Salmon J A, Mullane K M, Dusting G J, Moncada S, Vane J R
J Pharm Pharmacol. 1979 Aug;31(8):529-32. doi: 10.1111/j.2042-7158.1979.tb13577.x.
The plasma concentration of 6-oxo-PGF1 alpha was measured by radioimmunoassay after constant rate infusion of 6-oxo-PGF1 alpha or prostacyclin (PGI2) into anaesthetized dogs. A steady-state plasma concentration was rapidly attained with both compounds. After termination of the infusions, the concentration of 6-oxo-PGF1 alpha declined according to a bi-exponential process. The steady-state plasma concentrations of 6-oxo-PGF1 alpha obtained after infusion of 6-oxo-PGF1 alpha and PGI2 were approximately 10 times higher than the corresponding steady-state level of PGF2 alpha measured after infusion of PGF2 alph into the same dogs. The data presented suggest that PGI2 and 6-oxo-PGF1 alpha are eliminated more slowly than PGF2 alpha, probably because they are not taken up and metabolized in the lungs as rapidly as PGF2 alpha.
在对麻醉犬持续恒速输注6-氧代-PGF1α或前列环素(PGI2)后,采用放射免疫分析法测定血浆中6-氧代-PGF1α的浓度。两种化合物均能迅速达到稳态血浆浓度。输注终止后,6-氧代-PGF1α的浓度按照双指数过程下降。对同一只犬输注6-氧代-PGF1α和PGI2后获得的6-氧代-PGF1α稳态血浆浓度,比输注PGF2α后测得的PGF2α相应稳态水平高约10倍。所呈现的数据表明,PGI2和6-氧代-PGF1α的消除速度比PGF2α慢,可能是因为它们不像PGF2α那样迅速被肺摄取和代谢。