Suppression of type II collagen-induced arthritis by N-acetyl-L-cysteine in mice

被引:23
作者
Kroger, H
Miesel, R
Dietrich, A
Ohde, M
Altrichter, S
Braun, C
Ockenfels, H
机构
[1] UNIV OTAGO, DEPT BIOCHEM, DUNEDIN, NEW ZEALAND
[2] UNIV ULM, DEPT PHYSIOL CHEM, ULM, GERMANY
来源
GENERAL PHARMACOLOGY-THE VASCULAR SYSTEM | 1997年 / 29卷 / 04期
关键词
N-acetyl-L-cysteine; collagen-induced arthritis; oxidative stress; reactive oxygen species;
D O I
10.1016/S0306-3623(96)00570-8
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
1. The antiarthritic and anti-inflammatory efficacy of N-acetyl-L-cysteine (NAC) was tested in male DBA/1 hybrid mice suffering from type II collagen-induced arthritis. Parameters including the arthritis index and the phagocytic responses recorded by chemiluminescence in unseparated blood were used for the assessment of disease activity. 2. Mice were immunized by subdermal injection of bovine type II collagen in Freund's complete adjuvant. The treatment with NAC started at day 42 after immunization and was continued over a period of six weeks: in doses ranging up to 50 mg/kg, a dose dependent suppression of arthritis was noted; between 50 and 200 mg/kg, the inhibition curve had a plateau [ED50=50 mg/(kg x day)]. 3. The arthritis index correlated positively with the generation of chemiluminescence by reactive oxygen species (ROS) produced in neutrophils and monocytes activated by 12-O-tetradecanoylphorbol 13-acetate. 4. After treatment with 100 mg/kg of NAC from day 42 after immunization over a period of six weeks, the ROS production was reduced to levels occurring. in whole blood of healthy animals. 5. It is concluded that low molecular-weight antioxidants such as NAC may be adequate for controlling oxidative stress-derived damage in rheumatic diseases by modulation of ROS dependent signal transduction pathways. (C) 1997 Elsevier Science Inc.
引用
收藏
页码:671 / 674
页数:4
相关论文
共 24 条
[1]  
[Anonymous], 1991, OXIDATIVE STRESS OXI
[2]   PARTICULATE SUPEROXIDE-FORMING SYSTEM FROM HUMAN NEUTROPHILS - PROPERTIES OF SYSTEM AND FURTHER EVIDENCE SUPPORTING ITS PARTICIPATION IN RESPIRATORY BURST [J].
BABIOR, BM ;
CURNUTTE, JT ;
MCMURRICH, BJ .
JOURNAL OF CLINICAL INVESTIGATION, 1976, 58 (04) :989-996
[3]  
BEUTLER B, 1989, ANNU REV IMMUNOL, V7, P625, DOI 10.1146/annurev.iy.07.040189.003205
[4]   ARTHRITOGENICITY OF MINOR CARTILAGE COLLAGENS (TYPE-IX AND TYPE-XI) IN MICE [J].
BOISSIER, MC ;
CHIOCCHIA, G ;
RONZIERE, MC ;
HERBAGE, D ;
FOURNIER, C .
ARTHRITIS AND RHEUMATISM, 1990, 33 (01) :1-8
[5]   PRIMED LYMPHOCYTES ARE BOOSTED BY TYPE-II COLLAGEN OF THEIR HOSTS AFTER ADOPTIVE TRANSFER [J].
DIETRICH, A ;
MITCHISON, NA ;
RAJNAVOLGYI, E ;
SCHNEIDER, SC .
JOURNAL OF AUTOIMMUNITY, 1994, 7 (05) :601-609
[6]  
FONG KY, 1994, CLIN EXP RHEUMATOL, V12, P55
[7]   N-ACETYLCYSTEINE AMELIORATES REPERFUSION INJURY AFTER WARM HEPATIC ISCHEMIA [J].
FUKUZAWA, K ;
EMRE, S ;
SENYUZ, O ;
ACARLI, K ;
SCHWARTZ, ME ;
MILLER, CM .
TRANSPLANTATION, 1995, 59 (01) :6-9
[8]   COPPER DEPENDENT CONTROL OF THE ENZYMIC AND PHAGOCYTE INDUCED DEGRADATION OF SOME BIO-POLYMERS, A POSSIBLE LINK TO SYSTEMIC INFLAMMATION [J].
HARTMANN, HJ ;
GARTNER, A ;
WESER, U .
CLINICA CHIMICA ACTA, 1985, 152 (1-2) :95-103
[9]   Synergistic effects of thalidomide and poly(ADP-ribose) polymerase inhibition on type II collagen-induced arthritis in mice [J].
Kroger, H ;
Miesel, R ;
Dietrich, A ;
Ohde, M ;
Rajnavolgyi, E ;
Ockenfels, H .
INFLAMMATION, 1996, 20 (02) :203-215
[10]   NF-KAPPA-B - A PLEIOTROPIC MEDIATOR OF INDUCIBLE AND TISSUE-SPECIFIC GENE-CONTROL [J].
LENARDO, MJ ;
BALTIMORE, D .
CELL, 1989, 58 (02) :227-229