Guhlmann A, Krauss K, Oberdorfer F, Siegel T, Scheuber P H, Müller J, Csuk-Glänzer B, Ziegler S, Ostertag H, Keppler D
Deutsches Krebsforschungszentrum, Heidelberg, Germany.
Hepatology. 1995 Jun;21(6):1568-75.
N-Acetyl-leukotriene E4 has been identified as an endogenous, biologically less active cysteinyl leukotriene metabolite in rodents and humans. To evaluate the ratio of hepatobiliary to renal elimination of leukotrienes noninvasively by positron emission tomography (PET), we synthesized N-[11C]acetyl-leukotriene E4 by chemical N-acetylation of leukotriene E4. After the intravenous injection of N-[11C]acetyl-leukotriene E4 in normal rats and monkey, uptake by the liver and subsequent excretion into bile were largely responsible for its rapid elimination from blood. In the Cynomolgus monkey, renal excretion of the leukotriene into urine was of additional quantitative importance. Kinetic modeling indicated a mean transit time through the liver of 17 minutes and 34 minutes in rat and monkey, respectively; the corresponding hepatic excretion half-times amounted to 8.5 minutes and 16 minutes. In a mutant rat strain deficient in the hepatobiliary excretion of cysteinyl leukotrienes across the canalicular membrane, the apparent mean liver transit time was 54 minutes, and the hepatic excretion half-time was 29 minutes, indicating prolonged organ storage and metabolism. After transport from the liver back into the circulating blood of omega-oxidized and beta-oxidized metabolites of N-[11C]acetyl-leukotriene E4, renal excretion compensated for the impairment of hepatobiliary elimination in the transport mutant. Metabolite analyses in urine after intravenous injection of N-[3H]acetyl-leukotriene E4 indicated the extensive inactivation of N-acetyl-leukotriene E4 by beta-oxidation from the omega-end in the mutants. A similar shift from hepatobiliary to renal cysteinyl leukotriene elimination was monitored in rats with cholestasis due to bile duct obstruction.(ABSTRACT TRUNCATED AT 250 WORDS)
N-乙酰白三烯E4已被确定为啮齿动物和人类体内一种内源性、生物活性较低的半胱氨酰白三烯代谢产物。为了通过正电子发射断层扫描(PET)非侵入性评估白三烯在肝胆和肾脏消除的比例,我们通过对白三烯E4进行化学N-乙酰化合成了N-[11C]乙酰白三烯E4。在正常大鼠和猴子静脉注射N-[11C]乙酰白三烯E4后,肝脏摄取及随后向胆汁中的排泄在很大程度上导致了其从血液中的快速消除。在食蟹猴中,白三烯向尿液中的肾脏排泄在数量上也具有重要意义。动力学模型表明,在大鼠和猴子中,通过肝脏的平均转运时间分别为17分钟和34分钟;相应的肝脏排泄半衰期分别为8.5分钟和16分钟。在一种缺乏半胱氨酰白三烯经胆小管膜进行肝胆排泄的突变大鼠品系中,表观平均肝脏转运时间为54分钟,肝脏排泄半衰期为29分钟,表明器官储存和代谢时间延长。在N-[11C]乙酰白三烯E4的ω-氧化和β-氧化代谢产物从肝脏转运回循环血液后,肾脏排泄弥补了转运突变体中肝胆消除的损害。静脉注射N-[3H]乙酰白三烯E4后尿液中的代谢产物分析表明,突变体中N-乙酰白三烯E4通过从ω端进行β-氧化而广泛失活。在因胆管阻塞而发生胆汁淤积的大鼠中,也监测到了从肝胆向肾脏消除半胱氨酰白三烯的类似转变。(摘要截短于250字)