Molecular Physiology and Rehabilitation Research Laboratory, Radiologic Sciences and Respiratory Therapy Division, School of Health and Rehabilitation Sciences, The Ohio State University College of Medicine, The Ohio State University Wexner Medical Center, Columbus, Ohio.
Exercise and Sport Nutrition Laboratory, Department of Health and Kinesiology, Texas A&M University, College Station, Texas.
Ann Allergy Asthma Immunol. 2014 Jan;112(1):18-22. doi: 10.1016/j.anai.2013.10.007. Epub 2013 Nov 6.
To investigate the molecular mechanism of reactive nitrogen species (RNS) in the pathogenesis of asthma and examine the use of fractional exhaled nitric oxide (FENO) measurements in close conjunction with standard clinical assessments of asthma.
Through PubMed, Google Scholar, and Medline databases, a broad medical literature review was performed in the following areas of asthma pathobiology and management: allergic asthma, RNS, nitric oxide (NO), airway inflammation, and FENO.
Studies were selected based on the physiologic and pathophysiologic roles of RNS in relation to allergic asthma. Current evaluations on clinical applications of FENO in asthma treatment also were selected.
At the onset of an asthma attack, an enhanced production of NO strongly correlates with increase inducible NO synthase (NOS) activity, whereas endothelial NOS and neuronal NOS regulate primarily normal metabolic functions in the central and peripheral airways. During allergic inflammatory responses, NO and superoxide form peroxynitrite, which has deleterious effects in the respiratory tract. RNS directly accentuates airway inflammation and cytotoxicity through nitrosative stress. Moreover, the use of FENO to monitor eosinophilic-mediated airway inflammation is a potentially valuable assessment that supplements standard procedures to monitor the progression of asthma.
This review examines recent evidence implicating the molecular mechanisms of NO and NO-derived RNS in the pathobiology of asthma and suggests that monitoring FENO may markedly contribute to asthma diagnosis.
探讨活性氮物种(RNS)在哮喘发病机制中的分子机制,并研究在密切结合哮喘标准临床评估的情况下,利用呼出气一氧化氮(FENO)测量的效果。
通过 PubMed、Google Scholar 和 Medline 数据库,对哮喘病理生物学和管理的以下领域进行了广泛的医学文献综述:过敏性哮喘、RNS、一氧化氮(NO)、气道炎症和 FENO。
根据 RNS 与过敏性哮喘的关系,选择了与 RNS 的生理和病理生理作用有关的研究。还选择了当前关于 FENO 在哮喘治疗中的临床应用的评估。
在哮喘发作开始时,NO 的产生增加与诱导型一氧化氮合酶(NOS)活性的增加强烈相关,而内皮型 NOS 和神经元型 NOS 主要调节中枢和外周气道的正常代谢功能。在过敏性炎症反应中,NO 和超氧化物形成过氧亚硝酸盐,对呼吸道有有害影响。RNS 通过硝化应激直接加重气道炎症和细胞毒性。此外,利用 FENO 监测嗜酸性粒细胞介导的气道炎症是一种潜在有价值的评估方法,可补充监测哮喘进展的标准程序。
这篇综述检查了最近的证据,这些证据表明 NO 和由 NO 衍生的 RNS 的分子机制在哮喘的病理生物学中起作用,并表明监测 FENO 可能对哮喘诊断有显著贡献。