Omini C, Moncada S, Vane J R
Prostaglandins. 1977 Oct;14(4):625-32. doi: 10.1016/0090-6980(77)90189-7.
The effects of prostacyclin (PGI2) and its stable metabolite 6-oxo-PGF1alpha on various bioassay tissues are compared with those of PGE2 and PGF2alpha, using the cascade superfusion method. On vascular smooth muscle, PGI2 caused relaxation of all tissues tested except the rabbit aorta. PGE2 relaxed rabbit coeliac and mesenteric artery but contracted bovine coronary artery and had no effect on rabbit aorta. 6-oxo-PGF1alpha was ineffective at the concentrations tested. On gastro-intestinal smooth muscle, PGI2 contracted strips of rat and hamster stomach and the chick rectum. It was less potent than PGE2 or PGF2alpha. None of these substances contracted the cat terminal ileum. 6-oxo-PGF1alpha was inactive on these tissues at the doses tested. PGI2 was less active than PGE2 or PGF2alpha in contracting guinea-pig trachea and rat uterus; 6-oxo-PGF1alpha was active only on the rat uterus. Thus, PGI2 can be distinguished from the other stable prostaglandins using the cascade method of superfusion.
采用级联超灌注法,将前列环素(PGI2)及其稳定代谢产物6-氧代-PGF1α对各种生物测定组织的作用与PGE2和PGF2α的作用进行比较。在血管平滑肌上,PGI2使除兔主动脉外的所有受试组织松弛。PGE2使兔腹腔动脉和肠系膜动脉松弛,但使牛冠状动脉收缩,对兔主动脉无影响。在所测试的浓度下,6-氧代-PGF1α无作用。在胃肠道平滑肌上,PGI2使大鼠和仓鼠胃条以及鸡直肠收缩。其效力低于PGE2或PGF2α。这些物质均未使猫末端回肠收缩。在所测试的剂量下,6-氧代-PGF1α对这些组织无活性。在收缩豚鼠气管和大鼠子宫方面,PGI2的活性低于PGE2或PGF2α;6-氧代-PGF1α仅对大鼠子宫有活性。因此,使用级联超灌注法可将PGI2与其他稳定的前列腺素区分开来。