Coceani F, Bodach E, White E, Bishai I, Olley P M
Prostaglandins. 1978 Apr;15(4):551-6. doi: 10.1016/0090-6980(78)90051-5.
Prostaglandin (PG) I2 and its stable metabolite, 6-keto-PGF1alpha, were tested on the isolated ductus arteriosus from mature fetal lambs. PGI2 relaxed the ductus in high doses (threshold 10(-6)M) and its activity disappeared on standing at room temperature for 30 minutes. 6-keto-PGF1alpha was inactive at all doses. By contrast, PGE2 produced a dose-dependent relaxation over a range between 10(-10) and 10(-6)M. These findings confirm that PGE2 is the most potent ductal relaxant among the known derivatives of arachidonic acid. PGE2 probably maintains ductus patency in the fetus and, together with PGE1, remains the compound of choice in the management of newborns requiring a viable ductus for survival.
前列腺素(PG)I2及其稳定代谢产物6-酮-前列腺素F1α在成熟胎羊的离体动脉导管上进行了测试。PGI2在高剂量(阈值为10^(-6)M)时可使动脉导管松弛,且其活性在室温下静置30分钟后消失。6-酮-前列腺素F1α在所有剂量下均无活性。相比之下,前列腺素E2在10^(-10)至10^(-6)M的范围内产生剂量依赖性松弛。这些发现证实,前列腺素E2是已知花生四烯酸衍生物中最有效的动脉导管松弛剂。前列腺素E2可能维持胎儿动脉导管的通畅,并且与前列腺素E1一起,仍然是需要通过动脉导管存活的新生儿治疗中的首选化合物。