NEPHROTOXIC AND GENOTOXIC N-ACETYL-S-DICHLOROVINYL-L-CYSTEINE IS A URINARY METABOLITE AFTER OCCUPATIONAL 1,1,2-TRICHLOROETHENE EXPOSURE IN HUMANS - IMPLICATIONS FOR THE RISK OF TRICHLOROETHENE EXPOSURE

被引:89
作者
BIRNER, G [1 ]
VAMVAKAS, S [1 ]
WOLFGANG, D [1 ]
HENSCHLER, D [1 ]
机构
[1] UNIV WURZBURG,INST TOXIKOL,VERSBACHER STR 9,W-8700 WURZBURG,GERMANY
关键词
D O I
10.2307/3431501
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Excretion of mercapturic acids in the urine is indicative of the formation of electrophiles in the metabolism of xenobiotics. The determination of these mercapturic acids thus may be a useful method to estimate the exposure. We identified the nephrotoxic and mutagenic mercapturic adds N-acetYl-S-(1,2-dichlorovinyl)-L-cysteine and N-acetyl-S- (2,2-dichloro-vinyl)-L-cysteine in the urine of workers exposed to 1,1,2-trichloroethene. A method to quantify these mercapturic acids by gas chromatography-mass spectrometry-selected ion monitoring was developed and appreciable amounts (2.8-3.8 mumole/L were found in human urine samples. Because deacetylation determines notably the amount of the excreted mercapturic acids, the formation of the resulting cysteine S-conjugates was comparably measured in subcellular fractions of rodent and human kidneys; significant species differences in acylase activity were found. The formation of mutagenic and nephrotoxic metabolites during 1,1,2-trichloroethene metabolism mandates a revision of the risk assessment of trichloroethene exposure.
引用
收藏
页码:281 / 284
页数:4
相关论文
共 8 条
[1]   IDENTIFICATION OF N-ACETYL(2,2-DICHLOROVINYL)-L-CYSTEINE AND N-ACETYL(1,2-DICHLOROVINYL)-L-CYSTEINE AS 2 REGIOISOMERIC MERCAPTURIC ACIDS OF TRICHLOROETHYLENE IN THE RAT [J].
COMMANDEUR, JNM ;
VERMEULEN, NPE .
CHEMICAL RESEARCH IN TOXICOLOGY, 1990, 3 (03) :212-218
[2]   METABOLISM OF TRICHLOROETHENE - INVIVO AND INVITRO EVIDENCE FOR ACTIVATION BY GLUTATHIONE CONJUGATION [J].
DEKANT, W ;
KOOB, M ;
HENSCHLER, D .
CHEMICO-BIOLOGICAL INTERACTIONS, 1990, 73 (01) :89-101
[3]   BACTERIAL BETA-LYASE MEDIATED CLEAVAGE AND MUTAGENICITY OF CYSTEINE CONJUGATES DERIVED FROM THE NEPHROCARCINOGENIC ALKENES TRICHLOROETHYLENE, TETRACHLOROETHYLENE AND HEXACHLOROBUTADIENE [J].
DEKANT, W ;
VAMVAKAS, S ;
BERTHOLD, K ;
SCHMIDT, S ;
WILD, D ;
HENSCHLER, D .
CHEMICO-BIOLOGICAL INTERACTIONS, 1986, 60 (01) :31-45
[4]  
DEKANT W, 1986, NEW CONCEPTS DEV TOX, P211
[5]   BIOCHEMICAL, HISTOLOGICAL, AND ULTRASTRUCTURAL-CHANGES IN RAT AND MOUSE-LIVER FOLLOWING THE ADMINISTRATION OF TRICHLOROETHYLENE - POSSIBLE RELEVANCE TO SPECIES-DIFFERENCES IN HEPATOCARCINOGENICITY [J].
ELCOMBE, CR ;
ROSE, MS ;
PRATT, IS .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 1985, 79 (03) :365-376
[6]   BIOACTIVATION OF XENOBIOTICS BY FORMATION OF TOXIC GLUTATHIONE CONJUGATES [J].
KOOB, M ;
DEKANT, W .
CHEMICO-BIOLOGICAL INTERACTIONS, 1991, 77 (02) :107-136
[7]  
TANAKA S, 1968, BR J IND MED, V17, P60
[8]   GENOTOXICITY OF HALOALKENE AND HALOALKANE GLUTATHIONE S-CONJUGATES IN PORCINE KIDNEY-CELLS [J].
VAMVAKAS, S ;
DEKANT, W ;
HENSCHLER, D .
TOXICOLOGY IN VITRO, 1989, 3 (02) :151-156