Troxerutin protects the isolated perfused rat liver from a possible lipid peroxidation by coumarin

被引:29
作者
Adam, BS
Pentz, R
Siegers, CP
Strubelt, O
Tegtmeier, M [1 ]
机构
[1] Schaper & Brummer Gmbh, D-38259 Salzgitter, Germany
[2] Med Univ Lubeck, Inst Expt & Clin Pharmacol & Toxicol, D-23538 Lubeck, Germany
关键词
coumarin; troxerutin; cytochrome P450; lipid peroxidation; isolated perfused rat liver;
D O I
10.1016/j.phymed.2004.01.007
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
For more than 40 years coumarin has been successfully used in the therapy of chronic venous insufficiency (CVI). The occurrence of liver injuries is rather rare and happens predominantly when doses are administered which are significantly higher than necessary for therapeutical use. Such effects caused by high coumarin concentrations are reproducible in in vivo experiments in mice or rats and HepG2-cells. In order to characterize the mechanism of liver injuries, the isolated perfused rat liver has been chosen as model. Since liver injuries are quite rare, if coumarin is used in co-medication with troxerutin, a possible protective influence of this flavonoid has been investigated. In concentrations higher than 4 mmol/l, coumarin alone is effective in the isolated perfused rat liver. Then the release of the enzymes alanine aminotransferase (ALT) and lactate dehydrogenase (LDH) increases and there is a measurable reduction of perfusion flow, oxygen consumption and rate of bile secretion. Additionally, the concentrations of hepatic adenosine triphosphate (ATP) and oxidized and total glutathione (GSSG/GSH) decrease. In the livers of fasting animals, coumarin doubles the concentration of hepatic malondialdehyde (MDA). This effect cannot be detected if troxerutin is added. In general, troxerutin reduces the concentration of all coumarin-metabolites in the perfusate and bile and changes the ratio of the main metabolites, coumarin: 3-hydroxycoumarin: 7-hydroxycoumarin. An analysis of the metabolic steps also shows that the amount of coumarin eliminated via faeces does not stem from absorbed coumarin, because the amount of orally applied coumarin detectable in the bile is less than 1%. The study demonstrates that troxerutin has hepatoprotective properties and thus protects the liver from a possible lipid peroxidation caused by coumarin. However, it is necessary to point out that these adverse effects caused by coumarin can be detected only in very high concentrations considerably above the regular therapeutical dosage. This allows the conclusion that troxerutin is a beneficial cofactor in coumarin preparations used for the therapy of chronic venous insufficiency. (C) 2004 Elsevier GmbH. All rights reserved.
引用
收藏
页码:52 / 61
页数:10
相关论文
共 47 条
[1]  
ADAM A, 1995, N-S ARCH PHARMACOL, V351, pR55
[2]   THE EFFECT OF COUMARIN DERIVATIVES ON THE IMMUNOLOGICAL SYSTEM OF MAN [J].
BERKARDA, B ;
BOUFFARDEYUBOGLU, H ;
DERMAN, U .
AGENTS AND ACTIONS, 1983, 13 (01) :50-52
[3]  
BOISSEAU MR, 1995, J CARDIOVASC SURG, V36, P369
[4]  
Born SL, 1997, DRUG METAB DISPOS, V25, P1318
[5]   Naringenin and interindividual variability in interaction of coumarin with grapefruit juice [J].
Bourian, M ;
Runkel, M ;
Krisp, A ;
Tegtmeier, M ;
Freudenstein, J ;
Legrum, W .
EXPERIMENTAL AND TOXICOLOGIC PATHOLOGY, 1999, 51 (4-5) :289-293
[6]   ENZYMATIC ASSAY FOR GLUTATHIONE [J].
BREHE, JE ;
BURCH, HB .
ANALYTICAL BIOCHEMISTRY, 1976, 74 (01) :189-197
[7]  
BRUPPACHER N, 1997, ESOP S BERL
[8]  
Casley-Smith JR, 1999, INT ANGIOL, V18, P31
[9]   TREATMENT OF LYMPHEDEMA OF THE ARMS AND LEGS WITH 5,6-BENZO-[ALPHA]-PYRONE [J].
CASLEYSMITH, JR ;
MORGAN, RG ;
PILLER, NB .
NEW ENGLAND JOURNAL OF MEDICINE, 1993, 329 (16) :1158-1163
[10]   THE RARITY OF LIVER TOXICITY IN PATIENTS TREATED WITH COUMARIN (1,2-BENZOPYRONE) [J].
COX, D ;
OKENNEDY, R ;
THORNES, RD .
HUMAN TOXICOLOGY, 1989, 8 (06) :501-506