Chicory increases acetate turnover, but not propionate and butyrate peripheral turnovers in rats
Chicory roots are rich in inulin that is degraded into SCFA in the caecum and colon. Whole-body SCFA metabolism was investigated in rats during food deprivation and postprandial states. After 22 h of food deprivation, sixteen rats received an IV injection of radioactive 14C-labelled SCFA. The volume...
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Veröffentlicht in: | British journal of nutrition 2008-02, Vol.99 (2), p.287-296 |
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description | Chicory roots are rich in inulin that is degraded into SCFA in the caecum and colon. Whole-body SCFA metabolism was investigated in rats during food deprivation and postprandial states. After 22 h of food deprivation, sixteen rats received an IV injection of radioactive 14C-labelled SCFA. The volume of distribution and the fractional clearance rate of SCFA were 0·25–0·27 litres/kg and 5·4–5·9 %/min, respectively. The half-life in the first extracellular rapidly decaying compartment was between 0·9 and 1·4 min. After 22 h of food deprivation, another seventeen rats received a primed continuous IV infusion of 13C-labelled SCFA for 2 h. Isotope enrichment (13C) of SCFA was determined in peripheral arterial blood by MS. Peripheral acetate, propionate and butyrate turnover rates were 29, 4 and 0·3 μmol/kg per min respectively. Following 4 weeks of treatment with chicory root or control diets, eighteen fed rats received a primed continuous IV infusion of 13C-labelled SCFA for 2 h. Intestinal degradation of dietary chicory lowered caecal pH, enhanced caecal and colonic weights, caecal SCFA concentrations and breath H2.The diet with chicory supplementation enhanced peripheral acetate turnover by 25 % (P = 0·017) concomitant with an increase in plasma acetate concentration. There were no changes in propionate or butyrate turnovers. In conclusion, by setting up a multi-tracer approach to simultaneously assess the turnovers of acetate, propionate and butyrate it was demonstrated that a chronic chicory-rich diet significantly increases peripheral acetate turnover but not that of propionate or butyrate in rats. |
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Whole-body SCFA metabolism was investigated in rats during food deprivation and postprandial states. After 22 h of food deprivation, sixteen rats received an IV injection of radioactive 14C-labelled SCFA. The volume of distribution and the fractional clearance rate of SCFA were 0·25–0·27 litres/kg and 5·4–5·9 %/min, respectively. The half-life in the first extracellular rapidly decaying compartment was between 0·9 and 1·4 min. After 22 h of food deprivation, another seventeen rats received a primed continuous IV infusion of 13C-labelled SCFA for 2 h. Isotope enrichment (13C) of SCFA was determined in peripheral arterial blood by MS. Peripheral acetate, propionate and butyrate turnover rates were 29, 4 and 0·3 μmol/kg per min respectively. Following 4 weeks of treatment with chicory root or control diets, eighteen fed rats received a primed continuous IV infusion of 13C-labelled SCFA for 2 h. Intestinal degradation of dietary chicory lowered caecal pH, enhanced caecal and colonic weights, caecal SCFA concentrations and breath H2.The diet with chicory supplementation enhanced peripheral acetate turnover by 25 % (P = 0·017) concomitant with an increase in plasma acetate concentration. There were no changes in propionate or butyrate turnovers. In conclusion, by setting up a multi-tracer approach to simultaneously assess the turnovers of acetate, propionate and butyrate it was demonstrated that a chronic chicory-rich diet significantly increases peripheral acetate turnover but not that of propionate or butyrate in rats.