Metabolism of glycerol-1,2,3-trimethylsuccinate in rat hepatocytes
The metabolism of glycerol-1,2,3-trimethylsuccinate ester was investigated in rat hepatocytes. The ester displayed a greater nutritional value than D-glucose, as a precursor of either CO2 or glycogen. In terms of 14CO2 production, the value calculated from experiments conducted in the presence of 1....
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Veröffentlicht in: | Molecular and cellular biochemistry 1999-08, Vol.198 (1-2), p.135-139 |
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description | The metabolism of glycerol-1,2,3-trimethylsuccinate ester was investigated in rat hepatocytes. The ester displayed a greater nutritional value than D-glucose, as a precursor of either CO2 or glycogen. In terms of 14CO2 production, the value calculated from experiments conducted in the presence of 1.9 mM [U-14C] glycerol-1,2,3-trimethylsuccinate, glycerol-1,2,3-trimethyl[1,4-14C] succinate and glycerol- 1,2,3-trimethyl[2,3-14C] succinate represented about 50 times that found in cells incubated with 1.0 mM D-[U-14C] glucose. For glycogen synthesis, the results found with the ester were approximately 7-8 times higher than those found with the hexose. A further advantage of the ester over D-glucose consisted in the fact that, at increasing concentrations of these nutrients, a maximal metabolic response may be reached at lower levels of glycerol- 1,2,3-trimethylsuccinate than D-glucose. By comparison with previous data obtained in the same experimental model, glycerol-1,2,3-trimethylsuccinate was also found to display a higher nutritional value than the dimethyl ester of succinic acid. It is proposed, therefore, that glycerol-1,2,3-trimethylsuccinate could be used to support ATP generation in cells endangered by an imbalance between the rate of synthesis and hydrolysis of this adenine nucleotide. |
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The ester displayed a greater nutritional value than D-glucose, as a precursor of either CO2 or glycogen. In terms of 14CO2 production, the value calculated from experiments conducted in the presence of 1.9 mM [U-14C] glycerol-1,2,3-trimethylsuccinate, glycerol-1,2,3-trimethyl[1,4-14C] succinate and glycerol- 1,2,3-trimethyl[2,3-14C] succinate represented about 50 times that found in cells incubated with 1.0 mM D-[U-14C] glucose. For glycogen synthesis, the results found with the ester were approximately 7-8 times higher than those found with the hexose. A further advantage of the ester over D-glucose consisted in the fact that, at increasing concentrations of these nutrients, a maximal metabolic response may be reached at lower levels of glycerol- 1,2,3-trimethylsuccinate than D-glucose. By comparison with previous data obtained in the same experimental model, glycerol-1,2,3-trimethylsuccinate was also found to display a higher nutritional value than the dimethyl ester of succinic acid. It is proposed, therefore, that glycerol-1,2,3-trimethylsuccinate could be used to support ATP generation in cells endangered by an imbalance between the rate of synthesis and hydrolysis of this adenine nucleotide.</description><identifier>ISSN: 0300-8177</identifier><identifier>EISSN: 1573-4919</identifier><identifier>DOI: 10.1023/A:1006949914417</identifier><identifier>PMID: 10497888</identifier><language>eng</language><publisher>Netherlands: Springer Nature B.V</publisher><subject>Amino Acids - biosynthesis ; Animals ; Carbon Dioxide ; Carbon Radioisotopes ; Chloride Channels - metabolism ; Female ; Glucose - biosynthesis ; Glycerol - analogs & derivatives ; Glycogen - biosynthesis ; Hydrogen-Ion Concentration ; Liver - cytology ; Liver - metabolism ; Metabolism ; Nutritive value ; Rats ; Rats, Wistar ; Succinates</subject><ispartof>Molecular and cellular biochemistry, 1999-08, Vol.198 (1-2), p.135-139</ispartof><rights>Kluwer Academic Publishers 