On the mechanism of the oxygenation of arachidonic acid by human platelet lipoxygenase |
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Authors: | M Hamberg G Hamberg |
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Affiliation: | Department of Chemistry Karolinska Institutet, S-104 01 Stockholm 60, Sweden |
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Abstract: | Formation of 12L-hydroxy-5,8,10,14-eicosatetraenoic acid from [10L-3H; 3-14C]arachidonic acid in suspensions of human platelets occurred with extensive loss of tritium and was accompanied by an isotope effect. These experiments showed that there is an antarafacial relation between the elimination of hydrogen from C-10 and insertion of oxygen at C-12 by human platelet lipoxygenase, and that the hydrogen elimination probably occurs as the initial step of the conversion. (Endo) peroxide intermediates formed by the fatty acid cyclo-oxygenase pathway activated platelet lipoxygenase. |
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Keywords: | EPA 5,8,11,14,17-eicosapentaenoic acid 12-HPETE 12L-hydroperoxy-5,8,10,14-eicosatetraenoic acid 12-HETE 12L-hydroxy-5,8,10,14-eicosatetraenoic acid 12-HHT 12L-hydroxy-5,8,10-heptadecatrienoic acid 12-HEP 12-hydroxy-5,8,10,14,17-eicosapentaenoic acid 12-HHTE 12-hydroxy-5,8,10,14-heptadecatetraenoic acid |
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