Effect of 4-chloro-2-methylphenoxyacetic acid and 2,4-dimethylphenol on human erythrocytes

被引:18
作者
Bukowska, B [1 ]
Goszczynska, K [1 ]
Duda, W [1 ]
机构
[1] Univ Lodz, Dept Biophys Environm Pollut, PL-90237 Lodz, Poland
关键词
erythrocytes; glutathione; MCPA; 2,4-dimethylphenol; phenols; hemoglobin; AEC; ADP; ATP; AMP;
D O I
10.1016/j.pestbp.2003.08.006
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The effects of exposure of human erythrocytes to different concentrations of 4-chloro-2-methylphenoxyacetic acid (MCPA) and its metabolite-2,4-dimethylphenol (2,4-DMP) were studied. The investigations concerned mainly the content of glutathione (GSH and GSSG), glutathione peroxidase (GSH-Px), glutathione transferase (GST), and the level of adenine energy charge (AEC). Reactive oxygen species (ROS) such as hydroxyl radical, superoxide anion, hydrogen peroxide, and nitric oxide are produced during normal processes in the cell. Under normal conditions, antioxidant systems of the cell minimize damage caused by ROS. When ROS generation increases to an extent that it overcomes the cellular antioxidant systems, the result is oxidative stress. We observed that MCPA and 2,4-DMP decreased the level of GSH in erythrocytes in comparison with control. MCPA did not affect glutathione peroxidase and glutathione transferase activity, while 2,4-DMP increased their activity. 2,4-DMP decreased the level of ATP and increased the content of ADP and AMP, leading to the fall of the level of AEC. MCPA and 2,4-DMP transform hemoglobin into methemoglobin, thus preventing oxygen transport. Comparison of the toxicity of MCPA and 2,4-DMP revealed that the most prominent changes occurred in human erythrocytes incubated with 2,4-DMP. (C) 2003 Elsevier Inc. All rights reserved.
引用
收藏
页码:92 / 98
页数:7
相关论文
共 25 条
[11]  
Juteau P, 1995, APPL MICROBIOL BIOT, V44, P218, DOI 10.1007/BF00164505
[12]   Interferon/antioxidant combination therapy for chronic hepatitis C - a controlled pilot trial [J].
Look, MP ;
Gerard, A ;
Rao, GS ;
Sudhop, T ;
Fischer, HP ;
Sauerbruch, T ;
Spengler, U .
ANTIVIRAL RESEARCH, 1999, 43 (02) :113-122
[13]   Effects of antioxidant enzymes in the molecular control of reactive oxygen species toxicology [J].
Matés, JM .
TOXICOLOGY, 2000, 153 (1-3) :83-104
[14]  
MCBRAIN M, 1996, S AFR J SCI, V92, P426
[15]  
MILLS GC, 1961, J LAB CLIN MED, V58, P725
[16]   Coordinated action of glutathione S-Transferases (GSTs) and multidrug resistance protein 1 (MRP1) in antineoplastic drug detoxification -: Mechanism of GST A1-1- and MRP1-associated resistance to chlorambucil in MCF7 breast carcinoma cells [J].
Morrow, CS ;
Smitherman, PK ;
Diah, K ;
Schneider, E ;
Townsend, AJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (32) :20114-20120
[17]   QUINOL SULFATE, A NEW CONJUGATE OF PHENOL IN GOLDFISH [J].
NAGEL, R ;
URICH, K .
XENOBIOTICA, 1983, 13 (02) :97-100
[18]   Role of glutathione in stabilization of nitric oxide during hypertension developed by inhibition of nitric oxide synthase in the rat [J].
Pechánová, O ;
Kashiba, M ;
Inoue, M .
JAPANESE JOURNAL OF PHARMACOLOGY, 1999, 81 (02) :223-229
[19]  
Rice-Evans CA., 1991, TECHNIQUES FREE RADI
[20]   The effects of ethanol, hexan-1-ol, and 2-phenylethanol on cider yeast growth, viability, and energy status; Synergistic inhibition [J].
Seward, R ;
Willets, JC ;
Dinsdale, MG ;
Lloyd, D .
JOURNAL OF THE INSTITUTE OF BREWING, 1996, 102 (06) :439-443