Effect of Interesterification of Palmitic Acid-rich Triacylglycerol on Postprandial Lipid and Factor VII Response
The process of interesterification results in changes in triacylglycerol (TAG) structure and is used to increase the melting point of dietary fats. The acute health effects of this process on palmitic acid-rich fats are uncertain with regard to postprandial lipemia, insulin and factor VII activated...
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Veröffentlicht in: | Lipids 2007-04, Vol.42 (4), p.315-323 |
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description | The process of interesterification results in changes in triacylglycerol (TAG) structure and is used to increase the melting point of dietary fats. The acute health effects of this process on palmitic acid-rich fats are uncertain with regard to postprandial lipemia, insulin and factor VII activated (FVIIa) concentrations. Two randomized crossover trials in healthy male subjects compared the effects of meals containing 50 g fat [interesterified palm oil (IPO) versus native palm oil (NPO); n = 20, and IPO versus high-oleic sunflower oil (HOS); n = 18], on postprandial changes in lipids, glucose, insulin, chylomicron composition and FVIIa. Compared with NPO, IPO decreased postprandial TAG and insulin concentrations. Both NPO and IPO increased FVIIa concentrations postprandially; mean increases at 6 h were 21 and 19%, respectively. Compared with HOS, IPO decreased postprandial TAG (47% lower incremental area under the curve) and reduced the postprandial increase in FVIIa concentration by 64% at 6 h; no significant differences in hepatic and total lipase activities or insulin concentrations were noted. All three test meals increased postprandial leukocyte counts (average 26% at 6 h). The fatty acid composition of the chylomicron TAG was similar to the test fats following all test meals. It is concluded that interesterification of palm oil does not result in adverse changes in postprandial lipids, insulin or FVIIa compared to high oleate and native palm oils. |
doi_str_mv | 10.1007/s11745-007-3024-x |
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E ; Woodward, Rebecca ; Yeoh, Christabelle ; Miller, George J ; Sanders, Thomas A. B</creator><creatorcontrib>Berry, Sarah E. E ; Woodward, Rebecca ; Yeoh, Christabelle ; Miller, George J ; Sanders, Thomas A. B</creatorcontrib><description>The process of interesterification results in changes in triacylglycerol (TAG) structure and is used to increase the melting point of dietary fats. The acute health effects of this process on palmitic acid-rich fats are uncertain with regard to postprandial lipemia, insulin and factor VII activated (FVIIa) concentrations. Two randomized crossover trials in healthy male subjects compared the effects of meals containing 50 g fat [interesterified palm oil (IPO) versus native palm oil (NPO); n = 20, and IPO versus high-oleic sunflower oil (HOS); n = 18], on postprandial changes in lipids, glucose, insulin, chylomicron composition and FVIIa. Compared with NPO, IPO decreased postprandial TAG and insulin concentrations. Both NPO and IPO increased FVIIa concentrations postprandially; mean increases at 6 h were 21 and 19%, respectively. Compared with HOS, IPO decreased postprandial TAG (47% lower incremental area under the curve) and reduced the postprandial increase in FVIIa concentration by 64% at 6 h; no significant differences in hepatic and total lipase activities or insulin concentrations were noted. All three test meals increased postprandial leukocyte counts (average 26% at 6 h). The fatty acid composition of the chylomicron TAG was similar to the test fats following all test meals. It is concluded that interesterification of palm oil does not result in adverse changes in postprandial lipids, insulin or FVIIa compared to high oleate and native palm oils.