Effects of aminoguanidine and antioxidant erdosteine on bleomycin-induced lung fibrosis in rats

被引:54
作者
Yildirim, Z [1 ]
Turkoz, Y
Kotuk, M
Armutcu, F
Gurel, A
Iraz, M
Ozen, S
Aydogdu, I
Akyol, O
机构
[1] Inonu Univ, Fac Med, Dept Pulm Med, TR-44069 Malatya, Turkey
[2] Inonu Univ, Fac Med, Dept Biochem, TR-44069 Malatya, Turkey
[3] Karaelmas Univ, Fac Med, Dept Biochem, Zonguldak, Turkey
[4] Inonu Univ, Fac Med, Dept Pharmacol, Malatya, Turkey
[5] Yuzuncuyil Univ, Fac Med, Dept Pathol, Van, Turkey
[6] Inonu Univ, Fac Med, Dept Hematol, Malatya, Turkey
来源
NITRIC OXIDE-BIOLOGY AND CHEMISTRY | 2004年 / 11卷 / 02期
关键词
bleomycin; lung fibrosis; nitric oxide; aminoguanidin; erdosteine;
D O I
10.1016/j.niox.2004.07.011
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
Reactive oxygen and nitrogen species have been implicated in the pathogenesis of bleomycin -induced lung fibrosis. The effects of aminoguanidine and erdosteine on the bleomycin-induced lung fibrosis were evaluated in rats. The animals were placed into five groups: Vehicle + vehicle, vehicle + bleomycin (2.5U/kg), bleomycin + aminoguanidine (200mg/kg), bleomycin + erdosteine (10mg/kg), and bleomycin + erdosteine + aminoguanidine. Bleomycin administration resulted in prominent lung fibrosis as measured by lung hydroxyproline content and lung histology, which is completely prevented by erdosteine and aminoguanidine. A strong staining for nitro tyrosine antibody in lung tissue and increased levels of lung NO were found in bleomycin group, that were significantly reduced by aminoguanidine and erdosteine. Aminoguanidine and erdosteine significantly prevented depletion of superoxide dismutase and glutathione peroxidase and elevated myeloperoxidase activities, malondialdehyde level in lung tissue produced by bleomycin. Data presented here indicate that aminoguanidine and erdosteine prevented bleomycin-induced lung fibrosis and that nitric oxide mediated tyrosine nitration of proteins plays a significant role in the pathogenesis of bleomycin-induced lung fibrosis. Also our data suggest that antifibrotic affect of antioxidants may be due to their inhibitory effect on nitric oxide generation in this model. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:156 / 165
页数:10
相关论文
共 40 条
[1]  
[Anonymous], [No title captured]
[2]   SIMPLE METHOD OF ESTIMATING SEVERITY OF PULMONARY FIBROSIS ON A NUMERICAL SCALE [J].
ASHCROFT, T ;
SIMPSON, JM ;
TIMBRELL, V .
JOURNAL OF CLINICAL PATHOLOGY, 1988, 41 (04) :467-470
[3]   Oxidative damage and tyrosine nitration from peroxynitrite [J].
Beckman, JS .
CHEMICAL RESEARCH IN TOXICOLOGY, 1996, 9 (05) :836-844
[4]   EFFECT OF DEOXYRIBONUCLEIC-ACID ON THE PRODUCTION OF REDUCED OXYGEN BY BLEOMYCIN AND IRON [J].
CASPARY, WJ ;
LANZO, DA ;
NIZIAK, C .
BIOCHEMISTRY, 1982, 21 (02) :334-338
[5]  
Chen XL, 2003, ACTA PHARMACOL SIN, V24, P697
[6]  
Chen XL, 2001, ACTA PHARMACOL SIN, V22, P711
[7]  
CORTAS NK, 1990, CLIN CHEM, V36, P1440
[8]   ANTIOXIDANT THERAPY PARTIALLY BLOCKS IMMUNE-INDUCED LUNG FIBROSIS [J].
DENIS, M .
INFLAMMATION, 1995, 19 (02) :207-219
[9]   Dual role of inducible nitric oxide synthase in acute asbestos-induced lung injury [J].
Dörger, M ;
Allmeling, AM ;
Kiefmann, R ;
Schropp, A ;
Krombach, F .
FREE RADICAL BIOLOGY AND MEDICINE, 2002, 33 (04) :491-501
[10]   Formation of nitric oxide derived inflammatory oxidants by myeloperoxidase in neutrophils [J].
Eiserich, JP ;
Hristova, M ;
Cross, CE ;
Jones, AD ;
Freeman, BA ;
Halliwell, B ;
van der Vliet, A .
NATURE, 1998, 391 (6665) :393-397