Effects of combined d-fagomine and omega-3 PUFAs on gut microbiota subpopulations and diabetes risk factors in rats fed a high-fat diet
Food contains bioactive compounds that may prevent changes in gut microbiota associated with Westernized diets. The aim of this study is to explore the possible additive effects of d -fagomine and ω-3 PUFAs (EPA/DHA 1:1) on gut microbiota and related risk factors during early stages in the developme...
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creator | Hereu, Mercè Ramos-Romero, Sara Busquets, Cristina Atienza, Lidia Amézqueta, Susana Miralles-Pérez, Bernat Nogués, Maria Rosa Méndez, Lucía Medina, Isabel Torres, Josep Lluís |
description | Food contains bioactive compounds that may prevent changes in gut microbiota associated with Westernized diets. The aim of this study is to explore the possible additive effects of
d
-fagomine and ω-3 PUFAs (EPA/DHA 1:1) on gut microbiota and related risk factors during early stages in the development of fat-induced pre-diabetes. Male Sprague Dawley (SD) rats were fed a standard diet, or a high-fat (HF) diet supplemented with
d
-fagomine, EPA/DHA 1:1, a combination of both, or neither, for 24 weeks. The variables measured were fasting glucose and glucose tolerance, plasma insulin, liver inflammation, fecal/cecal gut bacterial subgroups and short-chain fatty acids (SCFAs). The animals supplemented with
d
-fagomine alone and in combination with ω-3 PUFAs accumulated less fat than those in the non-supplemented HF group and those given only ω-3 PUFAs. The combined supplements attenuated the high-fat-induced incipient insulin resistance (IR), and liver inflammation, while increasing the cecal content, the Bacteroidetes:Firmicutes ratio and the populations of Bifidobacteriales. The functional effects of the combination of
d
-fagomine and EPA/DHA 1:1 against gut dysbiosis and the very early metabolic alterations induced by a high-fat diet are mainly those of
d
-fagomine complemented by the anti-inflammatory action of ω-3 PUFAs. |
doi_str_mv | 10.1038/s41598-019-52678-5 |
format | Article |
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d
-fagomine and ω-3 PUFAs (EPA/DHA 1:1) on gut microbiota and related risk factors during early stages in the development of fat-induced pre-diabetes. Male Sprague Dawley (SD) rats were fed a standard diet, or a high-fat (HF) diet supplemented with
d
-fagomine, EPA/DHA 1:1, a combination of both, or neither, for 24 weeks. The variables measured were fasting glucose and glucose tolerance, plasma insulin, liver inflammation, fecal/cecal gut bacterial subgroups and short-chain fatty acids (SCFAs). The animals supplemented with
d
-fagomine alone and in combination with ω-3 PUFAs accumulated less fat than those in the non-supplemented HF group and those given only ω-3 PUFAs. The combined supplements attenuated the high-fat-induced incipient insulin resistance (IR), and liver inflammation, while increasing the cecal content, the Bacteroidetes:Firmicutes ratio and the populations of Bifidobacteriales. The functional effects of the combination of
d
-fagomine and EPA/DHA 1:1 against gut dysbiosis and the very early metabolic alterations induced by a high-fat diet are mainly those of
d
-fagomine complemented by the anti-inflammatory action of ω-3 PUFAs.</description><identifier>ISSN: 2045-2322</identifier><identifier>EISSN: 2045-2322</identifier><identifier>DOI: 10.1038/s41598-019-52678-5</identifier><identifier>PMID: 31719544</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>14/63 ; 45/22 ; 45/77 ; 631/443/319/1642/2815 ; 692/700/2814 ; Animals ; Bioactive compounds ; Blood Glucose - analysis ; Cecum ; Developmental stages ; Diabetes ; Diabetes mellitus ; Diet ; Diet, High-Fat - adverse effects ; Dietary supplements ; Drug Therapy, Combination ; Dysbacteriosis ; Fatty acids ; Fatty Acids, Omega-3 - administration & dosage ; Fatty Acids, Omega-3 - therapeutic use ; Fish oils ; Gastrointestinal Microbiome - drug effects ; Glucose tolerance ; Glucose Tolerance Test ; Health risks ; High fat diet ; Humanities and Social Sciences ; Imino Pyranoses - administration & dosage ; Imino Pyranoses - therapeutic use ; Inflammation ; Insulin ; Insulin - blood ; Intestinal microflora ; Leptin - blood ; Liver ; Male ; Microbiota ; multidisciplinary ; Polyunsaturated fatty acids ; Prediabetic State - etiology ; Prediabetic State - microbiology ; Prediabetic State - prevention & control ; Rats ; Rats, Sprague-Dawley ; Risk Factors ; Science ; Science (multidisciplinary) ; Subpopulations</subject><ispartof>Scientific reports, 2019-11, Vol.9 (1), p.16628-12, Article 16628</ispartof><rights>The Author(s) 2019</rights><rights>2019. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c474t-c54b4df0c7b9bdb2a64ec277f1fc7aba2354e8b8b417cb7e599472d333acbf6f3</citedby><cites>FETCH-LOGICAL-c474t-c54b4df0c7b9bdb2a64ec277f1fc7aba2354e8b8b417cb7e599472d333acbf6f3</cites><orcidid>0000-0002-7349-8802</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6851385/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6851385/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,864,885,27923,27924,41119,42188,51575,53790,53792</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31719544$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hereu, Mercè</creatorcontrib><creatorcontrib>Ramos-Romero, Sara</creatorcontrib><creatorcontrib>Busquets, Cristina</creatorcontrib><creatorcontrib>Atienza, Lidia</creatorcontrib><creatorcontrib>Amézqueta, Susana</creatorcontrib><creatorcontrib>Miralles-Pérez, Bernat</creatorcontrib><creatorcontrib>Nogués, Maria Rosa</creatorcontrib><creatorcontrib>Méndez, Lucía</creatorcontrib><creatorcontrib>Medina, Isabel</creatorcontrib><creatorcontrib>Torres, Josep Lluís</creatorcontrib><title>Effects of combined d-fagomine and omega-3 PUFAs on gut microbiota subpopulations and diabetes risk factors in rats fed a high-fat diet</title><title>Scientific reports</title><addtitle>Sci Rep</addtitle><addtitle>Sci Rep</addtitle><description>Food contains bioactive compounds that may prevent changes in gut microbiota associated with Westernized diets. The aim of this study is to explore the possible additive effects of
d
-fagomine and ω-3 PUFAs (EPA/DHA 1:1) on gut microbiota and related risk factors during early stages in the development of fat-induced pre-diabetes. Male Sprague Dawley (SD) rats were fed a standard diet, or a high-fat (HF) diet supplemented with
d
-fagomine, EPA/DHA 1:1, a combination of both, or neither, for 24 weeks. The variables measured were fasting glucose and glucose tolerance, plasma insulin, liver inflammation, fecal/cecal gut bacterial subgroups and short-chain fatty acids (SCFAs). The animals supplemented with
d
-fagomine alone and in combination with ω-3 PUFAs accumulated less fat than those in the non-supplemented HF group and those given only ω-3 PUFAs. The combined supplements attenuated the high-fat-induced incipient insulin resistance (IR), and liver inflammation, while increasing the cecal content, the Bacteroidetes:Firmicutes ratio and the populations of Bifidobacteriales. The functional effects of the combination of
d
-fagomine and EPA/DHA 1:1 against gut dysbiosis and the very early metabolic alterations induced by a high-fat diet are mainly those of
d
-fagomine complemented by the anti-inflammatory action of ω-3 PUFAs.</description><subject>14/63</subject><subject>45/22</subject><subject>45/77</subject><subject>631/443/319/1642/2815</subject><subject>692/700/2814</subject><subject>Animals</subject><subject>Bioactive compounds</subject><subject>Blood Glucose - analysis</subject><subject>Cecum</subject><subject>Developmental stages</subject><subject>Diabetes</subject><subject>Diabetes mellitus</subject><subject>Diet</subject><subject>Diet, High-Fat - adverse effects</subject><subject>Dietary supplements</subject><subject>Drug Therapy, Combination</subject><subject>Dysbacteriosis</subject><subject>Fatty acids</subject><subject>Fatty