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Distinct patterns of heparin affinity chromatography VLDL1 and VLDL2 subfractions in the different dyslipidaemias
Abstract Very low density lipoprotein (VLDL) 1 and 2 were fractionated by heparin affinity chromatography into a bound and an unbound fraction and the different subfractions were quantified in 17 normolipidaemic (NL), 13 hypercholesterolaemic (HC), 10 hypertriglyceridaemic (HTG) and 11 combined hype...
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Published in: | Atherosclerosis 2008-07, Vol.199 (1), p.27-33 |
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description | Abstract Very low density lipoprotein (VLDL) 1 and 2 were fractionated by heparin affinity chromatography into a bound and an unbound fraction and the different subfractions were quantified in 17 normolipidaemic (NL), 13 hypercholesterolaemic (HC), 10 hypertriglyceridaemic (HTG) and 11 combined hyperlipidaemic subjects (CHL). Unbound VLDL1 and VLDL2 were, respectively, 1.9- and 2.2-fold richer in triglycerides than bound VLDL1 and VLDL2. In HTG and CHL the concentration of all the VLDL subfractions was increased and plasma triglyceride level was correlated to unbound VLDL1 and to bound VLDL1 (respectively, r = 0.86 ( p < 0.001) and r = 0.77 ( p < 0.01) in HTG and r = 0.73 ( p < 0.001) and r = 0.62 ( p < 0.05) in CHL). In HC unbound VLDL2 and bound VLDL2 concentration were increased compared to NL and in CHL, the concentration of bound VLDL2 was particularly increased (3.2-fold compared to NL ( p < 0.001)). In both HC and CHL bound VLDL2 concentration was correlated to low density lipoprotein cholesterol (LDL-C) concentration (respectively, r = 0.67 ( p < 0.01) and r = 0.62 ( p < 0.05)). In hypertriglyceridaemic states the intravascular accumulation of both unbound and bound VLDL1 appears as the determinant of plasma triglyceride concentration, whereas in moderately hypercholesterolaemic states the concentration of bound VLDL2 is strikingly correlated to LDL-C concentration, suggesting that these two species are linked metabolically, e.g. bound VLDL2 contain the precursor pool of LDL. |
doi_str_mv | 10.1016/j.atherosclerosis.2007.11.026 |
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Unbound VLDL1 and VLDL2 were, respectively, 1.9- and 2.2-fold richer in triglycerides than bound VLDL1 and VLDL2. In HTG and CHL the concentration of all the VLDL subfractions was increased and plasma triglyceride level was correlated to unbound VLDL1 and to bound VLDL1 (respectively, r = 0.86 ( p < 0.001) and r = 0.77 ( p < 0.01) in HTG and r = 0.73 ( p < 0.001) and r = 0.62 ( p < 0.05) in CHL). In HC unbound VLDL2 and bound VLDL2 concentration were increased compared to NL and in CHL, the concentration of bound VLDL2 was particularly increased (3.2-fold compared to NL ( p < 0.001)). In both HC and CHL bound VLDL2 concentration was correlated to low density lipoprotein cholesterol (LDL-C) concentration (respectively, r = 0.67 ( p < 0.01) and r = 0.62 ( p < 0.05)). In hypertriglyceridaemic states the intravascular accumulation of both unbound and bound VLDL1 appears as the determinant of plasma triglyceride concentration, whereas in moderately hypercholesterolaemic states the concentration of bound VLDL2 is strikingly correlated to LDL-C concentration, suggesting that these two species are linked metabolically, e.g. bound VLDL2 contain the precursor pool of LDL.]]