Source:http://linkedlifedata.com/resource/pubmed/id/14612451
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4
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pubmed:dateCreated |
2004-1-19
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pubmed:abstractText |
We have investigated the role of endothelial cells in the metabolism of 20-hydroxyeicosatetraenoic acid (20-HETE), a vasoactive mediator synthesized from arachidonic acid by cytochrome P450 omega-oxidases. Porcine coronary artery endothelial cells (PCEC) incorporated 20-[(3)H]HETE primarily into the sn-2 position of phospholipids through a coenzyme A-dependent process. The incorporation was reduced by equimolar amounts of arachidonic, eicosapentaenoic or 8,9-epoxyeicosatrienoic acids, but some uptake persisted even when a 10-fold excess of arachidonic acid was available. The retention of 20-[(3)H]HETE increased substantially when methyl arachidonoyl fluorophosphonate, but not bromoenol lactone, was added, suggesting that a Ca(2+)-dependent cytosolic phospholipase A(2) released the 20-HETE contained in PCEC phospholipids. Addition of calcium ionophore A23187 produced a rapid release of 20-[(3)H]HETE from the PCEC, a finding that also is consistent with a Ca(2+)-dependent mobilization process. PCEC also converted 20-[(3)H]HETE to 20-carboxy-arachidonic acid (20-COOH-AA) and 18-, 16-, and 14-carbon beta-oxidation products. 20-COOH-AA produced vasodilation in porcine coronary arterioles, but 20-HETE was inactive. These results suggest that the incorporation of 20-HETE and its subsequent conversion to 20-COOH-AA in the endothelium may be important in modulating coronary vascular function.
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pubmed:grant |
http://linkedlifedata.com/resource/pubmed/grant/GM31278,
http://linkedlifedata.com/resource/pubmed/grant/HL070860,
http://linkedlifedata.com/resource/pubmed/grant/HL51055,
http://linkedlifedata.com/resource/pubmed/grant/HL62984,
http://linkedlifedata.com/resource/pubmed/grant/HL72845,
http://linkedlifedata.com/resource/pubmed/grant/RR13799
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Jan
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pubmed:issn |
0021-9258
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pubmed:author |
pubmed-author:CampbellWilliam BWB,
pubmed-author:DellspergerKevin CKC,
pubmed-author:FalckJ RJR,
pubmed-author:FangXiangX,
pubmed-author:GopalV RajVR,
pubmed-author:HarmonShawn DSD,
pubmed-author:KaduceTerry LTL,
pubmed-author:OltmanChristine LCL,
pubmed-author:SpectorArthur AAA,
pubmed-author:TeeschLynn MLM,
pubmed-author:WeintraubNeal LNL
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pubmed:issnType |
Print
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pubmed:day |
23
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pubmed:volume |
279
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
2648-56
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:14612451-Animals,
pubmed-meshheading:14612451-Biological Transport, Active,
pubmed-meshheading:14612451-Calcimycin,
pubmed-meshheading:14612451-Coronary Vessels,
pubmed-meshheading:14612451-Endothelium, Vascular,
pubmed-meshheading:14612451-Hydroxyeicosatetraenoic Acids,
pubmed-meshheading:14612451-Ionophores,
pubmed-meshheading:14612451-Swine,
pubmed-meshheading:14612451-Time Factors
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pubmed:year |
2004
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pubmed:articleTitle |
20-hydroxyeicosatetraenoic acid (20-HETE) metabolism in coronary endothelial cells.
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pubmed:affiliation |
Department of Biochemistry, Carver College of Medicine, University of Iowa, Iowa City, Iowa 52242, USA.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, U.S. Gov't, Non-P.H.S.,
Research Support, Non-U.S. Gov't
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