Effects of N-acetyl-L-cysteine and glutathione on antioxidant status of human serum and 3T3 fibroblasts

被引:14
作者
Hong, SY
Yang, JO
Lee, EY
Lee, ZW
机构
[1] Soonchunhyang Univ, Cheonan Hosp, Dept Internal Med, Cheonan 330100, South Korea
[2] Soonchunhyang Univ, Cheonan Hosp, Clin Res Inst, Cheonan 330100, South Korea
[3] Korea Basic Sci Inst, Cell Biol Team, Taejon, South Korea
关键词
antioxidants; glutathione; acetylcysteine; paraquat; poisoning;
D O I
10.3346/jkms.2003.18.5.649
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The effectiveness of several sulfhydryl compounds in the treatment of paraquat intoxication has been previously tested based on their antioxidant ability. However, practical guidelines for their clinical use remain to be determined. As a preliminary pharmacokinetic study on sulfhydryl compounds, we attempted to establish the optimal concentration of N-acetyl-L-cysteine, glutathione, superoxide dismutase, and catalase. We measured the antioxidant effect of these antioxidants in normal pooled plasma and on intracellular reactive oxygen species (ROS) induced by paraquat. N-acetyl-L-cysteine begins to suppress the production of ROS in plasma at concentrations as low as 5 mM, with the suppression being maximal at 40 mM. In the same way, glutathione increased the total antioxidant status in plasma at concentrations of 5-40 mM in a dose-dependent manner. Complete suppression of ROS in plasma induced by exposure to 500 muM paraquat for 40 min was observed when using 40 mM N-acetyl-L-cysteine and 5 mM glutathione. These concentrations are comparable with 50 units of catalase, which reduced ROS at concentrations of 5-100 units. Further pharmacokinetic study into the systemic administration of these antioxidants is necessary, using effective concentrations of 5-40 mM for both N-acetyl-L-cysteine and glutathione, and 1-50 units of catalase.
引用
收藏
页码:649 / 654
页数:6
相关论文
共 29 条
[1]   DETERMINATION OF PARAQUAT (1,1'-DIMETHYL-4,4'-BIPYRIDYLIUM CATION) IN URINE [J].
BERRY, DJ ;
GROVE, J .
CLINICA CHIMICA ACTA, 1971, 34 (01) :5-&
[2]   GLUTATHIONE PROTECTION IN ALVEOLAR TYPE-II CELLS FROM FETAL AND NEONATAL RABBITS [J].
BROWN, LAS ;
BAI, CL ;
JONES, DP .
AMERICAN JOURNAL OF PHYSIOLOGY, 1992, 262 (03) :L305-L312
[3]   MECHANISM OF PARAQUAT TOXICITY IN MICE AND RATS [J].
BUS, JS ;
CAGEN, SZ ;
OLGAARD, M ;
GIBSON, JE .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 1976, 35 (03) :501-513
[4]   Cellular glutathione peroxidase is the mediator of body selenium to protect against paraquat lethality in transgenic mice [J].
Cheng, WH ;
Ho, YS ;
Valentine, BA ;
Ross, DA ;
Combs, GF ;
Lei, XG .
JOURNAL OF NUTRITION, 1998, 128 (07) :1070-1076
[5]  
Domenighetti G, 1999, REV MAL RESPIR, V16, P29
[6]   Determination of activity of antioxidants in human subjects [J].
Duthie, GG .
PROCEEDINGS OF THE NUTRITION SOCIETY, 1999, 58 (04) :1015-1024
[7]   GLUTATHIONE - INTERORGAN TRANSLOCATION, TURNOVER, AND METABOLISM [J].
GRIFFITH, OW ;
MEISTER, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1979, 76 (11) :5606-5610
[8]   PROTECTION AGAINST PARAQUAT-INDUCED INJURY BY EXOGENOUS GSH IN PULMONARY ALVEOLAR TYPE-II CELLS [J].
HAGEN, TM ;
BROWN, LA ;
JONES, DP .
BIOCHEMICAL PHARMACOLOGY, 1986, 35 (24) :4537-4542
[9]   N-acetylcysteine increases the glutathione content and protects rat alveolar type II cells against paraquat-induced cytotoxicity [J].
Hoffer, E ;
Baum, Y ;
Tabak, A ;
Taitelman, U .
TOXICOLOGY LETTERS, 1996, 84 (01) :7-12
[10]   Associations between laboratory parameters and outcome of paraquat poisoning [J].
Hong, SY ;
Yang, DH ;
Hwang, KY .
TOXICOLOGY LETTERS, 2000, 118 (1-2) :53-59