Incorporation and washout of orally administered n-3 fatty acid ethyl esters in different plasma lipid fractions
The aim of the present study was to quantify the incorporation of eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA) into plasma lipids after oral administration of n-3 fatty acid ethyl esters, since little is known about the rate and pattern of incorporation into plasma lipid fractions. In...
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description | The aim of the present study was to quantify the incorporation of eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA) into plasma lipids after oral administration of n-3 fatty acid ethyl esters, since little is known about the rate and pattern of incorporation into plasma lipid fractions. In addition, we aimed to obtain preliminary information regarding EPA half-life, which is needed to establish an optimal dosing schedule. Five healthy volunteers ingested two 8·5 g doses of n-3 fatty acid ethyl esters daily for 7 d, supplying 6·0 g EPA/d and 5·3 g DHA/d. The fatty acid compositions of plasma phospholipids (PL), cholesteryl esters (CE) and triacylglycerols (TAG) were determined during supplementation and during a washout period of 7 d. Half-lives of EPA and DHA were calculated. The proportion of EPA in PL showed a 15-fold increase after 7 d (P < 0·001), while DHA showed a smaller increase (P < 0·01). In CE, EPA also increased (P < 0·05), while DHA did not increase at all. Remarkably, incorporation of DHA into TAG was even higher than that of EPA. Half-life of EPA in PL ranged from 1·63 to 2·31 d (mean 1·97 (se 0·15) d), whereas mean half-life of EPA in CE was 3·27 (se 0·56) d. In three subjects, washout of EPA and DHA from TAG seemed to follow a bi-exponential pattern, with a short half-life (< 1 d) in the initial phase and a half-life of several days in the second phase. In conclusion, EPA ethyl esters are rapidly incorporated into plasma lipids, especially into PL. The relatively long half-life of EPA in plasma would permit a dosing schedule with intervals of ≥12 h in supplementation studies. |
doi_str_mv | 10.1017/S0007114599001737 |
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H.</creator><creatorcontrib>Zuijdgeest-van Leeuwen, Sonja D. ; Dagnelie, Pieter C. ; Rietveld, Trinet ; van den Berg, J.Willem O. ; Paul Wilson, J. H.</creatorcontrib><description>The aim of the present study was to quantify the incorporation of eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA) into plasma lipids after oral administration of n-3 fatty acid ethyl esters, since little is known about the rate and pattern of incorporation into plasma lipid fractions. In addition, we aimed to obtain preliminary information regarding EPA half-life, which is needed to establish an optimal dosing schedule. Five healthy volunteers ingested two 8·5 g doses of n-3 fatty acid ethyl esters daily for 7 d, supplying 6·0 g EPA/d and 5·3 g DHA/d. The fatty acid compositions of plasma phospholipids (PL), cholesteryl esters (CE) and triacylglycerols (TAG) were determined during supplementation and during a washout period of 7 d. Half-lives of EPA and DHA were calculated. The proportion of EPA in PL showed a 15-fold increase after 7 d (P < 0·001), while DHA showed a smaller increase (P < 0·01). In CE, EPA also increased (P < 0·05), while DHA did not increase at all. Remarkably, incorporation of DHA into TAG was even higher than that of EPA. Half-life of EPA in PL ranged from 1·63 to 2·31 d (mean 1·97 (se 0·15) d), whereas mean half-life of EPA in CE was 3·27 (se 0·56) d. In three subjects, washout of EPA and DHA from TAG seemed to follow a bi-exponential pattern, with a short half-life (< 1 d) in the initial phase and a half-life of several days in the second phase. In conclusion, EPA ethyl esters are rapidly incorporated into plasma lipids, especially into PL. The relatively long half-life of EPA in plasma would permit a dosing schedule with intervals of ≥12 h in supplementation studies.