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Validation of deuterium-labeled fatty acids for the measurement of dietary fat oxidation during physical activity
Measurement of 13C-labeled fatty acid oxidation is hindered by the need for acetate correction, measurement of the rate of CO2 production in a controlled environment, and frequent collection of breath samples. The use of deuterium-labeled fatty acids may overcome these limitations. Herein, d31-palmi...
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Published in: | Journal of lipid research 2004-12, Vol.45 (12), p.2339-2344 |
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description | Measurement of 13C-labeled fatty acid oxidation is hindered by the need for acetate correction, measurement of the rate of CO2 production in a controlled environment, and frequent collection of breath samples. The use of deuterium-labeled fatty acids may overcome these limitations. Herein, d31-palmitate was validated against [1-13C]palmitate during exercise. Thirteen subjects with body mass index of 22.9 ± 3 kg/m2 and body fat of 19.6 ± 11% were subjected to 2 or 4 h of exercise at 25% maximum volume oxygen consumption (VO2max). The d31-palmitate and [1-13C] palmitate were given orally in a liquid meal at breakfast. The d3-acetate and [1-13C]acetate were given during another visit for acetate sequestration correction. Recovery of d31-palmitate in urine at 9 h after dose was compared with [1-13C] palmitate recovery in breath. Cumulative recovery of d31-palmitate was 10.6 ± 3% and that of [1-13C]palmitate was 5.6 ± 2%. The d3-acetate and [1-13C]acetate recoveries were 85 ± 4% and 54 ± 4%, respectively. When [1-13C]acetate recovery was used to correct 13C data, the average recovery differences were 0.4 ± 3%. Uncorrected d31-palmitate and acetate-corrected [1-13C]palmitate were well correlated (y = 0.96x + 0; P < 0.0001) when used to measure fatty acid oxidation during exercise.
Thus, d31-palmitate can be used in outpatient settings as it eliminates the need for acetate correction and frequent sampling. |
doi_str_mv | 10.1194/jlr.M400289-JLR200 |
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Thus, d31-palmitate can be used in outpatient settings as it eliminates the need for acetate correction and frequent sampling.</description><identifier>ISSN: 0022-2275</identifier><identifier>EISSN: 1539-7262</identifier><identifier>DOI: 10.1194/jlr.M400289-JLR200</identifier><identifier>PMID: 15342677</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Acetic Acid - metabolism ; Deuterium - metabolism ; Dietary Fats - metabolism ; Exercise - physiology ; Fatty Acids - metabolism ; Female ; Humans ; isotope labeling ; lipid metabolism ; Male ; mass spectrometry ; Oxidation-Reduction ; Palmitic Acid - metabolism ; stable isotopes ; substrate utilization ; validity</subject><ispartof>Journal of lipid research, 2004-12, Vol.45 (12), p.2339-2344</ispartof><rights>2004 © 2004 ASBMB. Currently published by Elsevier Inc; originally published by American Society for Biochemistry and Molecular Biology.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c515t-ee3d42fb498981f35d423a07f1bdcfeca6337bfa25ca1ff6a62e9f45c7c6b61f3</citedby><cites>FETCH-LOGICAL-c515t-ee3d42fb498981f35d423a07f1bdcfeca6337bfa25ca1ff6a62e9f45c7c6b61f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0022227520341146$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>314,780,784,3549,27924,27925,45780</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15342677$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Raman, Aarthi</creatorcontrib><creatorcontrib>Blanc, Stephane</creatorcontrib><creatorcontrib>Adams, Alexandra</creatorcontrib><creatorcontrib>Schoeller, Dale A.</creatorcontrib><title>Validation of deuterium-labeled fatty acids for the measurement of dietary fat oxidation during physical activity</title><title>Journal of lipid research</title><addtitle>J Lipid Res</addtitle><description>Measurement of 13C-labeled fatty acid oxidation is hindered by the need for acetate correction, measurement of the rate of CO2 production in a controlled environment, and frequent collection of breath samples. The use of deuterium-labeled fatty acids may overcome these limitations. Herein, d31-palmitate was validated against [1-13C]palmitate during exercise. Thirteen subjects with body mass index of 22.9 ± 3 kg/m2 and body fat of 19.6 ± 11% were subjected to 2 or 4 h of exercise at 25% maximum volume oxygen consumption (VO2max). The d31-palmitate and [1-13C] palmitate were given orally in a liquid meal at breakfast. The d3-acetate and [1-13C]acetate were given during another visit for acetate sequestration correction. Recovery of d31-palmitate in urine at 9 h after dose was compared with [1-13C] palmitate recovery in breath. Cumulative recovery of d31-palmitate was 10.6 ± 3% and that of [1-13C]palmitate was 5.6 ± 2%. The d3-acetate and [1-13C]acetate recoveries were 85 ± 4% and 54 ± 4%, respectively. When [1-13C]acetate recovery was used to correct 13C data, the average recovery differences were 0.4 ± 3%. Uncorrected d31-palmitate and acetate-corrected [1-13C]palmitate were well correlated (y = 0.96x + 0; P < 0.0001) when used to measure fatty acid oxidation during exercise.
