Department of Physiology and Cell Biology, University of South Alabama , Mobile, Alabama.
Center for Lung Biology, University of South Alabama , Mobile, Alabama.
Am J Physiol Lung Cell Mol Physiol. 2018 May 1;314(5):L835-L845. doi: 10.1152/ajplung.00201.2017. Epub 2018 Jan 18.
Here, we tested the hypothesis that severe pulmonary arterial hypertension impairs retrograde perfusion. To test this hypothesis, pulmonary arterial hypertension was induced in Fischer rats using a single injection of Sugen 5416 followed by 3 wk of exposure to 10% hypoxia and then 2 wk of normoxia. This Sugen 5416 and hypoxia regimen caused severe pulmonary arterial hypertension, with a Fulton index of 0.73 ± 0.07, reductions in both the pulmonary arterial acceleration time and pulmonary arterial acceleration to pulmonary arterial ejection times ratio, and extensive medial hypertrophy and occlusive neointimal lesions. Whereas the normotensive circulation accommodated large increases in forward and retrograde flow, the hypertensive circulation did not. During forward flow, pulmonary artery and double occlusion pressures rose sharply at low perfusion rates, resulting in hydrostatic edema. Pulmonary arterial hypertensive lungs possessed an absolute intolerance to retrograde perfusion, and they rapidly developed edema. Retrograde perfusion was not rescued by maximal vasodilation. Retrograde perfusion was preserved in lungs from animals treated with Sugen 5416 and hypoxia for 1 and 3 wk, in lungs from animals with a milder form of hypoxic hypertension, and in normotensive lungs subjected to high outflow pressures. Thus impaired retrograde perfusion coincides with development of severe pulmonary arterial hypertension, with advanced structural defects in the microcirculation.
在这里,我们检验了这样一个假设,即严重的肺动脉高压会损害逆行灌注。为了验证这一假设,我们使用苏根 5416 单次注射,然后暴露于 10%低氧 3 周,再暴露于常氧 2 周,在费歇尔大鼠中诱导肺动脉高压。这种苏根 5416 和低氧方案导致严重的肺动脉高压,富尔顿指数为 0.73±0.07,肺动脉加速度时间和肺动脉加速度至肺动脉射血时间比均降低,以及广泛的中膜肥厚和闭塞性新生内膜病变。虽然正常血压循环能够适应前向和逆行血流的大量增加,但高血压循环不能。在前向血流中,肺动脉和双重闭塞压在低灌注率下急剧升高,导致静水水肿。肺动脉高压肺对逆行灌注绝对不耐受,它们迅速发生水肿。最大血管扩张不能挽救逆行灌注。在苏根 5416 和低氧处理 1 周和 3 周的动物的肺、低氧高血压动物中较轻形式的肺和处于高流出压力的正常血压肺中,逆行灌注得以保留。因此,逆行灌注受损与严重肺动脉高压的发展相一致,伴有微循环的严重结构缺陷。