</description><identifier>ISSN: 0007-1145</identifier><identifier>EISSN: 1475-2662</identifier><identifier>DOI: 10.1017/S0007114599001737</identifier><identifier>PMID: 10690163</identifier><identifier>CODEN: BJNUAV</identifier><language>eng</language><publisher>Cambridge, UK: Cambridge University Press</publisher><subject>Adult ; Analysis of Variance ; Biological and medical sciences ; Cholesterol Esters - chemistry ; Dietary Supplements ; Docosahexaenoic Acids - analysis ; Docosahexaenoic Acids - metabolism ; Docosahexaenoic Acids - pharmacokinetics ; Drug Administration Schedule ; Eicosapentaenoic Acid - analogs & derivatives ; Eicosapentaenoic Acid - analysis ; Eicosapentaenoic Acid - metabolism ; Eicosapentaenoic Acid - pharmacokinetics ; Ethyl esters ; Feeding. Feeding behavior ; Female ; Fundamental and applied biological sciences. Psychology ; Half-Life ; Humans ; Lipid Metabolism ; Male ; n-3 Fatty acids ; Phospholipids - chemistry ; Plasma lipids ; Triglycerides - chemistry ; Vertebrates: anatomy and physiology, studies on body, several organs or systems</subject><ispartof>British journal of nutrition, 1999-12, Vol.82 (6), p.481-488</ispartof><rights>Copyright © The Nutrition Society 1999</rights><rights>2000 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c408t-499605b3f9e04bd54b4067f0c9950c2bc5bf9b43e84c204972a972a2f57f23573</citedby><cites>FETCH-LOGICAL-c408t-499605b3f9e04bd54b4067f0c9950c2bc5bf9b43e84c204972a972a2f57f23573</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=1260554$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10690163$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zuijdgeest-van Leeuwen, Sonja D.</creatorcontrib><creatorcontrib>Dagnelie, Pieter C.</creatorcontrib><creatorcontrib>Rietveld, Trinet</creatorcontrib><creatorcontrib>van den Berg, J.Willem O.</creatorcontrib><creatorcontrib>Paul Wilson, J. H.</creatorcontrib><title>Incorporation and washout of orally administered n-3 fatty acid ethyl esters in different plasma lipid fractions</title><title>British journal of nutrition</title><addtitle>Br J Nutr</addtitle><description>The aim of the present study was to quantify the incorporation of eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA) into plasma lipids after oral administration of n-3 fatty acid ethyl esters, since little is known about the rate and pattern of incorporation into plasma lipid fractions. In addition, we aimed to obtain preliminary information regarding EPA half-life, which is needed to establish an optimal dosing schedule. Five healthy volunteers ingested two 8·5 g doses of n-3 fatty acid ethyl esters daily for 7 d, supplying 6·0 g EPA/d and 5·3 g DHA/d. The fatty acid compositions of plasma phospholipids (PL), cholesteryl esters (CE) and triacylglycerols (TAG) were determined during supplementation and during a washout period of 7 d. Half-lives of EPA and DHA were calculated. The proportion of EPA in PL showed a 15-fold increase after 7 d (P < 0·001), while DHA showed a smaller increase (P < 0·01). In CE, EPA also increased (P < 0·05), while DHA did not increase at all. Remarkably, incorporation of DHA into TAG was even higher than that of EPA. Half-life of EPA in PL ranged from 1·63 to 2·31 d (mean 1·97 (se 0·15) d), whereas mean half-life of EPA in CE was 3·27 (se 0·56) d. In three subjects, washout of EPA and DHA from TAG seemed to follow a bi-exponential pattern, with a short half-life (< 1 d) in the initial phase and a half-life of several days in the second phase. In conclusion, EPA ethyl esters are rapidly incorporated into plasma lipids, especially into PL. The relatively long half-life of EPA in plasma would permit a dosing schedule with intervals of ≥12 h in supplementation studies.