Oxidative stress and respiratory muscle dysfunction in severe chronic obstructive pulmonary disease

被引:165
|
作者
Barreiro, E
de la Puente, B
Minguella, J
Corominas, JM
Serrano, S
Hussain, SNA
Gea, L
机构
[1] Univ Pompeu Fabra, Muscle Res & Resp Syst Unit, Dept Resp Med, IMIM,Hosp Mar, Barcelona, Spain
[2] Univ Pompeu Fabra, Muscle Res & Resp Syst Unit, Dept Surg, IMIM,Hosp Mar, Barcelona, Spain
[3] Univ Pompeu Fabra, Muscle Res & Resp Syst Unit, Dept Pathol, IMIM,Hosp Mar, Barcelona, Spain
[4] Univ Autonoma Barcelona, E-08193 Barcelona, Spain
[5] Royal Victoria Hosp, Crit Care Div, Montreal, PQ H3A 1A1, Canada
[6] Royal Victoria Hosp, Div Resp, Montreal, PQ H3A 1A1, Canada
[7] McGill Univ, Meakins Christie Labs, Montreal, PQ, Canada
关键词
chronic obstructive pulmonary disease; diaphragm strength; oxidative stress;
D O I
10.1164/rccm.200407-887OC
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Rationale: Oxidative stress is involved in the skeletal muscle dysfunction observed in patients with severe chronic obstructive pulmonary disease (COPD). We hypothesized that the diaphragms of such patients might generate greater levels of oxidants than those neutralized by antioxidants. Objectives: To assess the levels of both oxidative and nitrosative stress and different antioxidants in the diaphragms of those patients, and to analyze potential relationships with lung and respiratory muscle dysfunctions. Methods and Measurements: We conducted a case-control study in which reactive carbonyl groups, hydroxynonenal-protein adducts, antioxidant enzyme levels, nitric oxide synthases, and 3-nitrotyrosine formation were detected using immunoblotting and immunhistochemistry in diaphragm specimens (thoracotomy) obtained from six patients with severe COPD, six patients with moderate COPD, and seven control subjects. Main Results: Diaphragms of patients with severe COPD showed both higher protein carbonyl groups and hydroxynonenalprotein adducts than control subjects. When only considering patients with COPD, negative correlations were found between carbonyl groups and airway obstruction, and between hydroxynonenal-protein adducts and respiratory muscle strength. Although diaphragmatic neuronal nitric oxide synthase did not differ among the three groups and no inducible nitric oxide synthase was detected in any muscle, muscle endothelial nitric oxide synthase was lower in patients with severe COPD than in control subjects. Muscle nitrotyrosine levels were similar in both patients with severe COPD and control subjects. Conclusions: This study shows that oxidative stress rather than nitric oxide is likely to be involved in the respiratory muscle dysfunction in severe COPD.
引用
收藏
页码:1116 / 1124
页数:9
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