1999</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c312t-123ebe178ae3a63730f05c181024cd7a570803329089c8f2ddd7a916d8aec5253</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10497888$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ladrière, L</creatorcontrib><creatorcontrib>Grue-Sørensen, G</creatorcontrib><creatorcontrib>Björkling, F</creatorcontrib><creatorcontrib>Malaisse, W J</creatorcontrib><title>Metabolism of glycerol-1,2,3-trimethylsuccinate in rat hepatocytes</title><title>Molecular and cellular biochemistry</title><addtitle>Mol Cell Biochem</addtitle><description>The metabolism of glycerol-1,2,3-trimethylsuccinate ester was investigated in rat hepatocytes. The ester displayed a greater nutritional value than D-glucose, as a precursor of either CO2 or glycogen. In terms of 14CO2 production, the value calculated from experiments conducted in the presence of 1.9 mM [U-14C] glycerol-1,2,3-trimethylsuccinate, glycerol-1,2,3-trimethyl[1,4-14C] succinate and glycerol- 1,2,3-trimethyl[2,3-14C] succinate represented about 50 times that found in cells incubated with 1.0 mM D-[U-14C] glucose. For glycogen synthesis, the results found with the ester were approximately 7-8 times higher than those found with the hexose. A further advantage of the ester over D-glucose consisted in the fact that, at increasing concentrations of these nutrients, a maximal metabolic response may be reached at lower levels of glycerol- 1,2,3-trimethylsuccinate than D-glucose. By comparison with previous data obtained in the same experimental model, glycerol-1,2,3-trimethylsuccinate was also found to display a higher nutritional value than the dimethyl ester of succinic acid. It is proposed, therefore, that glycerol-1,2,3-trimethylsuccinate could be used to support ATP generation in cells endangered by an imbalance between the rate of synthesis and hydrolysis of this adenine nucleotide.</description><subject>Amino Acids - biosynthesis</subject><subject>Animals</subject><subject>Carbon Dioxide</subject><subject>Carbon Radioisotopes</subject><subject>Chloride Channels - metabolism</subject><subject>Female</subject><subject>Glucose - biosynthesis</subject><subject>Glycerol - analogs & derivatives</subject><subject>Glycogen - biosynthesis</subject><subject>Hydrogen-Ion Concentration</subject><subject>Liver - cytology</subject><subject>Liver - metabolism</subject><subject>Metabolism</subject><subject>Nutritive value</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>Succinates</subject><issn>0300-8177</issn><issn>1573-4919</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><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>eNp90DtPwzAQB3ALgWgpzGwoYoClgTs_YputVLykIhaYI9dxaKo8SuwM-fYYAQsD00mn393pf4ScIlwhUHa9uEGATHOtkXOUe2SKQrKUa9T7ZAoMIFUo5YQceb8FiBjxkEwQuJZKqSm5fXbBrLu68k3Slcl7PVrXd3WKczpnaeirxoXNWPvB2qo1wSVVm_QmJBu3M6GzY3D-mByUpvbu5KfOyNv93evyMV29PDwtF6vUMqQhRcrc2qFUxjGTMcmgBGFRxRzcFtIICQoYoxqUtqqkRRGbGrMiDlhBBZuRy--9u777GJwPeVN56-ratK4bfK5QCJYpKqO8-FdKAK6kohGe_4HbbujbmCKXIqMcRPZ19-wHDevGFfkuPsX0Y_77RPYJ0b5xDg</recordid><startdate>19990801</startdate><enddate>19990801</enddate><creator>Ladrière, L</creator><creator>Grue-Sørensen, G</creator><creator>Björkling, F</creator><creator>Malaisse, W J</creator><general>Springer Nature B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>3V.</scope><scope>7QL</scope><scope>7QP</scope><scope>7T5</scope><scope>7T7</scope><scope>7TK</scope><scope>7TM</scope><scope>7TO</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>88I</scope><scope>8AO</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7N</scope><scope>M7P</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>RC3</scope><scope>7X8</scope><scope>7U7</scope></search><sort><creationdate>19990801</creationdate><title>Metabolism of glycerol-1,2,3-trimethylsuccinate in rat hepatocytes</title><author>Ladrière, L ; Grue-Sørensen, G ; Björkling, F ; Malaisse, W