Acids, Omega-3 - administration & dosage</subject><subject>Fatty Acids, Omega-3 - therapeutic use</subject><subject>Fish oils</subject><subject>Gastrointestinal Microbiome - drug effects</subject><subject>Glucose tolerance</subject><subject>Glucose Tolerance Test</subject><subject>Health risks</subject><subject>High fat diet</subject><subject>Humanities and Social Sciences</subject><subject>Imino Pyranoses - administration & dosage</subject><subject>Imino Pyranoses - therapeutic use</subject><subject>Inflammation</subject><subject>Insulin</subject><subject>Insulin - blood</subject><subject>Intestinal microflora</subject><subject>Leptin - blood</subject><subject>Liver</subject><subject>Male</subject><subject>Microbiota</subject><subject>multidisciplinary</subject><subject>Polyunsaturated fatty acids</subject><subject>Prediabetic State - etiology</subject><subject>Prediabetic State - microbiology</subject><subject>Prediabetic State - prevention & control</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Risk Factors</subject><subject>Science</subject><subject>Science (multidisciplinary)</subject><subject>Subpopulations</subject><issn>2045-2322</issn><issn>2045-2322</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>C6C</sourceid><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNp9kc9uFSEUxonR2Kb2BVwYEjdu0OHfZWZj0jStmjTRhV2TAwNzqTNwBaaJT-Bry-2ttbqQDSTnd77vHD6EXtLuLe14_64IKoeedHQgkm1UT-QTdMw6IQnjjD199D5Cp6XcdO1INgg6PEdHnCo6SCGO0c8L752tBSePbVpMiG7EI_EwpaW9McQRp8VNQDj-cn151sCIp7XiJdicTEgVcFnNLu3WGWpIsdy1jAGMq67gHMo37MHWlAsOEWdoXr55AN6GaduMaoNdfYGeeZiLO72_T9D15cXX84_k6vOHT-dnV8QKJSqxUhgx-s4qM5jRMNgIZ5lSnnqrwADjUrje9EZQZY1ychiEYiPnHKzxG89P0PuD7m41ixutizXDrHc5LJB_6ARB_12JYaundKs3vaS8l03gzb1ATt9XV6peQrFuniG6tBbNOBVMUiZUQ1__g96kNce23p7igxJSsUaxA9X-s5Ts_MMwtNP7qPUhat2i1ndR6_0Urx6v8dDyO9gG8ANQWilOLv_x_o_sL2r2tmc</recordid><startdate>20191112</startdate><enddate>20191112</enddate><creator>Hereu, Mercè</creator><creator>Ramos-Romero, Sara</creator><creator>Busquets, Cristina</creator><creator>Atienza, Lidia</creator><creator>Amézqueta, Susana</creator><creator>Miralles-Pérez, Bernat</creator><creator>Nogués, Maria Rosa</creator><creator>Méndez, Lucía</creator><creator>Medina, Isabel</creator><creator>Torres, Josep Lluís</creator><general>Nature Publishing Group UK</general><general>Nature Publishing Group</general><scope>C6C</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>88I</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-7349-8802</orcidid></search><sort><creationdate>20191112</creationdate><title>Effects of combined d-fagomine and omega-3 PUFAs on gut microbiota subpopulations and diabetes risk factors in rats fed a high-fat diet</title><author>Hereu, Mercè ; Ramos-Romero, Sara ; Busquets, Cristina ; Atienza, Lidia ; Amézqueta, Susana ; Miralles-Pérez, Bernat ; Nogués, Maria Rosa ; Méndez, Lucía ; Medina, Isabel ; Torres, Josep Lluís</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c474t-c54b4df0c7b9bdb2a64ec277f1fc7aba2354e8b8b417cb7e599472d333acbf6f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>14/63</topic><topic>45/22</topic><topic>45/77</topic><topic>631/443/319/1642/2815</topic><topic>692/700/2814</topic><topic>Animals</topic><topic>Bioactive compounds</topic><topic>Blood Glucose - analysis</topic><topic>Cecum</topic><topic>Developmental stages</topic><topic>Diabetes</topic><topic>Diabetes mellitus</topic><topic>Diet</topic><topic>Diet, High-Fat - adverse effects</topic><topic>Dietary supplements</topic><topic>Drug Therapy, Combination</topic><topic>Dysbacteriosis</topic><topic>Fatty acids</topic><topic>Fatty Acids, Omega-3 - administration & dosage</topic><topic>Fatty Acids, Omega-3 - therapeutic use</topic><topic>Fish oils</topic><topic>Gastrointestinal Microbiome - drug effects</topic><topic>Glucose tolerance</topic><topic>Glucose Tolerance Test</topic><topic>Health risks</topic><topic>High fat diet</topic><topic>Humanities and Social Sciences</topic><topic>Imino Pyranoses - administration & dosage</topic><topic>Imino Pyranoses - therapeutic use</topic><topic>Inflammation</topic><topic>Insulin</topic><topic>Insulin - blood</topic><topic>Intestinal microflora</topic><topic>Leptin - blood</topic><topic>Liver</topic><topic>Male</topic><topic>Microbiota</topic><topic>multidisciplinary</topic><topic>Polyunsaturated fatty acids</topic><topic>Prediabetic State - 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Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Scientific reports</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hereu, Mercè</au><au>Ramos-Romero, Sara</au><au>Busquets, Cristina</au><au>Atienza, Lidia</au><au>Amézqueta, Susana</au><au>Miralles-Pérez, Bernat</au><au>Nogués, Maria Rosa</au><au>Méndez, Lucía</au><au>Medina, Isabel</au><au>Torres, Josep Lluís</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effects of combined d-fagomine and omega-3 PUFAs on gut microbiota subpopulations and diabetes risk factors in rats fed a high-fat diet</atitle><jtitle>Scientific reports</jtitle><stitle>Sci Rep</stitle><addtitle>Sci Rep</addtitle><date>2019-11-12</date><risdate>2019</risdate><volume>9</volume><issue>1</issue><spage>16628</spage><epage>12</epage><pages>16628-12</pages><artnum>16628</artnum><issn>2045-2322</issn><eissn>2045-2322</eissn><abstract>Food contains bioactive compounds that may prevent changes in gut microbiota associated with Westernized diets. The aim of this study is to explore the possible additive effects of
d
-fagomine and ω-3 PUFAs (EPA/DHA 1:1) on gut microbiota and related risk factors during early stages in the development of fat-induced pre-diabetes. Male Sprague Dawley (SD) rats were fed a standard diet, or a high-fat (HF) diet supplemented with
d
-fagomine, EPA/DHA 1:1, a combination of both, or neither, for 24 weeks. The variables measured were fasting glucose and glucose tolerance, plasma insulin, liver inflammation, fecal/cecal gut bacterial subgroups and short-chain fatty acids (SCFAs). The animals supplemented with
d
-fagomine alone and in combination with ω-3 PUFAs accumulated less fat than those in the non-supplemented HF group and those given only ω-3 PUFAs. The combined supplements attenuated the high-fat-induced incipient insulin resistance (IR), and liver inflammation, while increasing the cecal content, the Bacteroidetes:Firmicutes ratio and the populations of Bifidobacteriales. The functional effects of the combination of
d
-fagomine and EPA/DHA 1:1 against gut dysbiosis and the very early metabolic alterations induced by a high-fat diet are mainly those of
d
-fagomine complemented by the anti-inflammatory action of ω-3 PUFAs.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>31719544</pmid><doi>10.1038/s41598-019-52678-5</doi><tpages>12</tpages><orcidid>https://orcid.org/0000-0002-7349-8802</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | 14/63 45/22 45/77 631/443/319/1642/2815 692/700/2814 Animals Bioactive compounds Blood Glucose - analysis Cecum Developmental stages Diabetes Diabetes mellitus Diet Diet, High-Fat - adverse effects Dietary supplements Drug Therapy, Combination Dysbacteriosis Fatty acids Fatty Acids, Omega-3 - administration & dosage Fatty Acids, Omega-3 - therapeutic use Fish oils Gastrointestinal Microbiome - drug effects Glucose tolerance Glucose Tolerance Test Health risks High fat diet Humanities and Social Sciences Imino Pyranoses - administration & dosage Imino Pyranoses - therapeutic use Inflammation Insulin Insulin - blood Intestinal microflora Leptin - blood Liver Male Microbiota multidisciplinary Polyunsaturated fatty acids Prediabetic State - etiology Prediabetic State - microbiology Prediabetic State - prevention & control Rats Rats, Sprague-Dawley Risk Factors Science Science (multidisciplinary) Subpopulations |
title | Effects of combined d-fagomine and omega-3 PUFAs on gut microbiota subpopulations and diabetes risk factors in rats fed a high-fat diet |
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