Protection by Osbeckia aspera against carbon tetrachloride-mediated alterations in microsomal drug metabolizing enzyme activity

被引:0
作者
Jayatilaka, KAPW
Thabrew, MI
机构
[1] Univ Ruhuna, Fac Med, Dept Biochem, Matara, Sri Lanka
[2] Univ Kelaniya, Fac Med, Dept Biochem & Clin Chem, Kelaniya, Sri Lanka
关键词
D O I
10.1211/0022357001774084
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Previous investigations have confirmed the protective effect of Osbeckia aspera leaf extract on carbon tetrachloride-mediated liver injury in rat models. It is well known that the earliest alterations in liver cell structure and function following carbon tetrachloride poisoning involve the endoplasmic reticulum and its drug metabolizing enzymes. Therefore, we investigated whether an aqueous leaf extract of O. aspera could offer protection against carbon tetrachloride-induced changes in the microsomal drug metabolizing enzymes aniline hydroxylase and p-aminopyrine N-demethylase. This enzyme activity was compared with phenobarbital-induced righting reflex and lipid peroxidation. Treatment of rats with the aqueous leaf extract of O. aspera (before or after the administration of carbon tetrachloride) resulted in a marked decrease in carbon tetrachloride-mediated alterations in aniline hydroxylase and p-aminopyrine N-demethylase activity, phenobarbital-induced loss of righting reflex and malondialdehyde formation due to lipid peroxidation. The K-m value of these enzymes in control and Osbeckia-treated rats were the same. These results show that the plant extract can markedly decrease the carbon tetrachloride-mediated reduction in aniline hydroxylase and p-aminopyrine N-demethylase activity and inhibit peroxidative damage to the cell membrane. Phenobarbital-induced sleeping time in rats and kinetic enzyme studies suggested that the effects of the plant extract was neither due to an induction of the drug-metabolizing enzymes under investigation, nor due to an alteration in the K-m values of these enzymes.
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页码:461 / 465
页数:5
相关论文
共 28 条
[1]   THE INVOLVEMENT OF IRON AND LIPID-PEROXIDATION IN THE PATHOGENESIS OF HCB INDUCED PORPHYRIA [J].
ALLEMAN, MA ;
KOSTER, JF ;
WILSON, JHP ;
EDIXHOVENBOSDIJK, A ;
SLEE, RG ;
KROOS, MJ ;
VANEIJK, HG .
BIOCHEMICAL PHARMACOLOGY, 1985, 34 (02) :161-166
[2]   ENZYMATIC METABOLISM OF DRUGS AND OTHER FOREIGN COMPOUNDS [J].
BRODIE, BB ;
GILLETTE, JR ;
LADU, BN .
ANNUAL REVIEW OF BIOCHEMISTRY, 1958, 27 :427-454
[3]   PREVENTION OF CARBON TETRACHLORIDE-INDUCED NECROSIS BY INHIBITORS OF DRUG-METABOLISM - FURTHER STUDIES ON THEIR MECHANISM OF ACTION [J].
CASTRO, JA ;
FERREYRA, EC ;
CASTRO, CRD ;
FENOS, OMD ;
SASAME, H ;
GILLETTE, JR .
BIOCHEMICAL PHARMACOLOGY, 1974, 23 (02) :295-&
[4]  
CONNEY AH, 1972, FUNDAMENTALS DRUG ME, P253
[5]  
FASIER FN, 1957, BRIT J PHARM CHEMOTH, V12, P251
[6]  
Houghton P. J., 1993, Journal of Pharmacy and Pharmacology, V45, P1102
[7]  
JAYATILAKA KAP, 1991, THESI U RUHUA SRI LA
[8]   EFFECT OF MELOTHRIA-MADERASPATANA ON CARBON TETRACHLORIDE-INDUCED CHANGES IN RAT HEPATIC-MICROSOMAL DRUG-METABOLIZING ENZYME-ACTIVITY [J].
JAYATILAKA, KAPW ;
THABREW, MI ;
PERERA, DJB .
JOURNAL OF ETHNOPHARMACOLOGY, 1990, 30 (01) :97-105
[9]   SIMPLE PROCEDURE FOR ISOLATION OF RAT LIVER MICROSOMES [J].
KAMATH, SA ;
KUMMEROW, FA ;
NARAYAN, KA .
FEBS LETTERS, 1971, 17 (01) :90-&
[10]   ANTIHEPATOTOXIC EFFECTS OF CHLOROGENIC ACID FROM ANTHOCEPHALUS-CADAMBA [J].
KAPIL, A ;
KOUL, IB ;
SURI, OP .
PHYTOTHERAPY RESEARCH, 1995, 9 (03) :189-193