Swies J, Radomski M, Dembińska-Kieć A, Korbut R, Gryglewski R J, Brandt R, Nowak J
Eur J Clin Invest. 1985 Dec;15(6):320-6. doi: 10.1111/j.1365-2362.1985.tb00279.x.
The release of PGI2-like activity into the circulation in response to cholinergic agonists and modification of this response by beta-adrenergic antagonists was investigated in anaesthetized cats and healthy humans. Antiaggregatory activity in the arterial blood was continuously assayed by measuring platelet aggregation on blood superfused collagen strip. In some of the human experiments, after the administration of the drugs, the conversion of [14C]-arachidonate to [14C]-prostaglandins in the pulmonary vascular bed was studied. Cholinergic agonists stimulated the release of PGI2-like activity into the circulation, which effect was potentiated in cats by beta-adrenergic antagonists. In humans the latter agents did not stimulate the conversion of [14C]-arachidonate to prostaglandins in the pulmonary circulation and, moreover, inhibited the stimulatory cholinergic effect. The results suggest that an interplay between cholinergic and beta-adrenergic mediators may be involved, although in a different way in cats and in humans, in the release of PGI2-like activity into the systemic circulation.
在麻醉猫和健康人体中,研究了胆碱能激动剂刺激下类前列环素I2(PGI2)活性释放至循环系统以及β-肾上腺素能拮抗剂对该反应的影响。通过检测血液灌注胶原条上的血小板聚集情况,持续测定动脉血中的抗聚集活性。在部分人体实验中,给药后研究了肺血管床中[14C]-花生四烯酸向[14C]-前列腺素的转化。胆碱能激动剂刺激类PGI2活性释放至循环系统,在猫中β-肾上腺素能拮抗剂可增强该效应。在人体中,β-肾上腺素能拮抗剂不刺激肺循环中[14C]-花生四烯酸向前列腺素的转化,而且还抑制胆碱能激动剂的刺激作用。结果表明,胆碱能和β-肾上腺素能介质之间的相互作用可能参与了类PGI2活性释放至体循环的过程,不过在猫和人体中的方式不同。