J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c312t-123ebe178ae3a63730f05c181024cd7a570803329089c8f2ddd7a916d8aec5253</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1999</creationdate><topic>Amino Acids - biosynthesis</topic><topic>Animals</topic><topic>Carbon Dioxide</topic><topic>Carbon Radioisotopes</topic><topic>Chloride Channels - metabolism</topic><topic>Female</topic><topic>Glucose - biosynthesis</topic><topic>Glycerol - analogs & derivatives</topic><topic>Glycogen - biosynthesis</topic><topic>Hydrogen-Ion Concentration</topic><topic>Liver - cytology</topic><topic>Liver - metabolism</topic><topic>Metabolism</topic><topic>Nutritive value</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>Succinates</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ladrière, L</creatorcontrib><creatorcontrib>Grue-Sørensen, G</creatorcontrib><creatorcontrib>Björkling, F</creatorcontrib><creatorcontrib>Malaisse, W J</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>ProQuest Central (Corporate)</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Immunology Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Science Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biological Science Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central Basic</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>Toxicology Abstracts</collection><jtitle>Molecular and cellular biochemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ladrière, L</au><au>Grue-Sørensen, G</au><au>Björkling, F</au><au>Malaisse, W J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Metabolism of glycerol-1,2,3-trimethylsuccinate in rat hepatocytes</atitle><jtitle>Molecular and cellular biochemistry</jtitle><addtitle>Mol Cell Biochem</addtitle><date>1999-08-01</date><risdate>1999</risdate><volume>198</volume><issue>1-2</issue><spage>135</spage><epage>139</epage><pages>135-139</pages><issn>0300-8177</issn><eissn>1573-4919</eissn><abstract>The metabolism of glycerol-1,2,3-trimethylsuccinate ester was investigated in rat hepatocytes. The ester displayed a greater nutritional value than D-glucose, as a precursor of either CO2 or glycogen. In terms of 14CO2 production, the value calculated from experiments conducted in the presence of 1.9 mM [U-14C] glycerol-1,2,3-trimethylsuccinate, glycerol-1,2,3-trimethyl[1,4-14C] succinate and glycerol- 1,2,3-trimethyl[2,3-14C] succinate represented about 50 times that found in cells incubated with 1.0 mM D-[U-14C] glucose. For glycogen synthesis, the results found with the ester were approximately 7-8 times higher than those found with the hexose. A further advantage of the ester over D-glucose consisted in the fact that, at increasing concentrations of these nutrients, a maximal metabolic response may be reached at lower levels of glycerol- 1,2,3-trimethylsuccinate than D-glucose. By comparison with previous data obtained in the same experimental model, glycerol-1,2,3-trimethylsuccinate was also found to display a higher nutritional value than the dimethyl ester of succinic acid. It is proposed, therefore, that glycerol-1,2,3-trimethylsuccinate could be used to support ATP generation in cells endangered by an imbalance between the rate of synthesis and hydrolysis of this adenine nucleotide.</abstract><cop>Netherlands</cop><pub>Springer Nature B.V</pub><pmid>10497888</pmid><doi>10.1023/A:1006949914417</doi><tpages>5</tpages></addata></record> |
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subjects | Amino Acids - biosynthesis Animals Carbon Dioxide Carbon Radioisotopes Chloride Channels - metabolism Female Glucose - biosynthesis Glycerol - analogs & derivatives Glycogen - biosynthesis Hydrogen-Ion Concentration Liver - cytology Liver - metabolism Metabolism Nutritive value Rats Rats, Wistar Succinates |
title | Metabolism of glycerol-1,2,3-trimethylsuccinate in rat hepatocytes |
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