NUTRIM School for Nutrition, Toxicology and Metabolism, Department of Respiratory Medicine, Maastricht University Medical Centre+ (MUMC+), Maastricht, The Netherlands.
Health Risk Analysis and Toxicology, Maastricht University Medical Centre+ (MUMC+), Maastricht, The Netherlands.
Chest. 2011 Feb;139(2):337-346. doi: 10.1378/chest.10-0275. Epub 2010 Aug 5.
Nuclear factor (NF)-κB activation and oxidative stress are physiologic responses of skeletal muscle to exercise but may be impaired in patients with COPD. Therefore, we investigated NF-κB activity and expression of NF-κB-regulated genes in muscle of patients with COPD and control subjects before and after exercise.
Quadriceps specimens were obtained before, immediately after, and 2 h after a submaximal cycle ergometry test from seven patients with COPD (50.6 ± 5.7 SEM FEV(1) of patients with COPD) and seven age-matched control subjects. NF-κB DNA-binding activity in muscle and peripheral blood mononuclear cells (PBMCs) was determined using electrophoretic mobility shift assay and enzyme-linked immunosorbent assay, respectively. mRNA expression and protein carbonylation were measured by real-time polymerase chain reaction and Western blot, respectively.
In control subjects, IL-6, IκBα, tumor necrosis factor-α, IL-1β, superoxide dismutase, thioredoxin, heme oxygenase 1, and heat shock protein-70 were upregulated in muscle after exercise, whereas in patients with COPD only IL-6 mRNA was increased. Exercise-induced antiapoptotic Bcl2 mRNA levels were attenuated in patients with COPD compared with control subjects. Basal muscle protein oxidation was higher in patients with COPD than in control subjects, but attenuated in response to exercise. No exercise-induced changes in NF-κB DNA-binding activity in muscle and PBMCs of either group were detected.
Skeletal muscle of patients with COPD is characterized by an impaired response to exercise of NF-κB-regulated genes encoding inflammatory cytokines, antioxidants, stress proteins, and survival factors.
核因子(NF)-κB 的激活和氧化应激是骨骼肌对运动的生理反应,但在 COPD 患者中可能受损。因此,我们研究了 COPD 患者和对照受试者运动前后肌肉中 NF-κB 的活性和 NF-κB 调节基因的表达。
从 7 名 COPD 患者(FEV1 为患者的 50.6±5.7 SEM)和 7 名年龄匹配的对照受试者中,在亚最大循环测功仪测试前、后立即和 2 小时后获得股四头肌标本。使用电泳迁移率变动分析和酶联免疫吸附试验分别测定肌肉和外周血单核细胞(PBMC)中的 NF-κB DNA 结合活性。通过实时聚合酶链反应和 Western blot 分别测量 mRNA 表达和蛋白羰基化。
在对照受试者中,运动后肌肉中 IL-6、IκBα、肿瘤坏死因子-α、IL-1β、超氧化物歧化酶、硫氧还蛋白、血红素加氧酶 1 和热休克蛋白 70 上调,而在 COPD 患者中仅 IL-6 mRNA 增加。与对照受试者相比,运动诱导的抗凋亡 Bcl2 mRNA 水平在 COPD 患者中减弱。与对照受试者相比,COPD 患者的肌肉基础蛋白氧化水平较高,但运动后减弱。两组肌肉和 PBMC 中均未检测到 NF-κB DNA 结合活性的运动诱导变化。
COPD 患者的骨骼肌对运动的 NF-κB 调节基因编码的炎症细胞因子、抗氧化剂、应激蛋白和生存因子的反应受损。