</description><subject>Adult</subject><subject>Analysis of Variance</subject><subject>Biological and medical sciences</subject><subject>Cholesterol Esters - chemistry</subject><subject>Dietary Supplements</subject><subject>Docosahexaenoic Acids - analysis</subject><subject>Docosahexaenoic Acids - metabolism</subject><subject>Docosahexaenoic Acids - pharmacokinetics</subject><subject>Drug Administration Schedule</subject><subject>Eicosapentaenoic Acid - analogs & derivatives</subject><subject>Eicosapentaenoic Acid - analysis</subject><subject>Eicosapentaenoic Acid - metabolism</subject><subject>Eicosapentaenoic Acid - pharmacokinetics</subject><subject>Ethyl esters</subject><subject>Feeding. Feeding behavior</subject><subject>Female</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Half-Life</subject><subject>Humans</subject><subject>Lipid Metabolism</subject><subject>Male</subject><subject>n-3 Fatty acids</subject><subject>Phospholipids - chemistry</subject><subject>Plasma lipids</subject><subject>Triglycerides - chemistry</subject><subject>Vertebrates: anatomy and physiology, studies on body, several organs or systems</subject><issn>0007-1145</issn><issn>1475-2662</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kMuKFDEUhoMoTs_oA7iRLMRd6UlVLp2lNGPPwKDIqAs3IZVKnIyppEyq0H57U3SjguAihHP-79x-hJ4ReEWAiNe3ACAIoUxKqHEnHqANoYI1LeftQ7RZ5WbVz9B5Kfc13BKQj9EZAS6B8G6DputoUp5S1rNPEes44B-63KVlxsnhmg7hgPUw-ujLbLMdcGw67PQ817TxA7bz3SFgu4oF-4gH71zl4oynoMuocfBTxVzWZp1QnqBHTodin57-C_Tp7eXH3VVz835_vXtz0xgK27mhUnJgfeekBdoPjPYUuHBgpGRg2t6w3smednZLTQtUilavr3VMuLZjortAL499p5y-L3U_NfpibAg62rQUxSWlRHJZQXIETU6lZOvUlP2o80ERUKvN6h-ba83zU_OlH-3wV8XR1wq8OAG6GB3q9dH48odr63GMVqw5Yqu5P3_LOn9TvM5hiu8_qHf7HYgvn2_VynenXfXYZz98teo-LTlWI_-z7S-xhqNK</recordid><startdate>19991201</startdate><enddate>19991201</enddate><creator>Zuijdgeest-van Leeuwen, Sonja D.</creator><creator>Dagnelie, Pieter C.</creator><creator>Rietveld, Trinet</creator><creator>van den Berg, J.Willem O.</creator><creator>Paul Wilson, J. H.</creator><general>Cambridge University Press</general><scope>BSCLL</scope><scope>IQODW</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>19991201</creationdate><title>Incorporation and washout of orally administered n-3 fatty acid ethyl esters in different plasma lipid fractions</title><author>Zuijdgeest-van Leeuwen, Sonja D. ; Dagnelie, Pieter C. ; Rietveld, Trinet ; van den Berg, J.Willem O. ; Paul Wilson, J. H.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c408t-499605b3f9e04bd54b4067f0c9950c2bc5bf9b43e84c204972a972a2f57f23573</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1999</creationdate><topic>Adult</topic><topic>Analysis of Variance</topic><topic>Biological and medical sciences</topic><topic>Cholesterol Esters - chemistry</topic><topic>Dietary Supplements</topic><topic>Docosahexaenoic Acids - analysis</topic><topic>Docosahexaenoic Acids - metabolism</topic><topic>Docosahexaenoic Acids - pharmacokinetics</topic><topic>Drug Administration Schedule</topic><topic>Eicosapentaenoic Acid - analogs & derivatives</topic><topic>Eicosapentaenoic Acid - analysis</topic><topic>Eicosapentaenoic Acid - metabolism</topic><topic>Eicosapentaenoic Acid - pharmacokinetics</topic><topic>Ethyl esters</topic><topic>Feeding. Feeding behavior</topic><topic>Female</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Half-Life</topic><topic>Humans</topic><topic>Lipid Metabolism</topic><topic>Male</topic><topic>n-3 Fatty acids</topic><topic>Phospholipids - chemistry</topic><topic>Plasma lipids</topic><topic>Triglycerides - chemistry</topic><topic>Vertebrates: anatomy and physiology, studies on body, several organs or systems</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zuijdgeest-van Leeuwen, Sonja D.