Peskar B A, Hesse W H, Rogatti W, Diehm C, Rudofsky G, Schweer H, Seyberth H W
Department of Pharmacology and Toxicology, Ruhr University, Bochum, FRG.
Prostaglandins. 1991 Mar;41(3):225-8. doi: 10.1016/0090-6980(91)90042-e.
Formation of 13,14-dihydro-prostaglandin (PG) E1 during intravenous infusions of PGE1 in patients with peripheral arterial occlusive disease was investigated. Using both high performance liquid chromatography (h.p.l.c.) combined with radioimmunoassay and gas chromatography/triple stage quadrupole mass spectrometry (GC/MS/MS) basal levels of 13,14-dihydro-PGE1 were found to be close to or below the detection limits of the assay methods. Levels of the PGE1 metabolite increased significantly during the infusion periods and decreased after their end. Since 13,14-dihydro-PGE1, in contrast to its precursors 15-keto-PGE1 and 15-keto-13,14-dihydro-PGE1, is biologically active, its formation could contribute to the beneficial effects of PGE1 administered intravenously in patients with peripheral arterial occlusive disease.
研究了外周动脉闭塞性疾病患者静脉输注前列腺素E1(PGE1)期间13,14-二氢前列腺素(PG)E1的形成情况。使用高效液相色谱(h.p.l.c.)结合放射免疫测定法以及气相色谱/三级四极杆质谱法(GC/MS/MS),发现13,14-二氢-PGE1的基础水平接近或低于检测方法的检测限。在输注期间,PGE1代谢物水平显著升高,输注结束后降低。由于13,14-二氢-PGE1与其前体15-酮基-PGE1和15-酮基-13,14-二氢-PGE1不同,具有生物活性,其形成可能有助于静脉注射PGE1对外周动脉闭塞性疾病患者产生有益效果。