></description><identifier>ISSN: 0021-9150</identifier><identifier>EISSN: 1879-1484</identifier><identifier>DOI: 10.1016/j.atherosclerosis.2007.11.026</identifier><identifier>PMID: 18177876</identifier><language>eng</language><publisher>Amsterdam: Elsevier Ireland Ltd</publisher><subject>Adult ; Anticoagulants ; Apolipoproteins B - blood ; Atherosclerosis (general aspects, experimental research) ; Biological and medical sciences ; Blood and lymphatic vessels ; Blood. Blood coagulation. Reticuloendothelial system ; Cardiology. Vascular system ; Cardiovascular ; Chromatography, Affinity - methods ; Dyslipidemias - blood ; Female ; Heparin ; Heparin affinity chromatography ; Humans ; Hypercholesterolaemia ; Hypercholesterolemia - blood ; Hyperlipidemia, Familial Combined - blood ; Hypertriglyceridaemia ; Hypertriglyceridemia - blood ; Lipoproteins, VLDL - analysis ; Lipoproteins, VLDL - blood ; Lipoproteins, VLDL - isolation & purification ; Male ; Medical sciences ; Middle Aged ; Mixed hyperlipidaemia ; Pharmacology. Drug treatments ; Protein Binding ; Ultracentrifugation ; Very low density lipoprotein</subject><ispartof>Atherosclerosis, 2008-07, Vol.199 (1), p.27-33</ispartof><rights>Elsevier Ireland Ltd</rights><rights>2007 Elsevier Ireland Ltd</rights><rights>2008 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c538t-5ac1f8c14305ea47d119c5c04f134468ae1de34c70943edd54510201fcc64fda3</citedby><cites>FETCH-LOGICAL-c538t-5ac1f8c14305ea47d119c5c04f134468ae1de34c70943edd54510201fcc64fda3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=20487651$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18177876$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Duvillard, L</creatorcontrib><creatorcontrib>Caslake, M.J</creatorcontrib><creatorcontrib>Petit, J.M</creatorcontrib><creatorcontrib>Vergès, B</creatorcontrib><creatorcontrib>Gambert, P</creatorcontrib><creatorcontrib>Packard, C.J</creatorcontrib><title>Distinct patterns of heparin affinity chromatography VLDL1 and VLDL2 subfractions in the different dyslipidaemias</title><title>Atherosclerosis</title><addtitle>Atherosclerosis</addtitle><description><![CDATA[Abstract Very low density lipoprotein (VLDL) 1 and 2 were fractionated by heparin affinity chromatography into a bound and an unbound fraction and the different subfractions were quantified in 17 normolipidaemic (NL), 13 hypercholesterolaemic (HC), 10 hypertriglyceridaemic (HTG) and 11 combined hyperlipidaemic subjects (CHL). Unbound VLDL1 and VLDL2 were, respectively, 1.9- and 2.2-fold richer in triglycerides than bound VLDL1 and VLDL2. In HTG and CHL the concentration of all the VLDL subfractions was increased and plasma triglyceride level was correlated to unbound VLDL1 and to bound VLDL1 (respectively, r = 0.86 ( p < 0.001) and r = 0.77 ( p < 0.01) in HTG and r = 0.73 ( p < 0.001) and r = 0.62 ( p < 0.05) in CHL). In HC unbound VLDL2 and bound VLDL2 concentration were increased compared to NL and in CHL, the concentration of bound VLDL2 was particularly increased (3.2-fold compared to NL ( p < 0.001)). In both HC and CHL bound VLDL2 concentration was correlated to low density lipoprotein cholesterol (LDL-C) concentration (respectively, r = 0.67 ( p < 0.01) and r = 0.62 ( p < 0.05)). In hypertriglyceridaemic states the intravascular accumulation of both unbound and bound VLDL1 appears as the determinant of plasma triglyceride concentration, whereas in moderately hypercholesterolaemic states the concentration of bound VLDL2 is strikingly correlated to LDL-C concentration, suggesting that these two species are linked metabolically, e.g. bound VLDL2 contain the precursor pool of LDL.]]