Kim Hojoong, Park Hyun A, Suh Gee Young, Chung Man Pyo, Kwon O Jung
Division of Pulmonary and Critical Care Medicine, Department of Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.
Exp Lung Res. 2002 Jul-Aug;28(5):351-9. doi: 10.1080/01902140290091985.
There is increasing evidence that endothelin (ET) and endothelial nitric oxide synthase (eNOS) may contribute various kinds of pulmonary vascular remodeling, including postobstructive pulmonary vasculopathy (POPV), which resulted from chronic ligation of unilateral pulmonary artery. The aim of this study was to investigate the expression of ET-1, ET-A receptor, ET-B receptor, and eNOS quantitatively in POPV rats. One month after a left thoracotomy with either left main pulmonary artery ligation (ligated group) or no ligation (control group), rat pulmonary arteries and lungs were used for Western blot analysis using specific antibodies against ET-1, ET-A receptor, ET-B receptor, and eNOS. ET-A receptor was more highly expressed in the pulmonary arteries of ligated rats compared to the control. The expression of ET-1, ET-B receptor,and eNOS was not different between ligated and control rats. These findings suggest that ET-A receptor overexpression would play a main role for pulmonary arterial remodeling in POPV rats, whereas eNOS may serve as a compensatory mediator.
越来越多的证据表明,内皮素(ET)和内皮型一氧化氮合酶(eNOS)可能参与各种肺血管重塑,包括由单侧肺动脉慢性结扎引起的阻塞后肺血管病(POPV)。本研究的目的是定量研究ET-1、ET-A受体、ET-B受体和eNOS在POPV大鼠中的表达。在进行左主肺动脉结扎的左胸切开术1个月后(结扎组)或未结扎(对照组),使用针对ET-1、ET-A受体、ET-B受体和eNOS的特异性抗体,对大鼠肺动脉和肺进行蛋白质印迹分析。与对照组相比,结扎大鼠肺动脉中ET-A受体的表达更高。结扎大鼠和对照大鼠之间ET-1、ET-B受体和eNOS的表达没有差异。这些发现表明,ET-A受体的过表达在POPV大鼠的肺动脉重塑中起主要作用,而eNOS可能作为一种代偿介质。