Limjunyawong Nathachit, Fallica Jonathan, Horton Maureen R, Mitzner Wayne
Environmental Health Sciences, Bloomberg School of Public Health, Johns Hopkins University.
Environmental Health Sciences, Bloomberg School of Public Health, Johns Hopkins University;
J Vis Exp. 2015 Jan 27(95):52376. doi: 10.3791/52376.
In recent decades the mouse has become the primary animal model of a variety of lung diseases. In models of emphysema or fibrosis, the essential phenotypic changes are best assessed by measurement of the changes in lung elasticity. To best understand specific mechanisms underlying such pathologies in mice, it is essential to make functional measurements that can reflect the developing pathology. Although there are many ways to measure elasticity, the classical method is that of the total lung pressure-volume (PV) curve done over the whole range of lung volumes. This measurement has been made on adult lungs from nearly all mammalian species dating back almost 100 years, and such PV curves also played a major role in the discovery and understanding of the function of pulmonary surfactant in fetal lung development. Unfortunately, such total PV curves have not been widely reported in the mouse, despite the fact that they can provide useful information on the macroscopic effects of structural changes in the lung. Although partial PV curves measuring just the changes in lung volume are sometimes reported, without a measure of absolute volume, the nonlinear nature of the total PV curve makes these partial ones very difficult to interpret. In the present study, we describe a standardized way to measure the total PV curve. We have then tested the ability of these curves to detect changes in mouse lung structure in two common lung pathologies, emphysema and fibrosis. Results showed significant changes in several variables consistent with expected structural changes with these pathologies. This measurement of the lung PV curve in mice thus provides a straightforward means to monitor the progression of the pathophysiologic changes over time and the potential effect of therapeutic procedures.
近几十年来,小鼠已成为多种肺部疾病的主要动物模型。在肺气肿或肺纤维化模型中,通过测量肺弹性的变化能最好地评估基本的表型变化。为了深入了解小鼠此类病理状况背后的具体机制,进行能够反映疾病发展过程的功能测量至关重要。尽管测量弹性有多种方法,但经典方法是在整个肺容积范围内绘制全肺压力 - 容积(PV)曲线。近100年来,几乎对所有哺乳动物物种的成年肺都进行过这种测量,而且此类PV曲线在胎儿肺发育过程中肺表面活性物质功能的发现和理解方面也发挥了重要作用。遗憾的是,尽管全肺PV曲线能够提供有关肺结构变化宏观效应的有用信息,但在小鼠中尚未得到广泛报道。虽然有时会报道仅测量肺容积变化的部分PV曲线,但由于缺乏绝对容积的测量,全肺PV曲线的非线性性质使得这些部分曲线很难解释。在本研究中,我们描述了一种测量全肺PV曲线的标准化方法。然后,我们在两种常见的肺部疾病——肺气肿和肺纤维化中,测试了这些曲线检测小鼠肺结构变化的能力。结果显示,与这些疾病预期的结构变化一致,几个变量有显著变化。因此,对小鼠肺PV曲线的这种测量提供了一种直接的方法,来监测病理生理变化随时间的进展以及治疗程序的潜在效果。