Comhair Suzy A A, Ricci Kristin S, Arroliga Mercedes, Lara Abigail R, Dweik Raed A, Song Wei, Hazen Stanley L, Bleecker Eugene R, Busse William W, Chung Kian Fan, Gaston Benjamin, Hastie Annette, Hew Mark, Jarjour Nizar, Moore Wendy, Peters Stephen, Teague W Gerald, Wenzel Sally E, Erzurum Serpil C
Department of Pathology, Cleveland Clinic Foundation, OH 44195, USA.
Am J Respir Crit Care Med. 2005 Aug 1;172(3):306-13. doi: 10.1164/rccm.200502-180OC. Epub 2005 May 5.
Increased oxidative stress and decreased superoxide dismutase (SOD) activity in the asthmatic airway are correlated to airflow limitation and hyperreactivity. We hypothesized that asthmatic individuals with higher levels of oxidative stress may have greater loss of SOD activity, which would be reflected systemically in loss of circulating SOD activity and clinically by development of severe asthma and/or worsening airflow limitation.
To investigate this, serum SOD activity and proteins, the glutathione peroxidase/glutathione antioxidant system, and oxidatively modified amino acids were measured in subjects with asthma and healthy control subjects.
SOD activity, but not Mn-SOD or Cu,Zn-SOD protein, was lower in asthmatic serum as compared with control, and activity loss was significantly related to airflow limitation. Further, serum SOD activity demonstrated an inverse correlation with circulating levels of 3-bromotyrosine, a posttranslational modification of proteins produced by the eosinophil peroxidase system of eosinophils. Exposure of purified Cu,Zn-SOD to physiologically relevant levels of eosinophil peroxidase-generated reactive brominating species, reactive nitrogen species, or tyrosyl radicals in vitro confirmed that eosinophil-derived oxidative pathways promote enzyme inactivation.
These findings are consistent with greater oxidant stress in asthma leading to greater inactivation of SOD, which likely amplifies inflammation and progressive airflow obstruction.
哮喘气道中氧化应激增加和超氧化物歧化酶(SOD)活性降低与气流受限和高反应性相关。我们假设,氧化应激水平较高的哮喘患者可能有更大程度的SOD活性丧失,这将在全身表现为循环SOD活性丧失,并在临床上表现为严重哮喘的发生和/或气流受限恶化。
为了对此进行研究,我们检测了哮喘患者和健康对照者的血清SOD活性和蛋白质、谷胱甘肽过氧化物酶/谷胱甘肽抗氧化系统以及氧化修饰氨基酸。
与对照组相比,哮喘患者血清中的SOD活性降低,但锰超氧化物歧化酶(Mn-SOD)或铜锌超氧化物歧化酶(Cu,Zn-SOD)蛋白无变化,且活性丧失与气流受限显著相关。此外,血清SOD活性与3-溴酪氨酸的循环水平呈负相关,3-溴酪氨酸是嗜酸性粒细胞嗜酸性粒细胞过氧化物酶系统产生的蛋白质翻译后修饰产物。体外将纯化的Cu,Zn-SOD暴露于生理相关水平的嗜酸性粒细胞过氧化物酶产生的活性溴化物种、活性氮物种或酪氨酰自由基中,证实嗜酸性粒细胞衍生的氧化途径促进酶失活。
这些发现与哮喘中更大的氧化应激导致SOD更大程度失活一致,这可能会放大炎症和进行性气流阻塞。