Paajanen H
Invest Radiol. 1984 May-Jun;19(3):216-20.
Pulmonary inactivation of prostaglandin E2 (PGE2) was investigated in isolated perfused rat lungs during infusion of ionic and nonionic radiographic contrast media (RCM). When 100 nmol of [14C]-PGE2 was infused slowly into the pulmonary circulation, the ionic ioglycamate decreased the metabolism of PGE2, but other ionic (diatrizoate and ioxaglate) and nonionic RCM (iopamidol and metrizamide) had no significant effect. When a smaller amount of [14C]-PGE2 (10 nmol) was injected as a bolus the metabolism of PGE2 was decreased also by diatrizoate and ioxaglate, but not by iopamidol. After a similar bolus injection of 10 nmol of [14C]-PGE2, the efflux of radioactivity from the lungs was increased by diatrizoate, ioglycamate and ioxaglate but remained unchanged by iopamidol and metrizamide. The RCM infusion did not change the perfusion pressure. The present study indicates that ionic RCM decrease the inactivation of PGE2 in rat lungs and thus possibly increase the circulating level of this prostaglandin.
在灌注离子型和非离子型放射造影剂(RCM)期间,对离体灌注大鼠肺中前列腺素E2(PGE2)的肺内失活情况进行了研究。当将100 nmol的[14C]-PGE2缓慢注入肺循环时,离子型碘海醇降低了PGE2的代谢,但其他离子型(泛影葡胺和碘克沙醇)和非离子型RCM(碘帕醇和甲泛葡胺)没有显著影响。当以推注方式注射较少量的[14C]-PGE2(10 nmol)时,泛影葡胺和碘克沙醇也降低了PGE2的代谢,但碘帕醇没有。在以推注方式类似地注射10 nmol的[14C]-PGE2后,泛影葡胺、碘海醇和碘克沙醇增加了肺中放射性的流出,但碘帕醇和甲泛葡胺使其保持不变。RCM灌注未改变灌注压力。本研究表明,离子型RCM降低了大鼠肺中PGE2的失活,从而可能提高这种前列腺素的循环水平。