Fields Michael J, Bishai John M, Mitzner Wayne, Wagner Elizabeth M
Department of Pediatrics, Johns Hopkins University, Baltimore, Maryland, USA.
Am J Physiol Lung Cell Mol Physiol. 2007 Jul;293(1):L254-8. doi: 10.1152/ajplung.00398.2006. Epub 2007 Apr 20.
Pulmonary ischemia resulting from chronic pulmonary embolism leads to proliferation of the systemic circulation within and surrounding the lung. However, it is not clear how well alveolar tissue is sustained during the time of complete pulmonary ischemia. In the present study, we investigated how pulmonary ischemia after left pulmonary artery ligation (LPAL) would alter lung mechanical properties and morphology. In this established mouse model of lung angiogenesis after chronic LPAL (10), we evaluated lung function and structure before (3 days) and after (14 days) a functional systemic circulation to the left lung is established. Age-matched naïve and sham-operated C57Bl/6 mice and mice undergoing chronic LPAL were studied. Left and right lung pressure-volume relationships were determined. Next, lungs were inflated in situ with warmed agarose (25-30 cmH(2)O) and fixed, and mean chord lengths (MCL) of histological sections were quantified. MCL of naïve mice averaged 43.9 +/- 1.8 mum. No significant changes in MCL were observed at either time point after LPAL. Left lung volumes and specific compliances were significantly reduced 3 days after LPAL. However, by 14 days after LPAL, lung pressure-volume relationships were not different from controls. These results suggest that severe pulmonary ischemia causes changes in lung mechanics early after LPAL that are reversed by the time a new systemic vasculature is known to perfuse pulmonary capillaries. The LPAL model thus affords a unique opportunity to study lung functional responses to tissue ischemia and subsequent recovery.
慢性肺栓塞导致的肺缺血会引起肺内及肺周围体循环的增生。然而,在完全性肺缺血期间肺泡组织的维持情况尚不清楚。在本研究中,我们调查了左肺动脉结扎(LPAL)后的肺缺血如何改变肺的力学特性和形态。在这个已建立的慢性LPAL后肺血管生成的小鼠模型中(10),我们评估了在左肺建立功能性体循环之前(3天)和之后(14天)的肺功能和结构。研究了年龄匹配的未经处理的、假手术的C57Bl/6小鼠以及接受慢性LPAL的小鼠。测定了左肺和右肺的压力-容积关系。接下来,用温热的琼脂糖(25 - 30 cmH₂O)对肺进行原位充气并固定,对组织学切片的平均弦长(MCL)进行量化。未经处理的小鼠的MCL平均为43.9±1.8μm。LPAL后两个时间点的MCL均未观察到显著变化。LPAL后3天,左肺容积和比顺应性显著降低。然而,到LPAL后14天,肺压力-容积关系与对照组无差异。这些结果表明,严重的肺缺血在LPAL后早期会引起肺力学的改变,而当已知新的体循环血管灌注肺毛细血管时,这些改变会被逆转。因此,LPAL模型为研究肺对组织缺血及随后恢复的功能反应提供了一个独特的机会。