</description><identifier>ISSN: 0007-1145</identifier><identifier>EISSN: 1475-2662</identifier><identifier>DOI: 10.1017/S0007114507815790</identifier><identifier>PMID: 17761014</identifier><language>eng</language><publisher>Cambridge, UK: Cambridge University Press</publisher><subject>Acetates - blood ; acetic acid ; animal models ; Animals ; blood chemistry ; blood lipids ; Butyrates - blood ; butyric acid ; Carbon Radioisotopes ; cecum ; Cecum - metabolism ; Chicory ; Cichorium intybus ; colon ; Colon - metabolism ; experimental design ; Fatty Acids, Volatile - biosynthesis ; Fatty Acids, Volatile - blood ; feed deprivation ; Female ; Food Deprivation - physiology ; Half-Life ; inulin ; isotope labeling ; Kinetics ; lipid metabolism ; Male ; Portal Vein - metabolism ; Postprandial Period - physiology ; prebiotics ; Propionates - blood ; propionic acid ; Rats ; Short-chain fatty acids ; tissue weight</subject><ispartof>British journal of nutrition, 2008-02, Vol.99 (2), p.287-296</ispartof><rights>Copyright © Nestec Ltd 2007</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c448t-28fe3d2d568ea1b0b34c1933d7dcf0c2612a03f61348a7c6aa49c377ca6f5083</citedby><cites>FETCH-LOGICAL-c448t-28fe3d2d568ea1b0b34c1933d7dcf0c2612a03f61348a7c6aa49c377ca6f5083</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.cambridge.org/core/product/identifier/S0007114507815790/type/journal_article$$EHTML$$P50$$Gcambridge$$H</linktohtml><link.rule.ids>164,314,776,780,27901,27902,55603</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17761014$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Pouteau, Etienne</creatorcontrib><creatorcontrib>Rochat, Florence</creatorcontrib><creatorcontrib>Jann, Alfred</creatorcontrib><creatorcontrib>Meirim, Isabelle</creatorcontrib><creatorcontrib>Sanchez-Garcia, Jose-Luis</creatorcontrib><creatorcontrib>Ornstein, Kurt</creatorcontrib><creatorcontrib>German, Bruce</creatorcontrib><creatorcontrib>Ballèvre, Olivier</creatorcontrib><title>Chicory increases acetate turnover, but not propionate and butyrate peripheral turnovers in rats</title><title>British journal of nutrition</title><addtitle>Br J Nutr</addtitle><description>Chicory roots are rich in inulin that is degraded into SCFA in the caecum and colon. Whole-body SCFA metabolism was investigated in rats during food deprivation and postprandial states. After 22 h of food deprivation, sixteen rats received an IV injection of radioactive 14C-labelled SCFA. The volume of distribution and the fractional clearance rate of SCFA were 0·25–0·27 litres/kg and 5·4–5·9 %/min, respectively. The half-life in the first extracellular rapidly decaying compartment was between 0·9 and 1·4 min. After 22 h of food deprivation, another seventeen rats received a primed continuous IV infusion of 13C-labelled SCFA for 2 h. Isotope enrichment (13C) of SCFA was determined in peripheral arterial blood by MS. Peripheral acetate, propionate and butyrate turnover rates were 29, 4 and 0·3 μmol/kg per min respectively. Following 4 weeks of treatment with chicory root or control diets, eighteen fed rats received a primed continuous IV infusion of 13C-labelled SCFA for 2 h. Intestinal degradation of dietary chicory lowered caecal pH, enhanced caecal and colonic weights, caecal SCFA concentrations and breath H2.The diet with chicory supplementation enhanced peripheral acetate turnover by 25 % (P = 0·017) concomitant with an increase in plasma acetate concentration. There were no changes in propionate or butyrate turnovers. In conclusion, by setting up a multi-tracer approach to simultaneously assess the turnovers of acetate, propionate and butyrate it was demonstrated that a chronic chicory-rich diet significantly increases peripheral acetate turnover but not that of propionate or butyrate in rats.