</creatorcontrib><creatorcontrib>Dagnelie, Pieter C.</creatorcontrib><creatorcontrib>Rietveld, Trinet</creatorcontrib><creatorcontrib>van den Berg, J.Willem O.</creatorcontrib><creatorcontrib>Paul Wilson, J. H.</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</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>Zuijdgeest-van Leeuwen, Sonja D.</au><au>Dagnelie, Pieter C.</au><au>Rietveld, Trinet</au><au>van den Berg, J.Willem O.</au><au>Paul Wilson, J. H.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Incorporation and washout of orally administered n-3 fatty acid ethyl esters in different plasma lipid fractions</atitle><jtitle>British journal of nutrition</jtitle><addtitle>Br J Nutr</addtitle><date>1999-12-01</date><risdate>1999</risdate><volume>82</volume><issue>6</issue><spage>481</spage><epage>488</epage><pages>481-488</pages><issn>0007-1145</issn><eissn>1475-2662</eissn><coden>BJNUAV</coden><abstract>The aim of the present study was to quantify the incorporation of eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA) into plasma lipids after oral administration of n-3 fatty acid ethyl esters, since little is known about the rate and pattern of incorporation into plasma lipid fractions. In addition, we aimed to obtain preliminary information regarding EPA half-life, which is needed to establish an optimal dosing schedule. Five healthy volunteers ingested two 8·5 g doses of n-3 fatty acid ethyl esters daily for 7 d, supplying 6·0 g EPA/d and 5·3 g DHA/d. The fatty acid compositions of plasma phospholipids (PL), cholesteryl esters (CE) and triacylglycerols (TAG) were determined during supplementation and during a washout period of 7 d. Half-lives of EPA and DHA were calculated. The proportion of EPA in PL showed a 15-fold increase after 7 d (P < 0·001), while DHA showed a smaller increase (P < 0·01). In CE, EPA also increased (P < 0·05), while DHA did not increase at all. Remarkably, incorporation of DHA into TAG was even higher than that of EPA. Half-life of EPA in PL ranged from 1·63 to 2·31 d (mean 1·97 (se 0·15) d), whereas mean half-life of EPA in CE was 3·27 (se 0·56) d. In three subjects, washout of EPA and DHA from TAG seemed to follow a bi-exponential pattern, with a short half-life (< 1 d) in the initial phase and a half-life of several days in the second phase. In conclusion, EPA ethyl esters are rapidly incorporated into plasma lipids, especially into PL. The relatively long half-life of EPA in plasma would permit a dosing schedule with intervals of ≥12 h in supplementation studies.</abstract><cop>Cambridge, UK</cop><pub>Cambridge University Press</pub><pmid>10690163</pmid><doi>10.1017/S0007114599001737</doi><tpages>8</tpages></addata></record> |
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subjects | Adult Analysis of Variance Biological and medical sciences Cholesterol Esters - chemistry Dietary Supplements Docosahexaenoic Acids - analysis Docosahexaenoic Acids - metabolism Docosahexaenoic Acids - pharmacokinetics Drug Administration Schedule Eicosapentaenoic Acid - analogs & derivatives Eicosapentaenoic Acid - analysis Eicosapentaenoic Acid - metabolism Eicosapentaenoic Acid - pharmacokinetics Ethyl esters Feeding. Feeding behavior Female Fundamental and applied biological sciences. Psychology Half-Life Humans Lipid Metabolism Male n-3 Fatty acids Phospholipids - chemistry Plasma lipids Triglycerides - chemistry Vertebrates: anatomy and physiology, studies on body, several organs or systems |
title | Incorporation and washout of orally administered n-3 fatty acid ethyl esters in different plasma lipid fractions |
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