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Enterohepatic circulation of N-acetyl-leukotriene E4.

作者信息

Guhlmann A, Hagmann W, Keppler D

机构信息

Biochemisches Institut, Universität Freiburg, F.R.G.

出版信息

Prostaglandins. 1987 Jul;34(1):63-70. doi: 10.1016/0090-6980(87)90263-2.

DOI:10.1016/0090-6980(87)90263-2
PMID:3685398
Abstract

N-Acetyl-leukotriene E4, the end product of leukotriene C4 metabolism in the mercapturic acid pathway, was rapidly eliminated from the blood circulation into the bile of rats. Part of the N-acetyl-leukotriene E4 secreted from bile into the intestine underwent enterohepatic circulation. Leukotriene absorption occurred from the small intestine and from the colon. Biliary and urinary excretion within 5.5 h amounted to 15 and 2%, respectively, of the intraduodenally administered N-acetyl- 3H leukotriene E4 in animals anesthetized with ketamine. HPLC analyses indicated that 35% of the biliary radioactivity corresponded to unchanged N-acetyl-3H leukotriene E4, while 65% in bile and 100% in urine were polar metabolites. Enterohepatic circulation extends the biological half-life of N-acetyl-leukotriene E4.

摘要

相似文献

1
Enterohepatic circulation of N-acetyl-leukotriene E4.
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引用本文的文献

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[The Heinrich-Wieland Prize presentation. Metabolism and analysis of leukotrienes in vivo].[海因里希 - 维兰德奖颁奖仪式。白三烯在体内的代谢与分析]
Klin Wochenschr. 1988 Oct 17;66(20):997-1005. doi: 10.1007/BF01733441.
2
Prevention of endogenous leukotriene production during anaphylaxis in the guinea pig by an inhibitor of leukotriene biosynthesis (MK-886) but not by dexamethasone.白三烯生物合成抑制剂(MK - 886)可预防豚鼠过敏反应期间内源性白三烯的产生,但地塞米松则不能。
J Exp Med. 1989 Dec 1;170(6):1905-18. doi: 10.1084/jem.170.6.1905.