</description><identifier>ISSN: 0024-4201</identifier><identifier>EISSN: 1558-9307</identifier><identifier>DOI: 10.1007/s11745-007-3024-x</identifier><identifier>PMID: 17406926</identifier><language>eng</language><publisher>Berlin/Heidelberg: Berlin/Heidelberg : Springer-Verlag</publisher><subject>Adolescent ; Adult ; Blood Glucose - metabolism ; Chylomicron composition ; Chylomicrons - metabolism ; Cross-Over Studies ; dietary fat ; Dietary Fats - administration & dosage ; Dietary Fats - pharmacology ; esterification ; Esters ; Factor VII - metabolism ; human nutrition ; Humans ; Insulin ; Insulin - blood ; Insulin - metabolism ; Leukocytes - cytology ; Leukocytes - drug effects ; Leukocytes - metabolism ; Lipase activity ; Lipid Metabolism - drug effects ; Lipids ; Lipids - chemistry ; Male ; Melting point ; Middle Aged ; Palm Oil ; palmitic acid ; Palmitic Acid - chemistry ; Plant Oils - administration & dosage ; Plant Oils - pharmacology ; Postprandial lipemia ; Postprandial Period ; postprandial state ; Sunflower Oil ; triacylglycerols ; Triglycerides - administration & dosage ; Triglycerides - chemistry ; Triglycerides - pharmacology ; White blood cells</subject><ispartof>Lipids, 2007-04, Vol.42 (4), p.315-323</ispartof><rights>2007 American Oil Chemists' Society (AOCS)</rights><rights>Copyright AOCS Press Apr 2007</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3135-7e83b759159a0803eef73aca8be1ed409301448243b0b8b25db817b8a2c0a7c13</citedby><cites>FETCH-LOGICAL-c3135-7e83b759159a0803eef73aca8be1ed409301448243b0b8b25db817b8a2c0a7c13</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1007%2Fs11745-007-3024-x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1007%2Fs11745-007-3024-x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,777,781,1412,27905,27906,45555,45556</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17406926$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Berry, Sarah E. E</creatorcontrib><creatorcontrib>Woodward, Rebecca</creatorcontrib><creatorcontrib>Yeoh, Christabelle</creatorcontrib><creatorcontrib>Miller, George J</creatorcontrib><creatorcontrib>Sanders, Thomas A. B</creatorcontrib><title>Effect of Interesterification of Palmitic Acid-rich Triacylglycerol on Postprandial Lipid and Factor VII Response</title><title>Lipids</title><addtitle>Lipids</addtitle><description>The process of interesterification results in changes in triacylglycerol (TAG) structure and is used to increase the melting point of dietary fats. The acute health effects of this process on palmitic acid-rich fats are uncertain with regard to postprandial lipemia, insulin and factor VII activated (FVIIa) concentrations. Two randomized crossover trials in healthy male subjects compared the effects of meals containing 50 g fat [interesterified palm oil (IPO) versus native palm oil (NPO); n = 20, and IPO versus high-oleic sunflower oil (HOS); n = 18], on postprandial changes in lipids, glucose, insulin, chylomicron composition and FVIIa. Compared with NPO, IPO decreased postprandial TAG and insulin concentrations. Both NPO and IPO increased FVIIa concentrations postprandially; mean increases at 6 h were 21 and 19%, respectively. Compared with HOS, IPO decreased postprandial TAG (47% lower incremental area under the curve) and reduced the postprandial increase in FVIIa concentration by 64% at 6 h; no significant differences in hepatic and total lipase activities or insulin concentrations were noted. All three test meals increased postprandial leukocyte counts (average 26% at 6 h). The fatty acid composition of the chylomicron TAG was similar to the test fats following all test meals. It is concluded that interesterification of palm oil does not result in adverse changes in postprandial lipids, insulin or FVIIa compared to high oleate and native palm oils.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Blood Glucose - metabolism</subject><subject>Chylomicron composition</subject><subject>Chylomicrons - metabolism</subject><subject>Cross-Over Studies</subject><subject>dietary fat</subject><subject>Dietary Fats - administration & dosage</subject><subject>Dietary Fats - pharmacology</subject><subject>esterification</subject><subject>Esters</subject><subject>Factor VII - metabolism</subject><subject>human nutrition</subject><subject>Humans</subject><subject>Insulin</subject><subject>Insulin - blood</subject><subject>Insulin - metabolism</subject><subject>Leukocytes - cytology</subject><subject>Leukocytes - drug effects</subject><subject>Leukocytes - metabolism</subject><subject>Lipase activity</subject><subject>Lipid Metabolism - drug effects</subject><subject>Lipids</subject><subject>Lipids - chemistry</subject><subject>Male</subject><subject>Melting point</subject><subject>Middle Aged</subject><subject>Palm Oil</subject><subject>palmitic acid</subject><subject>Palmitic Acid - chemistry</subject><subject>Plant Oils - administration & dosage</subject><subject>Plant