Xanthine oxidase inhibition reduces reactive nitrogen species production in COPD airways

被引:39
作者
Ichinose, M [1 ]
Sugiura, H
Yamagata, S
Koarai, A
Tomaki, M
Ogawa, H
Komaki, Y
Barness, PJ
Shirato, K
Hattori, T
机构
[1] Wakayama Med Univ, Dept Internal Med 3, Wakayama 8111, Japan
[2] Tohoku Univ, Grad Sch Med, Div Resp & Infect Dis, Sendai, Miyagi 980, Japan
[3] Univ London Imperial Coll Sci & Technol, Natl Heart & Lung Inst, Dept Thorac Med, London, England
关键词
chronic obstructive pulmonary disease; exhaled nitric oxide; nitrotvrosine;
D O I
10.1183/09031936.03.00052002
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Reactive nitrogen species (RNS) have been reported to be involved in the inflammatory process in chronic obstructive pulmonary disease (COPD). However, there are no studies on the modulation of RNS in COPD. It was hypothesised that inhibition of xanthine oxidase (XO) might decrease RNS production in COPD airways through the suppression of superoxide anion production. Ten COPD and six healthy subjects participated in the study. The XO inhibitor allopurinol (300 mg.day(-1) p.o. for 4 weeks) was administered to COPD patients. RNS production in the airway was assessed by 3-nitrotyrosine immunoreactivity and enzymic activity of XO in induced sputum as well as by exhaled nitric oxide (eNO) concentration. XO activity in the airway was significantly elevated in COPD compared with healthy subjects. Allopurinol administration to COPD subjects significantly decreased XO activity and nitrotyrosine formation. In contrast, eNO concentration was significantly increased by allopurinol administration. These results suggest that oral administration of the xanthine oxidase inhibitor allopurinol reduces airway reactive nitrogen species production in chronic obstructive pulmonary disease subjects. This intervention may be useful in the future management of chronic obstructive pulmonary disease.
引用
收藏
页码:457 / 461
页数:5
相关论文
共 29 条
  • [1] DEPENDENCE ON O-2- GENERATION BY XANTHINE-OXIDASE OF PATHOGENESIS OF INFLUENZA-VIRUS INFECTION IN MICE
    AKAIKE, T
    ANDO, M
    ODI, T
    DOI, T
    IJIRI, S
    ARAKI, S
    MAEDA, H
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1990, 85 (03) : 739 - 745
  • [2] [Anonymous], 1987, AM REV RESPIR DIS, V136, P225
  • [3] Medical progress: Chronic obstructive pulmonary disease.
    Barnes, PJ
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2000, 343 (04) : 269 - 280
  • [4] New therapies for chronic obstructive pulmonary disease
    Barnes, PJ
    [J]. THORAX, 1998, 53 (02) : 137 - 147
  • [5] APPARENT HYDROXYL RADICAL PRODUCTION BY PEROXYNITRITE - IMPLICATIONS FOR ENDOTHELIAL INJURY FROM NITRIC-OXIDE AND SUPEROXIDE
    BECKMAN, JS
    BECKMAN, TW
    CHEN, J
    MARSHALL, PA
    FREEMAN, BA
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (04) : 1620 - 1624
  • [6] Oxidative damage and tyrosine nitration from peroxynitrite
    Beckman, JS
    [J]. CHEMICAL RESEARCH IN TOXICOLOGY, 1996, 9 (05) : 836 - 844
  • [7] Beckman JS, 1996, AM J PHYSIOL-CELL PH, V271, pC1424
  • [8] KINETICS OF SUPEROXIDE DISMUTASE-CATALYZED AND IRON-CATALYZED NITRATION OF PHENOLICS BY PEROXYNITRITE
    BECKMAN, JS
    ISCHIROPOULOS, H
    ZHU, L
    VANDERWOERD, M
    SMITH, C
    CHEN, J
    HARRISON, J
    MARTIN, JC
    TSAI, M
    [J]. ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1992, 298 (02) : 438 - 445
  • [9] Formation of nitric oxide derived inflammatory oxidants by myeloperoxidase in neutrophils
    Eiserich, JP
    Hristova, M
    Cross, CE
    Jones, AD
    Freeman, BA
    Halliwell, B
    van der Vliet, A
    [J]. NATURE, 1998, 391 (6665) : 393 - 397
  • [10] Xanthine oxidase is involved in exercise-induced oxidative stress in chronic obstructive pulmonary disease
    Heunks, LMA
    Viña, J
    Van Herwaarden, CLA
    Folgering, HTM
    Gimeno, A
    Dekhuijzen, PNR
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY-REGULATORY INTEGRATIVE AND COMPARATIVE PHYSIOLOGY, 1999, 277 (06) : R1697 - R1704