Sly Peter D, Collins Rachel A, Thamrin Cindy, Turner Debra J, Hantos Zoltan
Division of Clinical Sciences, Telethon Institute for Child Health Research, School of Child Health, University of Western Australia, West Perth, Western Australia 6875, Australia.
J Appl Physiol (1985). 2003 Apr;94(4):1460-6. doi: 10.1152/japplphysiol.00596.2002. Epub 2002 Aug 30.
We measured respiratory input impedance (1-25 Hz) in mice and obtained parameters for airway and tissue mechanics by model fitting. Lung volume was varied by inflating to airway opening pressure (Pao) between 0 and 20 cm H2O. The expected pattern of changes in respiratory mechanics with increasing lung volume was seen: a progressive fall in airway resistance and increases in the coefficients of tissue damping and elastance. A surprising pattern was seen in hysteresivity (eta), with a plateau at low lung volumes (Pao < 10 cm H2O), a sharp fall occurring between 10 and 15 cm H2O, and eta approaching a second (lower) plateau at higher lung volumes. Studies designed to elucidate the mechanism(s) behind this behavior revealed that this was not due to chest wall properties, differences in volume history at low lung volume, time dependence of volume recruitment, or surface-acting forces. Our data are consistent with the notion that at low lung volumes the mechanics of the tissue matrix determine eta, whereas at high lung volumes the properties of individual fibers (collagen) become more important.
我们测量了小鼠的呼吸输入阻抗(1 - 25赫兹),并通过模型拟合获得了气道和组织力学的参数。通过将肺充气至气道开口压力(Pao)在0至20厘米水柱之间来改变肺容积。观察到随着肺容积增加呼吸力学变化的预期模式:气道阻力逐渐下降,组织阻尼系数和弹性增加。在滞后率(eta)方面观察到一种令人惊讶的模式,在低肺容积(Pao < 10厘米水柱)时出现平台期,在10至15厘米水柱之间急剧下降,并且在较高肺容积时eta接近第二个(较低的)平台期。旨在阐明这种行为背后机制的研究表明,这不是由于胸壁特性、低肺容积时容积历史的差异、容积募集的时间依赖性或表面作用力。我们的数据与以下观点一致,即在低肺容积时组织基质的力学决定eta,而在高肺容积时单个纤维(胶原蛋白)的特性变得更为重要。