Nikolov R, Nikolova M, Miyares C, Milanova D
Methods Find Exp Clin Pharmacol. 1982;4(4):211-9.
The anti-hypoxic effect of prostacyclin (PGI2) was studied using the following methods: hypoventilation hypoxia and hypovolemic oligemia in cats and hypobaric hypoxia and complete ischemia by decapitation in mice. In experiments on cats PGI2 (250 ng/kg/min i.v.) led to an improvement of hypoxia-impaired EEG activity. In hypobaric hypoxia, PGI2 at all doses applied (50-500 micrograms/kg) led to a significant increase in the survival time (from 67.5% to 196%). In complete ischemia by decapitation, PGI2 at doses from 50 to 500 micrograms/kg significantly prolonged the gasping movements (from 7.8% to 20.6%). Different mechanisms of the anti-hypoxic effect of PGI2 are discussed. The effect observed would be potentially beneficial in hypoxic and ischemic states.
采用以下方法研究前列环素(PGI2)的抗缺氧作用:猫的低通气性缺氧和低血容量性低氧血症,以及小鼠的低压性缺氧和断头致完全缺血。在猫的实验中,PGI2(静脉注射,250 ng/kg/min)可改善缺氧损伤的脑电图活动。在低压性缺氧实验中,所有应用剂量(50 - 500微克/千克)的PGI2均可显著延长存活时间(从67.5%增至196%)。在断头致完全缺血实验中,50至500微克/千克剂量的PGI2可显著延长喘息运动时间(从7.8%增至20.6%)。文中讨论了PGI2抗缺氧作用的不同机制。观察到的这种作用在缺氧和缺血状态下可能具有潜在益处。