Thus, d31-palmitate can be used in outpatient settings as it eliminates the need for acetate correction and frequent sampling.</description><subject>Acetic Acid - metabolism</subject><subject>Deuterium - metabolism</subject><subject>Dietary Fats - metabolism</subject><subject>Exercise - physiology</subject><subject>Fatty Acids - metabolism</subject><subject>Female</subject><subject>Humans</subject><subject>isotope labeling</subject><subject>lipid metabolism</subject><subject>Male</subject><subject>mass spectrometry</subject><subject>Oxidation-Reduction</subject><subject>Palmitic Acid - metabolism</subject><subject>stable isotopes</subject><subject>substrate utilization</subject><subject>validity</subject><issn>0022-2275</issn><issn>1539-7262</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><sourceid>DOA</sourceid><recordid>eNp9kUGP1CAUx4nRuLOjX8CD9uStK1Ba2sSL2azumjEm6nolr_CYZdKWWaAb59vLbEe9mZAQ4Pd-PPgT8orRC8Y68W43hIsvglLeduXnzTdO6ROyYnXVlZI3_ClZ5SNeci7rM3Ie445SJkTDnpOzDAneSLki9z9hcAaS81PhbWFwThjcPJYD9DigKSykdChAOxML60OR7rAYEeIccMQpPRY5TBAOR7Twv_7YzBzctC32d4foNAxZkdyDS4cX5JmFIeLL07wmtx-vflxel5uvn24uP2xKXbM6lYiVEdz2omu7ltmqzqsKqLSsN9qihqaqZG-B1xqYtQ00HDsrai110ze5YE1uFq_xsFP74Mbco_Lg1OOGD1sFITk9oMJOdFSKPpupEFUNAoFXvWwNF6ymR9fbxbUP_n7GmNToosZhgAn9HFUjaVuLts0gX0AdfIwB7d-LGVXH0FQOTZ1CU0touej1yT73I5p_JaeUMvBmASx4Bdvgorr9zimrKO1kV-WxJu8XAvOPPjgMKmqHk0bjAuqUn-z-18Fv6CGzng</recordid><startdate>20041201</startdate><enddate>20041201</enddate><creator>Raman, Aarthi</creator><creator>Blanc, Stephane</creator><creator>Adams, Alexandra</creator><creator>Schoeller, Dale A.</creator><general>Elsevier Inc</general><general>Elsevier</general><scope>6I.</scope><scope>AAFTH</scope><scope>FBQ</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><scope>DOA</scope></search><sort><creationdate>20041201</creationdate><title>Validation of deuterium-labeled fatty acids for the measurement of dietary fat oxidation during physical activity</title><author>Raman, Aarthi ; Blanc, Stephane ; Adams, Alexandra ; Schoeller, Dale A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c515t-ee3d42fb498981f35d423a07f1bdcfeca6337bfa25ca1ff6a62e9f45c7c6b61f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Acetic Acid - metabolism</topic><topic>Deuterium - metabolism</topic><topic>Dietary Fats - metabolism</topic><topic>Exercise - physiology</topic><topic>Fatty Acids - metabolism</topic><topic>Female</topic><topic>Humans</topic><topic>isotope labeling</topic><topic>lipid metabolism</topic><topic>Male</topic><topic>mass spectrometry</topic><topic>Oxidation-Reduction</topic><topic>Palmitic Acid - metabolism</topic><topic>stable isotopes</topic><topic>substrate utilization</topic><topic>validity</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Raman, Aarthi</creatorcontrib><creatorcontrib>Blanc, Stephane</creatorcontrib><creatorcontrib>Adams, Alexandra</creatorcontrib><creatorcontrib>Schoeller, Dale A.</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>AGRIS</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><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Journal of lipid research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Raman, Aarthi</au><au>Blanc, Stephane</au><au>Adams, Alexandra</au><au>Schoeller, Dale A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Validation of deuterium-labeled fatty acids for the measurement of dietary fat oxidation during physical activity</atitle><jtitle>Journal of lipid research</jtitle><addtitle>J Lipid Res</addtitle><date>2004-12-01</date><risdate>2004</risdate><volume>45</volume><issue>12</issue><spage>2339</spage><epage>2344</epage><pages>2339-2344</pages><issn>0022-2275</issn><eissn>1539-7262</eissn><abstract>Measurement of 13C-labeled fatty acid oxidation is hindered by the need for acetate correction, measurement of the rate of CO2 production in a controlled environment, and frequent collection of breath samples. The use of deuterium-labeled fatty acids may overcome these limitations. Herein, d31-palmitate was validated against [1-13C]palmitate during exercise. Thirteen subjects with body mass index of 22.9 ± 3 kg/m2 and body fat of 19.6 ± 11% were subjected to 2 or 4 h of exercise at 25% maximum volume oxygen consumption (VO2max). The d31-palmitate and [1-13C] palmitate were given orally in a liquid meal at breakfast. The d3-acetate and [1-13C]acetate were given during another visit for acetate sequestration correction. Recovery of d31-palmitate in urine at 9 h after dose was compared with [1-13C] palmitate recovery in breath. Cumulative recovery of d31-palmitate was 10.6 ± 3% and that of [1-13C]palmitate was 5.6 ± 2%. The d3-acetate and [1-13C]acetate recoveries were 85 ± 4% and 54 ± 4%, respectively. When [1-13C]acetate recovery was used to correct 13C data, the average recovery differences were 0.4 ± 3%. Uncorrected d31-palmitate and acetate-corrected [1-13C]palmitate were well correlated (y = 0.96x + 0; P < 0.0001) when used to measure fatty acid oxidation during exercise.
Thus, d31-palmitate can be used in outpatient settings as it eliminates the need for acetate correction and frequent sampling.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>15342677</pmid><doi>10.1194/jlr.M400289-JLR200</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Acetic Acid - metabolism Deuterium - metabolism Dietary Fats - metabolism Exercise - physiology Fatty Acids - metabolism Female Humans isotope labeling lipid metabolism Male mass spectrometry Oxidation-Reduction Palmitic Acid - metabolism stable isotopes substrate utilization validity |
title | Validation of deuterium-labeled fatty acids for the measurement of dietary fat oxidation during physical activity |
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