</description><subject>Acetates - blood</subject><subject>acetic acid</subject><subject>animal models</subject><subject>Animals</subject><subject>blood chemistry</subject><subject>blood lipids</subject><subject>Butyrates - blood</subject><subject>butyric acid</subject><subject>Carbon Radioisotopes</subject><subject>cecum</subject><subject>Cecum - metabolism</subject><subject>Chicory</subject><subject>Cichorium intybus</subject><subject>colon</subject><subject>Colon - metabolism</subject><subject>experimental design</subject><subject>Fatty Acids, Volatile - biosynthesis</subject><subject>Fatty Acids, Volatile - blood</subject><subject>feed deprivation</subject><subject>Female</subject><subject>Food Deprivation - physiology</subject><subject>Half-Life</subject><subject>inulin</subject><subject>isotope labeling</subject><subject>Kinetics</subject><subject>lipid metabolism</subject><subject>Male</subject><subject>Portal Vein - metabolism</subject><subject>Postprandial Period - physiology</subject><subject>prebiotics</subject><subject>Propionates - blood</subject><subject>propionic acid</subject><subject>Rats</subject><subject>Short-chain fatty acids</subject><subject>tissue weight</subject><issn>0007-1145</issn><issn>1475-2662</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kUFP3DAQhS1UBAvlB_RScuqJUE_s2M4RbYFWTVW10LOZOA4YduNgJ1X339fRruBQqSdr_L55enpDyDug50BBfryhlEoAXlKpoJQV3SML4LLMCyGKN2Qxy_msH5KjGB_TqIBWB-QQpBTJgS_I3fLBGR82metNsBhtzNDYEUebjVPo_W8bzrJmGrPej9kQ_OB8P4vYt_P3JszDYIMbHmzA1ctSTIZZEuNbst_hKtqT3XtMbq8ub5ef8_r79ZflRZ0bztWYF6qzrC3aUiiL0NCGcQMVY61sTUdNIaBAyjoBjCuURiDyyjApDYqupIodkw9b25TxebJx1GsXjV2tsLd-ilpSqLgseAJhC5rgYwy200NwawwbDVTPrep_Wk0773fmU7O27evGrsYE5FvAxdH-edExPGkhmSy1uP6hf377CupTXes68adbvkOv8T64qH_dFBRYupCoFJOJYLuYuG6Ca--tfvSp21Thf4L-BU7jmvo</recordid><startdate>20080201</startdate><enddate>20080201</enddate><creator>Pouteau, Etienne</creator><creator>Rochat, Florence</creator><creator>Jann, Alfred</creator><creator>Meirim, Isabelle</creator><creator>Sanchez-Garcia, Jose-Luis</creator><creator>Ornstein, Kurt</creator><creator>German, Bruce</creator><creator>Ballèvre, Olivier</creator><general>Cambridge University Press</general><scope>FBQ</scope><scope>BSCLL</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>7X8</scope></search><sort><creationdate>20080201</creationdate><title>Chicory increases acetate turnover, but not propionate and butyrate peripheral turnovers in rats</title><author>Pouteau, Etienne ; Rochat, Florence ; Jann, Alfred ; Meirim, Isabelle ; Sanchez-Garcia, Jose-Luis ; Ornstein, Kurt ; German, Bruce ; Ballèvre, Olivier</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c448t-28fe3d2d568ea1b0b34c1933d7dcf0c2612a03f61348a7c6aa49c377ca6f5083</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Acetates - blood</topic><topic>acetic acid</topic><topic>animal models</topic><topic>Animals</topic><topic>blood chemistry</topic><topic>blood lipids</topic><topic>Butyrates - blood</topic><topic>butyric acid</topic><topic>Carbon Radioisotopes</topic><topic>cecum</topic><topic>Cecum - metabolism</topic><topic>Chicory</topic><topic>Cichorium intybus</topic><topic>colon</topic><topic>Colon - metabolism</topic><topic>experimental design</topic><topic>Fatty Acids, Volatile - biosynthesis</topic><topic>Fatty Acids, Volatile - blood</topic><topic>feed deprivation</topic><topic>Female</topic><topic>Food Deprivation - physiology</topic><topic>Half-Life</topic><topic>inulin</topic><topic>isotope labeling</topic><topic>Kinetics</topic><topic>lipid metabolism</topic><topic>Male</topic><topic>Portal Vein - metabolism</topic><topic>Postprandial Period - physiology</topic><topic>prebiotics</topic><topic>Propionates - blood</topic><topic>propionic acid</topic><topic>Rats</topic><topic>Short-chain