Protein targets of xenobiotic reactive intermediates

被引:121
作者
Pumford, NR
Halmes, NC
机构
关键词
acetaminophen; halothane; protein adducts; protein-conjugates; trichloroethylene;
D O I
10.1146/annurev.pharmtox.37.1.91
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Many xenobiotics are metabolically activated to electrophilic intermediates that form covalent adducts with proteins; the mechanism of toxicity is either intrinsic or idiosyncratic in nature. Many intrinsic toxins covalently modify cellular proteins and somehow initiate a sequence of events that leads to toxicity. Major protein adducts of several intrinsic toxins have been identified and demonstrate significant decreases in enzymatic activity. The reactivity of intermediates and subcellular localization of major targets may be important in the toxicity. Idiosyncratic toxicities are mediated through either a metabolic or immune-mediated mechanism. Xenobiotics that cause hypersensitivity/autoimmunity appear to have a limited number of protein targets, which are localized within the subcellular fraction where the electrophile is produced, are highly substituted, and are accessible to the immune system. Metabolic idiosyncratic toxins appear to have limited targets and are localized within a specific subcellular fraction. Identification of protein targets has given us insights into mechanisms of xenobiotic toxicity.
引用
收藏
页码:91 / 117
页数:27
相关论文
共 167 条
[1]  
ALLEMAND H, 1978, J PHARMACOL EXP THER, V204, P714
[2]   PROCESSING OF ENDOPLASMIC-RETICULUM LUMINAL ANTIGENS ASSOCIATED WITH HALOTHANE HEPATITIS IN RAT HEPATOCYTES [J].
AMOUZADEH, HR ;
POHL, LR .
HEPATOLOGY, 1995, 22 (03) :936-943
[3]  
AMOUZADEH HR, 1996, IN PRESS CHEM RES TO
[4]   COVALENT PROTEIN MODIFICATIONS AND GENE-EXPRESSION CHANGES IN RODENT LIVER FOLLOWING ADMINISTRATION OF METHAPYRILENE - A STUDY USING 2-DIMENSIONAL ELECTROPHORESIS [J].
ANDERSON, NL ;
COPPLE, DC ;
BENDELE, RA ;
PROBST, GS ;
RICHARDSON, FC .
FUNDAMENTAL AND APPLIED TOXICOLOGY, 1992, 18 (04) :570-580
[5]   Chemical and immunochemical comparison of protein adduct formation of four carboxylate drugs in rat liver and plasma [J].
Bailey, MJ ;
Dickinson, RG .
CHEMICAL RESEARCH IN TOXICOLOGY, 1996, 9 (03) :659-666
[6]  
BANKS AT, 1995, HEPATOLOGY, V22, P820, DOI 10.1002/hep.1840220320
[7]  
BARRY RE, 1987, LIVER, V7, P364
[8]   IMMUNOCHEMICAL DETECTION OF ACETAMINOPHEN-BOUND LIVER PROTEINS [J].
BARTOLONE, JB ;
SPARKS, K ;
COHEN, SD ;
KHAIRALLAH, EA .
BIOCHEMICAL PHARMACOLOGY, 1987, 36 (08) :1193-1196
[9]   PURIFICATION, ANTIBODY-PRODUCTION, AND PARTIAL AMINO-ACID-SEQUENCE OF THE 58-KDA ACETAMINOPHEN-BINDING LIVER PROTEINS [J].
BARTOLONE, JB ;
BIRGE, RB ;
BULERA, SJ ;
BRUNO, MK ;
NISHANIAN, EV ;
COHEN, SD ;
KHAIRALLAH, EA .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 1992, 113 (01) :19-29
[10]   IMMUNOTOXICOLOGY AND EXPRESSION OF HUMAN CYTOCHROME-P450 IN MICROORGANISMS [J].
BEAUNE, P ;
BOURDI, M ;
BELLOC, C ;
GAUTIER, JC ;
GUENGERICH, FP ;
VALADON, P .
TOXICOLOGY, 1993, 82 (1-3) :53-60