></description><subject>Adult</subject><subject>Anticoagulants</subject><subject>Apolipoproteins B - blood</subject><subject>Atherosclerosis (general aspects, experimental research)</subject><subject>Biological and medical sciences</subject><subject>Blood and lymphatic vessels</subject><subject>Blood. Blood coagulation. Reticuloendothelial system</subject><subject>Cardiology. Vascular system</subject><subject>Cardiovascular</subject><subject>Chromatography, Affinity - methods</subject><subject>Dyslipidemias - blood</subject><subject>Female</subject><subject>Heparin</subject><subject>Heparin affinity chromatography</subject><subject>Humans</subject><subject>Hypercholesterolaemia</subject><subject>Hypercholesterolemia - blood</subject><subject>Hyperlipidemia, Familial Combined - blood</subject><subject>Hypertriglyceridaemia</subject><subject>Hypertriglyceridemia - blood</subject><subject>Lipoproteins, VLDL - analysis</subject><subject>Lipoproteins, VLDL - blood</subject><subject>Lipoproteins, VLDL - isolation & purification</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Mixed hyperlipidaemia</subject><subject>Pharmacology. Drug treatments</subject><subject>Protein Binding</subject><subject>Ultracentrifugation</subject><subject>Very low density lipoprotein</subject><issn>0021-9150</issn><issn>1879-1484</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><recordid>eNqNkk2P1SAUhonRONfRv2DYjLtWTktLu9DEzOhochMXfmwJAwcv15Z2gJr030u915jMyoQAi-c95-QBQq6AlcCgfX0sVTpgmKIett3FsmJMlAAlq9pHZAed6AvgHX9MdoxVUPTQsAvyLMYjY4wL6J6SC-hAiE60O3J_42JyXic6q5Qw-EgnSw84q-A8VdY679JK9SFMo0rTj6Dmw0q_72_2QJU3f24VjcudDUonN-V8zuUJqXHWYkCfqFnj4GZnFI5OxefkiVVDxBfn85J8-_D-6_XHYv_59tP1u32hm7pLRaM02E4Dr1mDigsD0OtGM26h5rztFILBmmvBel6jMQ1vgFUMrNYtt0bVl-TVqe4cpvsFY5KjixqHQXmclijbvsplepHBNydQZ58xoJVzcKMKqwQmN-fyKB84l5tzCSCz85x_eW603I1o_qXPkjNwdQZU1GrIprzONf5yFeOZaiBztycOs5ZfDoOM2qHXaFxAnaSZ3H-P9PZBJT3kh8zNf-KK8TgtwWf3EmSsJJNfto-y_RMm8mo6Uf8G9FPABA</recordid><startdate>20080701</startdate><enddate>20080701</enddate><creator>Duvillard, L</creator><creator>Caslake, M.J</creator><creator>Petit, J.M</creator><creator>Vergès, B</creator><creator>Gambert, P</creator><creator>Packard, C.J</creator><general>Elsevier Ireland Ltd</general><general>Elsevier</general><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>20080701</creationdate><title>Distinct patterns of heparin affinity chromatography VLDL1 and VLDL2 subfractions in the different dyslipidaemias</title><author>Duvillard, L ; Caslake, M.J ; Petit, J.M ; Vergès, B ; Gambert, P ; Packard, C.J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c538t-5ac1f8c14305ea47d119c5c04f134468ae1de34c70943edd54510201fcc64fda3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Adult</topic><topic>Anticoagulants</topic><topic>Apolipoproteins B - blood</topic><topic>Atherosclerosis (general aspects, experimental research)</topic><topic>Biological and medical sciences</topic><topic>Blood and lymphatic vessels</topic><topic>Blood. Blood coagulation. Reticuloendothelial system</topic><topic>Cardiology. Vascular system</topic><topic>Cardiovascular</topic><topic>Chromatography, Affinity - methods</topic><topic>Dyslipidemias - blood</topic><topic>Female</topic><topic>Heparin</topic><topic>Heparin affinity chromatography</topic><topic>Humans</topic><topic>Hypercholesterolaemia</topic><topic>Hypercholesterolemia - blood</topic><topic>Hyperlipidemia, Familial Combined - blood</topic><topic>Hypertriglyceridaemia</topic><topic>Hypertriglyceridemia - blood</topic><topic>Lipoproteins, VLDL - analysis</topic><topic>Lipoproteins, VLDL - blood</topic><topic>Lipoproteins, VLDL - isolation & purification</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Mixed hyperlipidaemia</topic><topic>Pharmacology. Drug treatments</topic><topic>Protein Binding</topic><topic>Ultracentrifugation</topic><topic>Very low density