ )
Array ( [Name] => AN [Label] => Accession Number [Group] => ID [Data] => edsbas.2DBECCD8 )
RecordInfo Array ( [BibEntity] => Array ( [Identifiers] => Array ( [0] => Array ( [Type] => doi [Value] => 10.3390/metabo13070801 ) ) [Languages] => Array ( [0] => Array ( [Text] => English ) ) [Subjects] => Array ( [0] => Array ( [SubjectFull] => gut microbiome [Type] => general ) [1] => Array ( [SubjectFull] => phytochemicals [Type] => general ) [2] => Array ( [SubjectFull] => flavanol metabolites [Type] => general ) [3] => Array ( [SubjectFull] => glucose sensitivity [Type] => general ) [4] => Array ( [SubjectFull] => responder analysis [Type] => general ) [5] => Array ( [SubjectFull] => personalized nutrition [Type] => general ) ) [Titles] => Array ( [0] => Array ( [TitleFull] => Bioavailable Microbial Metabolites of Flavanols Demonstrate Highly Individualized Bioactivity on In Vitro β-Cell Functions Critical for Metabolic Health [Type] => main ) ) ) [BibRelationships] => Array ( [HasContributorRelationships] => Array ( [0] => Array ( [PersonEntity] => Array ( [Name] => Array ( [NameFull] => Emily S. Krueger ) ) ) [1] => Array ( [PersonEntity] => Array ( [Name] => Array ( [NameFull] => Laura E. Griffin ) ) ) [2] => Array ( [PersonEntity] => Array ( [Name] => Array ( [NameFull] => Joseph L. Beales ) ) ) [3] => Array ( [PersonEntity] => Array ( [Name] => Array ( [NameFull] => Trevor S. Lloyd ) ) ) [4] => Array ( [PersonEntity] => Array ( [Name] => Array ( [NameFull] => Nathan J. Brown ) ) ) [5] => Array ( [PersonEntity] => Array ( [Name] => Array ( [NameFull] => Weston S. Elison ) ) ) [6] => Array ( [PersonEntity] => Array ( [Name] => Array ( [NameFull] => Colin D. Kay ) ) ) [7] => Array ( [PersonEntity] => Array ( [Name] => Array ( [NameFull] => Andrew P. Neilson ) ) ) [8] => Array ( [PersonEntity] => Array ( [Name] => Array ( [NameFull] => Jeffery S. Tessem ) ) ) ) [IsPartOfRelationships] => Array ( [0] => Array ( [BibEntity] => Array ( [Dates] => Array ( [0] => Array ( [D] => 01 [M] => 01 [Type] => published [Y] => 2023 ) ) [Identifiers] => Array ( [0] => Array ( [Type] => issn-locals [Value] => edsbas ) [1] => Array ( [Type] => issn-locals [Value] => edsbas.oa ) ) [Titles] => Array ( [0] => Array ( [TitleFull] => Metabolites; Volume 13; Issue 7; Pages: 801 [Type] => main ) ) ) ) ) ) )
IllustrationInfo