EC-SOD and the response to inflammatory reactions and aging in mouse lung

被引:11
作者
Sentman, ML [1 ]
Brännström, T [1 ]
Marklund, SL [1 ]
机构
[1] Univ Umea Hosp, Dept Med Biosci, SE-90185 Umea, Sweden
关键词
endotoxin; zymosan; oxidative stress; cytokines; bronchoalveolar lavage fluid; free radicals;
D O I
10.1016/S0891-5849(02)00790-6
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 lung is exposed to high oxygen tension and oxygen free radicals have been implicated in many pathologies of the organ. Extracellular superoxide dismutase occurs in high concentration in the lung and protects against hyperoxia-induced inflammation. We hypothesized that the enzyme might ameliorate other types of inflammation as well as aging-related changes of the organ. Tracheal instillation of endotoxin plus zymosan into extracellular superoxide dismutase knockout and wild-type mice resulted in a marked neutrophilic inflammation and increases in inflammatory cytokines, protein, and lactate dehydrogenase activity in the bronchoalveolar lavage fluid. There were no significant differences between the genotypes. Repeated challenges with ovalbumin caused an allergic inflammation with increases in eosinophils, interleukin-5, protein, and lactate dehydrogenase activity in the bronchoalveolar lavage fluid. Only minimal differences between the genotypes were found. In lungs from 2-year-old mice, marginal increases in inflammatory variables and fibrosis were found in the knockout mice. In conclusion, extracellular superoxide dismutase had a negligible role in the present inflammation and allergy models and for the long-term integrity of the organ. (C) 2002 Elsevier Science Inc.
引用
收藏
页码:975 / 981
页数:7
相关论文
共 45 条
[1]   Lipopolysaccharide-induced lung injury in mice. I. Concomitant evaluation of inflammatory cells and haemorrhagic lung damage [J].
Asti, C ;
Ruggieri, V ;
Porzio, S ;
Chiusaroli, R ;
Melillo, G ;
Caselli, GF .
PULMONARY PHARMACOLOGY & THERAPEUTICS, 2000, 13 (02) :61-69
[2]   MITIGATION OF OXIDANT INJURY TO LUNG MICROVASCULATURE BY INTRATRACHEAL INSTILLATION OF ANTIOXIDANT ENZYMES [J].
BARNARD, ML ;
BAKER, RR ;
MATALON, S .
AMERICAN JOURNAL OF PHYSIOLOGY, 1993, 265 (04) :L340-L345
[3]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[4]   MICE LACKING EXTRACELLULAR-SUPEROXIDE DISMUTASE ARE MORE SENSITIVE TO HYPEROXIA [J].
CARLSSON, LM ;
JONSSON, J ;
EDLUND, T ;
MARKLUND, SL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (14) :6264-6268
[5]   Rapid loss of superoxide dismutase activity during antigen-induced asthmatic response [J].
Comhair, SAA ;
Bhathena, PR ;
Dweik, RA ;
Kavuru, M ;
Erzurum, SC .
LANCET, 2000, 355 (9204) :624-624
[6]   Oxidant stress in asthma [J].
Dworski, R .
THORAX, 2000, 55 :S51-S53
[7]   Effects of same anti-asthma drugs on human eosinophil superoxide anions release and degranulation [J].
Ezeamuzie, CI ;
Al-Hage, M .
INTERNATIONAL ARCHIVES OF ALLERGY AND IMMUNOLOGY, 1998, 115 (02) :162-168
[8]   Oxidants, oxidative stress and the biology of ageing [J].
Finkel, T ;
Holbrook, NJ .
NATURE, 2000, 408 (6809) :239-247
[9]   Extracellular superoxide dismutase in the airways of transgenic mice reduces inflammation and attenuates lung toxicity following hyperoxia [J].
Folz, RJ ;
Abushamaa, AM ;
Suliman, HB .
JOURNAL OF CLINICAL INVESTIGATION, 1999, 103 (07) :1055-1066
[10]   Increased nitrotyrosine in exhaled breath condensate of patients with asthma [J].
Hanazawa, T ;
Kharitonov, SA ;
Barnes, PJ .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2000, 162 (04) :1273-1276