Hesse W H, Rudofsky G, Peskar B A
Institut für Pharmakologie und Toxikologie, Ruhr-Universität Bochum, Bundesrepublik Deutschland.
Wien Klin Wochenschr. 1991;103(18):554-7.
Using high performance liquid chromatography and radioimmunoassay we have investigated the stability of prostaglandin (PG) E1 and its metabolite 13,14-dihydro-PGE1 in human plasma as well as the initial metabolism of PGE1 infused intravenously (80 micrograms/patient/hour) in patients with peripheral arterial occlusive disease. 13,14-dihydro-PGE1 degraded like PGE1 in human plasma at 37 degrees C with a half-life of several hours. During infusion of PGE1 higher plasma concentrations of the major metabolite 15-keto-13,14-dihydro-PGE1 and lower plasma levels of PGE1 and 13,14-dihydro-PGE1 were observed. The metabolite 13,14-dihydro-PGE1 is of interest, since in contrast to 15-keto-13,14-dihydro-PGE1 it is biologically active. The biosynthesis of 13,14-dihydro-PGE1 could contribute to the therapeutic efficacy of PGE1 administered intravenously in patients with peripheral arterial occlusive disease.
我们使用高效液相色谱法和放射免疫分析法,研究了前列腺素(PG)E1及其代谢产物13,14-二氢-PGE1在人血浆中的稳定性,以及前列腺素E1(80微克/患者/小时)静脉输注到外周动脉闭塞性疾病患者体内后的初始代谢情况。13,14-二氢-PGE1在37℃的人血浆中与前列腺素E1一样降解,半衰期为几个小时。在输注前列腺素E1期间,观察到主要代谢产物15-酮-13,14-二氢-PGE1的血浆浓度较高,而前列腺素E1和13,14-二氢-PGE1的血浆水平较低。代谢产物13,14-二氢-PGE1值得关注,因为与15-酮-13,14-二氢-PGE1不同,它具有生物活性。13,14-二氢-PGE1的生物合成可能有助于静脉注射前列腺素E1对患有外周动脉闭塞性疾病患者的治疗效果。