Respiratory Medicine Research Programme, Centre for Infection and Immunity, Queen’s University, Belfast, Northern Ireland.
Am J Physiol Lung Cell Mol Physiol. 2011 Mar;300(3):L305-18. doi: 10.1152/ajplung.00223.2010. Epub 2010 Nov 26.
Pulmonary fluid clearance is regulated by the active transport of Na(+) and Cl(-) through respiratory epithelial ion channels. Ion channel dysfunction contributes to the pathogenesis of various pulmonary fluid disorders including high-altitude pulmonary edema (HAPE) and neonatal respiratory distress syndrome (RDS). Nasal potential difference (NPD) measurement allows an in vivo investigation of the functionality of these channels. This technique has been used for the diagnosis of cystic fibrosis, the archetypal respiratory ion channel disorder, for over a quarter of a century. NPD measurements in HAPE and RDS suggest constitutive and acquired dysfunction of respiratory epithelial Na(+) channels. Acute lung injury (ALI) is characterized by pulmonary edema due to alveolar epithelial-interstitial-endothelial injury. NPD measurement may enable identification of critically ill ALI patients with a susceptible phenotype of dysfunctional respiratory Na(+) channels and allow targeted therapy toward Na(+) channel function.
肺液清除受呼吸上皮离子通道主动转运 Na(+) 和 Cl(-) 的调节。离子通道功能障碍导致各种肺液紊乱的发病机制,包括高原肺水肿 (HAPE) 和新生儿呼吸窘迫综合征 (RDS)。鼻电位差 (NPD) 测量允许对这些通道的功能进行体内研究。这项技术已经用于诊断囊性纤维化,这是一种典型的呼吸离子通道疾病,已经使用了超过四分之一个世纪。HAPE 和 RDS 的 NPD 测量表明呼吸上皮 Na(+) 通道的组成型和获得性功能障碍。急性肺损伤 (ALI) 的特征是由于肺泡上皮-间质-内皮损伤导致的肺水肿。NPD 测量可能能够识别具有功能障碍呼吸 Na(+) 通道易感性表型的危重症 ALI 患者,并允许针对 Na(+) 通道功能进行靶向治疗。