In vivo protection of a water-soluble derivative of vitamin E, Trolox, against methylmercury-intoxication in the rat

被引:80
作者
Usuki, F
Yasutake, A
Umehara, F
Tokunaga, H
Matsumoto, M
Eto, K
Ishiura, S
Higuchi, I
机构
[1] Natl Inst Minamata Dis, Dept Clin Med, Minamata 8670008, Japan
[2] Natl Inst Minamata Dis, Biochem Sect, Minamata 8670008, Japan
[3] Kagoshima Univ, Sch Med, Dept Internal Med 3, Kagoshima 890, Japan
[4] Kumamoto Univ, Sch Med, Dept Surg Pathol, Kumamoto 8608555, Japan
[5] Univ Tokyo, Grad Sch Arts & Sci, Dept Life Sci, Meguro Ku, Tokyo 153, Japan
关键词
methylmercury-intoxication; mitochondrial electron transport system; apoptosis; oxidative stress; antioxidant; trolox (6-hydroxy-2,5,7,8-tetramethylchroman-2-carboxylic acid); in vivo protection;
D O I
10.1016/S0304-3940(01)01764-5
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Methylmercury (MeHg) is a well-known neurotoxicant. MeHg-intoxication causes a disturbance in mitochondrial energy metabolism in skeletal muscle and apoptosis in cerebellum. We report the first in vivo effectiveness of antioxidant Trolox (6-hydroxy-2,5,7,8-tetramethylchroman-2-carboxylic acid), a water soluble vitamin E analog, against the MeHg-induced cellular responses. Treatment with Trolox (6-hydroxy-2.5,7,8-tetramethylchroman-2-carboxylic acid) clearly protects MeHg-treated rat skeletal muscle against the decrease in mitochondrial electron transport system enzyme activities despite the retention of MeHg. Tdt-mediated dUTP nick-end-labeling method clarified that Trolox is effective for protecting cerebellum from MeHg-induced apoptosis. These data indicate that MeHg-mediated oxidative stress plays an important role in the in vivo pathological process of MeHg intoxication. Trolox may prevent some of clinical manifestations of MeHg-intoxication in humans. (C) 2001 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:199 / 203
页数:5
相关论文
共 19 条
[1]   UPTAKE OF METHYLMERCURY IN THE RAT-BRAIN - EFFECTS OF AMINO-ACIDS [J].
ASCHNER, M ;
CLARKSON, TW .
BRAIN RESEARCH, 1988, 462 (01) :31-39
[3]   Cognitive deficit in 7-year-old children with prenatal exposure to methylmercury [J].
Grandjean, P ;
Weihe, P ;
White, RF ;
Debes, F ;
Araki, S ;
Yokoyama, K ;
Murata, K ;
Sorensen, N ;
Dahl, R ;
Jorgensen, PJ .
NEUROTOXICOLOGY AND TERATOLOGY, 1997, 19 (06) :417-428
[4]   Mitochondria and apoptosis [J].
Green, DR ;
Reed, JC .
SCIENCE, 1998, 281 (5381) :1309-1312
[5]  
Hamada R., 1996, TOXICOLOGY METALS, P337
[6]  
Harada M, 1997, MINERAL METAL NEUROT, P177
[8]   ARC, an inhibitor of apoptosis expressed in skeletal muscle and heart that interacts selectively with caspases [J].
Koseki, T ;
Inohara, N ;
Chen, S ;
Nunez, G .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (09) :5156-5160
[9]   GLUTATHIONE PEROXIDASE-ACTIVITY IN SELENIUM-DEFICIENT RAT-LIVER [J].
LAWRENCE, RA ;
BURK, RF .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1976, 71 (04) :952-958
[10]  
LOWRY OH, 1951, J BIOL CHEM, V193, P265