fatty acids</topic><topic>tissue weight</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Pouteau, Etienne</creatorcontrib><creatorcontrib>Rochat, Florence</creatorcontrib><creatorcontrib>Jann, Alfred</creatorcontrib><creatorcontrib>Meirim, Isabelle</creatorcontrib><creatorcontrib>Sanchez-Garcia, Jose-Luis</creatorcontrib><creatorcontrib>Ornstein, Kurt</creatorcontrib><creatorcontrib>German, Bruce</creatorcontrib><creatorcontrib>Ballèvre, Olivier</creatorcontrib><collection>AGRIS</collection><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>British journal of nutrition</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Pouteau, Etienne</au><au>Rochat, Florence</au><au>Jann, Alfred</au><au>Meirim, Isabelle</au><au>Sanchez-Garcia, Jose-Luis</au><au>Ornstein, Kurt</au><au>German, Bruce</au><au>Ballèvre, Olivier</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Chicory increases acetate turnover, but not propionate and butyrate peripheral turnovers in rats</atitle><jtitle>British journal of nutrition</jtitle><addtitle>Br J Nutr</addtitle><date>2008-02-01</date><risdate>2008</risdate><volume>99</volume><issue>2</issue><spage>287</spage><epage>296</epage><pages>287-296</pages><issn>0007-1145</issn><eissn>1475-2662</eissn><abstract>Chicory roots are rich in inulin that is degraded into SCFA in the caecum and colon. Whole-body SCFA metabolism was investigated in rats during food deprivation and postprandial states. After 22 h of food deprivation, sixteen rats received an IV injection of radioactive 14C-labelled SCFA. The volume of distribution and the fractional clearance rate of SCFA were 0·25–0·27 litres/kg and 5·4–5·9 %/min, respectively. The half-life in the first extracellular rapidly decaying compartment was between 0·9 and 1·4 min. After 22 h of food deprivation, another seventeen rats received a primed continuous IV infusion of 13C-labelled SCFA for 2 h. Isotope enrichment (13C) of SCFA was determined in peripheral arterial blood by MS. Peripheral acetate, propionate and butyrate turnover rates were 29, 4 and 0·3 μmol/kg per min respectively. Following 4 weeks of treatment with chicory root or control diets, eighteen fed rats received a primed continuous IV infusion of 13C-labelled SCFA for 2 h. Intestinal degradation of dietary chicory lowered caecal pH, enhanced caecal and colonic weights, caecal SCFA concentrations and breath H2.The diet with chicory supplementation enhanced peripheral acetate turnover by 25 % (P = 0·017) concomitant with an increase in plasma acetate concentration. There were no changes in propionate or butyrate turnovers. In conclusion, by setting up a multi-tracer approach to simultaneously assess the turnovers of acetate, propionate and butyrate it was demonstrated that a chronic chicory-rich diet significantly increases peripheral acetate turnover but not that of propionate or butyrate in rats.</abstract><cop>Cambridge, UK</cop><pub>Cambridge University Press</pub><pmid>17761014</pmid><doi>10.1017/S0007114507815790</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Acetates - blood acetic acid animal models Animals blood chemistry blood lipids Butyrates - blood butyric acid Carbon Radioisotopes cecum Cecum - metabolism Chicory Cichorium intybus colon Colon - metabolism experimental design Fatty Acids, Volatile - biosynthesis Fatty Acids, Volatile - blood feed deprivation Female Food Deprivation - physiology Half-Life inulin isotope labeling Kinetics lipid metabolism Male Portal Vein - metabolism Postprandial Period - physiology prebiotics Propionates - blood propionic acid Rats Short-chain fatty acids tissue weight |
title | Chicory increases acetate turnover, but not propionate and butyrate peripheral turnovers in rats |
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