دورية أكاديمية

Protective effects of fomepizole on 2-chloroethanol toxicity.

التفاصيل البيبلوغرافية
العنوان: Protective effects of fomepizole on 2-chloroethanol toxicity.
المؤلفون: Yng-Tay Chen, Jiunn-Wang Liao, Dong-Zong Hung
المصدر: Human & Experimental Toxicology; Jun2010, Vol. 29 Issue 6, p507-512, 6p, 2 Charts, 2 Graphs
مصطلحات موضوعية: TOXICITY testing, FOOD poisoning, ANTIDOTES, ALDEHYDES, DEHYDROGENASES, LABORATORY rats
مستخلص: 2-Chloroethanol (2-CE) is a widely used industrial solvent. In Taiwan, Taiwanese farmers apply 2-CE on grapevines to accelerate grape growth, a practice that in some cases have caused poisoning in humans. Thus, there is strong interest in identifying antidotes to 2-CE. This study examines the protective role in 2-CE intoxicated rats. Alcohol dehydrogenase and glutathione were hypothesized to be important in the metabolism of 2-CE. This study used fomepizole, an alcohol dehydrogenase inhibitor, and chemicals that affected glutathione metabolism to study 2-CE toxicity. Notably, fomepizole 5 mg/kg significantly increased median lethal dose (LD50) of 2-CE from 65.1 to 180 mg/kg and reduced the production of a potential toxic metabolite chloroacetaldehyde (CAA) in animal plasma. In contrast, disulfiram (DSF), an aldehyde dehydrogenase inhibitor, increased the toxicity of 2-CE on the lethality in rats. Additional or pretreatment with N-acetylcysteine (NAC) and fomepizole significantly reduced plasma CAA concentrations. Fomepizole also significantly reduced 2-CEinhibited glutathione activity. Otherwise, pretreatment with NAC for 4 days followed by co-treatment with fomepizole significantly decreased formation of the metabolic CAA. These results indicated that its catalytic enzyme might play a vital role during 2-CE intoxication, and the combination of fomepizole and NAC could be a protective role in cases of acute 2-CE intoxication. [ABSTRACT FROM AUTHOR]
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قاعدة البيانات: Complementary Index
الوصف
تدمد:09603271
DOI:10.1177/0960327109358612