Lippton H L, Paustian P W, Mellion B T, Nelson P K, Feigen L P, Chapnick B M, Hyman A L, Kadowitz P J
Arch Int Pharmacodyn Ther. 1979 Sep;241(1):121-30.
The cardiovascular actions of the newly discovered bicyclic prostaglandin, prostacyclin, or PGI2, were compared with those of PGE1 in the anesthetized cat. PGI2 decreased systemic arterial pressure, increased cardiac output and decreased systemic vascular resistance. The decreases in systemic vascular resistance were similar when PGI2 was injected into the left or right atrium, suggesting that prostacyclin is not inactivated in the feline pulmonary vascular bed. PGE1 also decreased systemic arterial pressure and increased cardiac output; however, left atrial administration of this substance produced greater reductions in systemic vascular resistance than right atrial injections, suggesting that PGE1 is inactivated in the feline lung. PGI2 also caused dose-related decreases in perfusion pressure in the renal, hindquarters and mesenteric vascular beds and had the greatest vasodilator activity in the mesenteric vascular bed. PGE1 decreased perfusion pressure in the 3 regional beds, and the overall dilator effects of PGI2 and PGE1 in the peripheral circulation were quite smiliar. The present data show that PGI2 is a potent peripheral vasodilator in the cat and since this substance is not inactivated in the lung, it could serve as a circulating hormone in this species.
在麻醉猫身上,将新发现的双环前列腺素前列环素(PGI2)的心血管作用与前列腺素E1(PGE1)的作用进行了比较。PGI2可降低体动脉压,增加心输出量,并降低体循环血管阻力。当将PGI2注入左心房或右心房时,体循环血管阻力的降低情况相似,这表明前列环素在猫的肺血管床中不会失活。PGE1也可降低体动脉压并增加心输出量;然而,将该物质注入左心房比注入右心房能使体循环血管阻力有更大程度的降低,这表明PGE1在猫肺中会失活。PGI2还会使肾、后肢和肠系膜血管床的灌注压呈剂量相关下降,且在肠系膜血管床中具有最大的血管舒张活性。PGE1可降低这三个区域血管床的灌注压,PGI2和PGE1在体循环中的总体舒张作用相当相似。目前的数据表明,PGI2在猫体内是一种强效的外周血管舒张剂,并且由于该物质在肺中不会失活,它可能作为该物种的一种循环激素发挥作用。