Glutathione transferase activity and formation of macromolecular adducts in two cases of acute methyl bromide poisoning

被引:45
作者
Garnier, R
RambourgSchepens, MO
Muller, A
Hallier, E
机构
[1] HOP FERNAND WIDAL,INST INTERUNIV MED TRAVAIL,F-75010 PARIS,FRANCE
[2] HOP MAISON BLANCHE,CTR ANTIPOISONS,F-51092 REIMS,FRANCE
[3] UNIV DORTMUND,INST ARBEITSPHYSIOL,D-44139 DORTMUND,GERMANY
关键词
methyl bromide; poisoning; glutathione transferase;
D O I
10.1136/oem.53.3.211
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
Objectives-To determine the activity of glutathione transferase and to measure the S-methylcysteine adducts in blood proteins, after acute inhalational exposure to methyl bromide. To examine the influence of the polymorphism of glutathione-S-transferase theta (GSTT1) on the neurotoxicity of methyl bromide. Methods-Two workers acutely exposed to methyl bromide with inadequate respiratory protective devices were poisoned. Seven weeks after the accident, blood samples were drawn from both patients, for measurement of glutathione transferase activity in erythrocytes (conjugator status-that is, GSTT1 phenotype) and measurement of binding products of methyl bromide with blood proteins. Conjugator status was determined by a standard procedure. The binding product of methyl bromide, S-methylcysteine, was measured in globin and albumin. Results-Duration and intensity of exposure were identical for both patients as they worked together with the same protective devices and with similar physical effort. However, one patient had very severe poisoning, whereas the other only developed mild neurotoxic symptoms. The first patient was a ((conjugator)) with normal glutathione transferase activity, whereas this activity was undetectable in the erythrocytes of the second patient, who consequently had higher concentrations of S-methylcysteine adduct in albumin (149 v 91 nmol/g protein) and in globin (77 v 30 nmol/g protein). Conclusions-Methyl bromide is genotoxic and neurotoxic. Its genotoxicity seems to be the consequence of the alkylating activity of the parent compound, and conjugation to glutathione has a protective effect. The data presented here suggest a different mechanism for methyl bromide neurotoxicity which could be related to the transformation of methylglutathione into toxic metabolites such as methanethiol and formaldehyde. If such metabolites are the ultimate toxic species, N-acetylcysteine treatment could have a toxifying rather than a detoxifying effect.
引用
收藏
页码:211 / 215
页数:5
相关论文
共 32 条
[1]  
ALEXEEFF GV, 1983, RESIDUE REV, V88, P101
[2]   DETERMINATION OF ACUTE TOXIC EFFECTS IN MICE FOLLOWING EXPOSURE TO METHYL-BROMIDE [J].
ALEXEEFF, GV ;
KILGORE, WW ;
MUNOZ, P ;
WATT, D .
JOURNAL OF TOXICOLOGY AND ENVIRONMENTAL HEALTH, 1985, 15 (01) :109-123
[3]  
[Anonymous], ENV HLTH CRIT
[4]   BIOCHEMICAL STUDIES OF TOXIC AGENTS - METABOLISM OF IODOMETHANE [J].
BARNSLEY, EA ;
YOUNG, L .
BIOCHEMICAL JOURNAL, 1965, 95 (01) :77-&
[5]  
BLOM HJ, 1988, J LAB CLIN MED, V111, P606
[6]  
BONNEFOI MS, 1991, NEUROTOXICOLOGY, V12, P33
[7]   REGRESSION OF METHYL BROMIDE-INDUCED FORESTOMACH LESIONS IN THE RAT [J].
BOORMAN, GA ;
HONG, HL ;
JAMESON, CW ;
YOSHITOMI, K ;
MARONPOT, RR .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 1986, 86 (01) :131-139
[9]   INHIBITION OF THE ACUTE TOXICITY OF METHYL-CHLORIDE IN MALE B6C3F1 MICE BY GLUTATHIONE DEPLETION [J].
CHELLMAN, GJ ;
WHITE, RD ;
NORTON, RM ;
BUS, JS .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 1986, 86 (01) :93-104
[10]   METHYLBROMIDE - CARCINOGENIC EFFECTS IN THE RAT FORESTOMACH [J].
DANSE, LHJC ;
VANVELSEN, FL ;
VANDERHEIJDEN, CA .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 1984, 72 (02) :262-271