13-Hydroxyoctadeca-9,11-dienoic acid (13-HODE) inhibits thromboxane A2 synthesis, and stimulates 12-HETE production in human platelets

The effect of 13-hydroxyoctadeca-9,11-dienoic acid (13-HODE), a major lipoxygenase product of endothelial cell linoleic acid metabolism on thrombin-induced platelet thromboxane B2 (TxB2), and 12-hydroxyeico-satetraenoic acid (12-HETE) production was evaluated. 13-HODE inhibited thrombin-induced TxB2...

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Veröffentlicht in:Biochemical and biophysical research communications 1987-10, Vol.148 (2), p.528-533
Hauptverfasser: YAMAJA SETTY, B. N, BERGER, M, STUART, M. J
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container_end_page 533
container_issue 2
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container_title Biochemical and biophysical research communications
container_volume 148
creator YAMAJA SETTY, B. N
BERGER, M
STUART, M. J
description The effect of 13-hydroxyoctadeca-9,11-dienoic acid (13-HODE), a major lipoxygenase product of endothelial cell linoleic acid metabolism on thrombin-induced platelet thromboxane B2 (TxB2), and 12-hydroxyeico-satetraenoic acid (12-HETE) production was evaluated. 13-HODE inhibited thrombin-induced TxB2 production in human platelets in a concentration-dependent manner. At concentrations of 10 and 30 microM, 13-HODE inhibited TxB2 production by 28 +/- 8% (1SE, n = 5; P less than 0.05) and 48 +/- 6% (P less than 0.01) respectively. 13-HODE (30 microM) also inhibited the production of platelet hydroxyheptadecatrienoic acid (38 +/- 5%, P less than 0.01). A concomitant stimulation of 12-HETE production by 13-HODE was observed (25 +/- 5% and 49 +/- 22% over control values at 10 and 30 microM respectively, P less than 0.01). Our results demonstrate a differential effect of 13-HODE on thrombin stimulated platelet cyclooxygenase and lipoxygenase metabolites.
doi_str_mv 10.1016/0006-291X(87)90908-9
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J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>13-Hydroxyoctadeca-9,11-dienoic acid (13-HODE) inhibits thromboxane A2 synthesis, and stimulates 12-HETE production in human platelets</atitle><jtitle>Biochemical and biophysical research communications</jtitle><addtitle>Biochem Biophys Res Commun</addtitle><date>1987-10-29</date><risdate>1987</risdate><volume>148</volume><issue>2</issue><spage>528</spage><epage>533</epage><pages>528-533</pages><issn>0006-291X</issn><eissn>1090-2104</eissn><coden>BBRCA9</coden><abstract>The effect of 13-hydroxyoctadeca-9,11-dienoic acid (13-HODE), a major lipoxygenase product of endothelial cell linoleic acid metabolism on thrombin-induced platelet thromboxane B2 (TxB2), and 12-hydroxyeico-satetraenoic acid (12-HETE) production was evaluated. 13-HODE inhibited thrombin-induced TxB2 production in human platelets in a concentration-dependent manner. At concentrations of 10 and 30 microM, 13-HODE inhibited TxB2 production by 28 +/- 8% (1SE, n = 5; P less than 0.05) and 48 +/- 6% (P less than 0.01) respectively. 13-HODE (30 microM) also inhibited the production of platelet hydroxyheptadecatrienoic acid (38 +/- 5%, P less than 0.01). A concomitant stimulation of 12-HETE production by 13-HODE was observed (25 +/- 5% and 49 +/- 22% over control values at 10 and 30 microM respectively, P less than 0.01). Our results demonstrate a differential effect of 13-HODE on thrombin stimulated platelet cyclooxygenase and lipoxygenase metabolites.</abstract><cop>San Diego, CA</cop><pub>Elsevier</pub><pmid>3120708</pmid><doi>10.1016/0006-291X(87)90908-9</doi><tpages>6</tpages></addata></record>
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subjects 12-Hydroxy-5,8,10,14-eicosatetraenoic Acid
Adult
Antithrombins - pharmacology
Applied sciences
Arachidonic Acid
Arachidonic Acids - blood
Blood Platelets - drug effects
Blood Platelets - metabolism
Exact sciences and technology
Humans
Hydroxyeicosatetraenoic Acids - biosynthesis
Hydroxyeicosatetraenoic Acids - blood
Kinetics
Linoleic Acids - pharmacology
Other techniques and industries
Phospholipids - biosynthesis
Phospholipids - blood
Platelet Aggregation
Thromboxane B2 - biosynthesis
Thromboxane B2 - blood
title 13-Hydroxyoctadeca-9,11-dienoic acid (13-HODE) inhibits thromboxane A2 synthesis, and stimulates 12-HETE production in human platelets
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