Abstract

[5,6,8,9,11,12,14,15- 3H 8]-Thromboxane B 2 was injected into the saphenous vein of female cynomolgus monkeys, and blood samples were withdrawn from the contralateral saphenous vein. The compound was eliminated from the circulation with a half-life of about 10 min after an initial rapid disappearnace. Some more polar products appeared with time, and also small amounts of material less polar than thromboxane B 2; however, the dominating compound in all blood samples was unconverted thromboxane B 2. About 45% of the given dose of tritium was excreted into urine in 48 hrs. Several metabolites of thromboxane B 2 were found. The major urinary metabolites was identified as dinorthromboxane B 2 (about 32% of urinary radioactivity). Unconverted thromboxane B 2 was also found in considerable amounts (13% of urinary radioactivity). It is concluded that 1) dehydrogenation at C-12 is not a major pathway in the degradation of this compound, in contrast to metabolism at the corresponding C-15 alcohol group of prostaglandins; 2) after having gained access to the circulation, thromboxane B 2 is the main circulating compound; however, assay of thromboxane B 2 in plasma will be complicated or precluded by large artifactual production of the compound by platelets during sample collection.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.