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白三烯B4在大鼠体内的肝脏摄取及代谢情况

Hepatic uptake and metabolic disposition of leukotriene B4 in rats.

作者信息

Hagmann W, Korte M

机构信息

Division of Tumor Biochemistry, Deutsches Krebsforschungszentrum, Heidelberg, Federal Republic of Germany.

出版信息

Biochem J. 1990 Apr 15;267(2):467-70. doi: 10.1042/bj2670467.

Abstract
  1. In isolated perfused rat liver and in vivo, up to 25% of [3H]leukotriene B4 was eliminated from the circulation via hepatic uptake and biliary excretion within 1 h. Total body recovery of 3H amounted to about 60% of infused [3H]leukotriene B4. 2. Hepatobiliary excretion of leukotriene B4 and its metabolites exceeded renal elimination by about 4-fold and depended, in contrast with excretion of cysteinyl leukotriene E4, upon continuous taurocholate supply. 3. Analyses of bile, liver and recirculated perfusate using h.p.l.c. indicated that the liver metabolized leukotriene B4 extensively to omega-carboxyleukotriene B4 and its beta-oxidized derivatives, and no unmetabolized leukotriene B4 appeared in bile. These results substantiate the important contribution of the hepatobiliary system with respect to the metabolic fate of leukotriene B4.
摘要
  1. 在离体灌注大鼠肝脏和体内,1小时内高达25%的[3H]白三烯B4通过肝脏摄取和胆汁排泄从循环中清除。3H的全身回收率约为注入的[3H]白三烯B4的60%。2. 白三烯B4及其代谢产物的肝胆排泄比肾脏排泄约高4倍,与半胱氨酰白三烯E4的排泄不同,它依赖于持续供应牛磺胆酸盐。3. 使用高效液相色谱法分析胆汁、肝脏和再循环灌注液表明,肝脏将白三烯B4广泛代谢为ω-羧基白三烯B4及其β-氧化衍生物,胆汁中未出现未代谢的白三烯B4。这些结果证实了肝胆系统对白三烯B4代谢命运的重要贡献。

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Leukotriene B4 metabolism by hepatic cytochrome P-450.肝脏细胞色素P-450对白三烯B4的代谢
Biochem Biophys Res Commun. 1983 Jul 29;114(2):850-4. doi: 10.1016/0006-291x(83)90859-8.
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Leukotrienes as mediators in tissue trauma.白三烯作为组织创伤中的介质。
Science. 1985 Oct 18;230(4723):330-2. doi: 10.1126/science.4048937.

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