Oils - pharmacology</subject><subject>Postprandial lipemia</subject><subject>Postprandial Period</subject><subject>postprandial state</subject><subject>Sunflower Oil</subject><subject>triacylglycerols</subject><subject>Triglycerides - administration & dosage</subject><subject>Triglycerides - chemistry</subject><subject>Triglycerides - pharmacology</subject><subject>White blood cells</subject><issn>0024-4201</issn><issn>1558-9307</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</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>eNqFkUtv3CAUhVGVqpkm_QHZNCiL7pyAgQEvozxaSyN1lEe3COPrlIgxDniUzL8vlkeK1E02cO_Vd464HIROKDmnhMiLRKnkoshlwUjJi7dPaEGFUEXFiDxACzINeUnoIfqa0nNuKa_EF3SYZWRZlcsFernpOrAjDh2u-xEipHy4zlkzutBP47XxGzc6iy-ta4vo7F_8EJ2xO__kdxZi8DiD65DGIZq-dcbjlRtci3ODb40dQ8R_6hrfQRpCn-AYfe6MT_Btfx-hx9ubh6tfxer3z_rqclVYRpkoJCjWSFFRURmiCAPoJDPWqAYotJzkFSnnquSsIY1qStE2ispGmdISIy1lR-jH7DvE8LLNe-mNSxa8Nz2EbdKSMM4EqzJ49h_4HLaxz2_TpeRSLDmfIDpDNoaUInR6iG5j4k5Toqcw9ByGnsopDP2WNd_3xttmA-27Yv_7GZAz8Oo87D521Kt6fU0YFVl5Ois7E7R5ii7px_scNMvwkqlSsX-o8561</recordid><startdate>200704</startdate><enddate>200704</enddate><creator>Berry, Sarah E. 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E</au><au>Woodward, Rebecca</au><au>Yeoh, Christabelle</au><au>Miller, George J</au><au>Sanders, Thomas A. B</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effect of Interesterification of Palmitic Acid-rich Triacylglycerol on Postprandial Lipid and Factor VII Response</atitle><jtitle>Lipids</jtitle><addtitle>Lipids</addtitle><date>2007-04</date><risdate>2007</risdate><volume>42</volume><issue>4</issue><spage>315</spage><epage>323</epage><pages>315-323</pages><issn>0024-4201</issn><eissn>1558-9307</eissn><abstract>The process of interesterification results in changes in triacylglycerol (TAG) structure and is used to increase the melting point of dietary fats. The acute health effects of this process on palmitic acid-rich fats are uncertain with regard to postprandial lipemia, insulin and factor VII activated (FVIIa) concentrations. Two randomized crossover trials in healthy male subjects compared the effects of meals containing 50 g fat [interesterified palm oil (IPO) versus native palm oil (NPO); n = 20, and IPO versus high-oleic sunflower oil (HOS); n = 18], on postprandial changes in lipids, glucose, insulin, chylomicron composition and FVIIa. Compared with NPO, IPO decreased postprandial TAG and insulin concentrations. Both NPO and IPO increased FVIIa concentrations postprandially; mean increases at 6 h were 21 and 19%, respectively. Compared with HOS, IPO decreased postprandial TAG (47% lower incremental area under the curve) and reduced the postprandial increase in FVIIa concentration by 64% at 6 h; no significant differences in hepatic and total lipase activities or insulin concentrations were noted. All three test meals increased postprandial leukocyte counts (average 26% at 6 h). The fatty acid composition of the chylomicron TAG was similar to the test fats following all test meals. It is concluded that interesterification of palm oil does not result in adverse changes in postprandial lipids, insulin or FVIIa compared to high oleate and native palm oils.</abstract><cop>Berlin/Heidelberg</cop><pub>Berlin/Heidelberg : Springer-Verlag</pub><pmid>17406926</pmid><doi>10.1007/s11745-007-3024-x</doi><tpages>9</tpages></addata></record> |
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subjects | Adolescent Adult Blood Glucose - metabolism Chylomicron composition Chylomicrons - metabolism Cross-Over Studies dietary fat Dietary Fats - administration & dosage Dietary Fats - pharmacology esterification Esters Factor VII - metabolism human nutrition Humans Insulin Insulin - blood Insulin - metabolism Leukocytes - cytology Leukocytes - drug effects Leukocytes - metabolism Lipase activity Lipid Metabolism - drug effects Lipids Lipids - chemistry Male Melting point Middle Aged Palm Oil palmitic acid Palmitic Acid - chemistry Plant Oils - administration & dosage Plant Oils - pharmacology Postprandial lipemia Postprandial Period postprandial state Sunflower Oil triacylglycerols Triglycerides - administration & dosage Triglycerides - chemistry Triglycerides - pharmacology White blood cells |
title | Effect of Interesterification of Palmitic Acid-rich Triacylglycerol on Postprandial Lipid and Factor VII Response |
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