lipoprotein</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Duvillard, L</creatorcontrib><creatorcontrib>Caslake, M.J</creatorcontrib><creatorcontrib>Petit, J.M</creatorcontrib><creatorcontrib>Vergès, B</creatorcontrib><creatorcontrib>Gambert, P</creatorcontrib><creatorcontrib>Packard, C.J</creatorcontrib><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>Atherosclerosis</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Duvillard, L</au><au>Caslake, M.J</au><au>Petit, J.M</au><au>Vergès, B</au><au>Gambert, P</au><au>Packard, C.J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Distinct patterns of heparin affinity chromatography VLDL1 and VLDL2 subfractions in the different dyslipidaemias</atitle><jtitle>Atherosclerosis</jtitle><addtitle>Atherosclerosis</addtitle><date>2008-07-01</date><risdate>2008</risdate><volume>199</volume><issue>1</issue><spage>27</spage><epage>33</epage><pages>27-33</pages><issn>0021-9150</issn><eissn>1879-1484</eissn><abstract><![CDATA[Abstract Very low density lipoprotein (VLDL) 1 and 2 were fractionated by heparin affinity chromatography into a bound and an unbound fraction and the different subfractions were quantified in 17 normolipidaemic (NL), 13 hypercholesterolaemic (HC), 10 hypertriglyceridaemic (HTG) and 11 combined hyperlipidaemic subjects (CHL). Unbound VLDL1 and VLDL2 were, respectively, 1.9- and 2.2-fold richer in triglycerides than bound VLDL1 and VLDL2. In HTG and CHL the concentration of all the VLDL subfractions was increased and plasma triglyceride level was correlated to unbound VLDL1 and to bound VLDL1 (respectively, r = 0.86 ( p < 0.001) and r = 0.77 ( p < 0.01) in HTG and r = 0.73 ( p < 0.001) and r = 0.62 ( p < 0.05) in CHL). In HC unbound VLDL2 and bound VLDL2 concentration were increased compared to NL and in CHL, the concentration of bound VLDL2 was particularly increased (3.2-fold compared to NL ( p < 0.001)). In both HC and CHL bound VLDL2 concentration was correlated to low density lipoprotein cholesterol (LDL-C) concentration (respectively, r = 0.67 ( p < 0.01) and r = 0.62 ( p < 0.05)). In hypertriglyceridaemic states the intravascular accumulation of both unbound and bound VLDL1 appears as the determinant of plasma triglyceride concentration, whereas in moderately hypercholesterolaemic states the concentration of bound VLDL2 is strikingly correlated to LDL-C concentration, suggesting that these two species are linked metabolically, e.g. bound VLDL2 contain the precursor pool of LDL.]]></abstract><cop>Amsterdam</cop><pub>Elsevier Ireland Ltd</pub><pmid>18177876</pmid><doi>10.1016/j.atherosclerosis.2007.11.026</doi><tpages>7</tpages></addata></record> |
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subjects | Adult Anticoagulants Apolipoproteins B - blood Atherosclerosis (general aspects, experimental research) Biological and medical sciences Blood and lymphatic vessels Blood. Blood coagulation. Reticuloendothelial system Cardiology. Vascular system Cardiovascular Chromatography, Affinity - methods Dyslipidemias - blood Female Heparin Heparin affinity chromatography Humans Hypercholesterolaemia Hypercholesterolemia - blood Hyperlipidemia, Familial Combined - blood Hypertriglyceridaemia Hypertriglyceridemia - blood Lipoproteins, VLDL - analysis Lipoproteins, VLDL - blood Lipoproteins, VLDL - isolation & purification Male Medical sciences Middle Aged Mixed hyperlipidaemia Pharmacology. Drug treatments Protein Binding Ultracentrifugation Very low density lipoprotein |
title | Distinct patterns of heparin affinity chromatography VLDL1 and VLDL2 subfractions in the different dyslipidaemias |
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