HYPOXIA AND CCL4-INDUCED LIVER-INJURY, BUT NOT ACIDOSIS, IMPAIR METABOLISM OF CYSTEINYL LEUKOTRIENES IN PERFUSED-RAT-LIVER

被引:7
作者
WETTSTEIN, M [1 ]
GEROK, W [1 ]
HAUSSINGER, D [1 ]
机构
[1] UNIV FREIBURG,MED KLIN,DEPT INTERNAL MED,HUGSTETTER STR 55,W-7800 FREIBURG,GERMANY
关键词
D O I
10.1002/hep.1840110523
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Uptake, metabolism and biliary elimination of infused cysteinyl leukotrienes were investigated in single‐pass perfused rat liver. Hypoxia did not impair uptake of infused [3H] leukotriene C4, but inhibited biliary excretion of radioactivity by about 50% compared with normoxic control experiments. In addition, the leukotriene metabolite pattern in bile was profoundly altered and was characterized in hypoxia by a 75% to 80% decrease of both leukotriene C4 and polar metabolites, representing ω‐oxidation products, whereas the appearance of leukotriene D4 in bile was not affected. Reoxygenation was followed by a marked increase of biliary excretion of polar metabolites, indicating that leukotrienes taken up and stored in the liver cells during the hypoxic period now underwent ω‐oxidation with subsequent slimination of the ω‐oxidized products. Hypoxia also inhibited the biliary excretion of radioactivity after [3H] leukotriene E4 addition because of an almost complete absence of ω‐oxidation products in bile, whereas N‐acetylleukotriene E4 excretion was not affected. Induction of liver injury by carbon tetrachloride treatment decreased single‐pass uptake of [3H] leukotriene C4 by 30%, and only 36% of the radioactivity taken up by the liver was eliminated into bile within 1 hr, compared with 78% in normal livers. The pattern of biliary leukotriene metabolites, however, was not significantly different. Lowering the pH in the perfusion medium from 7.4 to 7.1 had no effect on uptake, metabolism or biliary elimination of infused [3H] leukotriene C4. The data show that hypoxia and experimental liver injury, but not acidosis, impair hepatic processing of cysteinyl leukotriences. Thus, in leukotriene‐induced shock syndromes, leukotriene elimination and inactivation may be imnpaired giving rise to a “vicious circle.”(HEPATOLOGY 1990; 11:866‐873.) Copyright © 1990 American Association for the Study of Liver Diseases
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页码:866 / 873
页数:8
相关论文
共 34 条
[1]  
APPELGREN LE, 1982, J BIOL CHEM, V257, P531
[2]   OMEGA-OXIDATION PRODUCTS OF LEUKOTRIENE-E4 IN BILE AND URINE OF THE MONKEY [J].
BALL, HA ;
KEPPLER, D .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1987, 148 (02) :664-670
[3]  
Bergmeyer HU, 1974, METHODEN ENZYMATISCH
[4]  
DENZLINGER C, 1986, J BIOL CHEM, V261, P5601
[5]   COMPARATIVE AIRWAY AND VASCULAR ACTIVITIES OF LEUKOTRIENE-C-1 AND LEUKOTRIENE-D INVIVO AND INVITRO [J].
DRAZEN, JM ;
AUSTEN, KF ;
LEWIS, RA ;
CLARK, DA ;
GOTO, G ;
MARFAT, A ;
COREY, EJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1980, 77 (07) :4354-4358
[6]  
FITCH KA, 1983, CIRC SHOCK, V10, P51
[7]   EVIDENCE OF INVIVO W-OXIDATION OF PEPTIDE LEUKOTRIENES IN THE RAT - BILIARY-EXCRETION OF 20-CO2H N-ACETYL LTE4 [J].
FOSTER, A ;
FITZSIMMONS, B ;
ROKACH, J ;
LETTS, G .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1987, 148 (03) :1237-1245
[8]   ALTERATIONS OF HEPATIC ENZYME LEVELS AND OF THE ACINAR DISTRIBUTION OF GLUTAMINE-SYNTHETASE IN RESPONSE TO EXPERIMENTAL LIVER-INJURY IN THE RAT [J].
GEBHARDT, R ;
BURGER, HJ ;
HEINI, H ;
SCHREIBER, KL ;
MECKE, D .
HEPATOLOGY, 1988, 8 (04) :822-830
[9]   MORPHOLOGICAL-STUDIES ON SELECTIVE ACINAR LIVER-DAMAGE BY N-HYDROXY-2-ACETYLAMINOFLUORENE AND CARBON-TETRACHLORIDE [J].
GROOTHUIS, GMM ;
MEIJER, DKF ;
HARDONK, MJ .
NAUNYN-SCHMIEDEBERGS ARCHIVES OF PHARMACOLOGY, 1983, 322 (04) :298-309
[10]   PRODUCTION OF PEPTIDE LEUKOTRIENES IN ENDOTOXIN-SHOCK [J].
HAGMANN, W ;
DENZLINGER, C ;
KEPPLER, D .
FEBS LETTERS, 1985, 180 (02) :309-313