FORMATION OF 13,14-DIHYDRO-PROSTAGLANDIN-E1 DURING INTRAVENOUS INFUSIONS OF PROSTAGLANDIN-E1 IN PATIENTS WITH PERIPHERAL ARTERIAL OCCLUSIVE DISEASE

被引:34
作者
PESKAR, BA
HESSE, WH
ROGATTI, W
DIEHM, C
RUDOFSKY, G
SCHWEER, H
SEYBERTH, HW
机构
[1] UNIV HEIDELBERG,DEPT INTERNAL MED,W-6900 HEIDELBERG,GERMANY
[2] SCHWARZ PHARMA AG,W-4019 MONHEIM,GERMANY
[3] UNIV ESSEN GESAMTHSCH,DEPT INTERNAL MED,W-4300 ESSEN 1,GERMANY
[4] UNIV MARBURG,CHILDRENS HOSP,W-3550 MARBURG,GERMANY
来源
PROSTAGLANDINS | 1991年 / 41卷 / 03期
关键词
D O I
10.1016/0090-6980(91)90042-E
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:225 / 228
页数:4
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