Kinetic studies on the conversion of prostaglandin endoperoxide PGH2 by thromboxane synthase |
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Authors: | M.W. Anderson D.J. Crutchley B.E. Tainer T.E. Eling |
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Affiliation: | Laboratory of Pulmonary Function and Toxicology National Institute of Environmental Health Sciences P. O. Box 12233 Research Triangle Park, North Carolina 27709, USA |
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Abstract: | We have investigated the time course of formation of thromboxane A2, thromboxane B2, and the C-17 hydroxy fatty acid, HHT, from arachidonic acid in a washed human platelet suspension. Our results indicate that HHT is not a breakdown product of thromboxane A2, but rather thromboxane A2 decomposes exclusively into thromboxane B2. The kinetics of formation of thromboxane B2 from the endoperoxide prostaglandin H2 in human platelet microsomes was examined. Our data suggest that a bimolecular reaction is involved in the formation of thromboxane A2 from prostaglandin H2 and that thromboxane synthase is not an isomerase, but may be acting via a dismutase-type reaction. One possibility is that thromboxane and HHT are produced simultaneously from two molecules of prostaglandin H2. |
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