Emami Kiarash, Cadman Robert V, Woodburn John M, Fischer Martin C, Kadlecek Stephen J, Zhu Jianliang, Pickup Stephen, Guyer Richard A, Law Michelle, Vahdat Vahid, Friscia Michael E, Ishii Masaru, Yu Jiangsheng, Gefter Warren B, Shrager Joseph B, Rizi Rahim R
Dept. of Radiology, University of Pennsylvania, B1 Stellar-Chance Laboratories, 422 Curie Blvd., Philadelphia, PA 19104-6100, USA.
J Appl Physiol (1985). 2008 Mar;104(3):773-86. doi: 10.1152/japplphysiol.00482.2007. Epub 2007 Dec 6.
Early changes of lung function and structure were studied in the presence of an elastase-induced model of emphysema in 35 Sprague-Dawley rats at mild (5 U/100 g) and moderate (10 U/100 g) severities. Lung ventilation was measured on a regional basis (at a planar resolution of 3.2 mm) by hyperpolarized 3He MRI at 5 and 10 wk after model induction. Subsequent to imaging, average alveolar diameter was measured from histological slices taken from the centers of each lobe. Changes of mean fractional ventilation, mean linear intercept, and intrasubject heterogeneity of ventilation were studied during disease progression. Mean fractional ventilation was significantly different between healthy controls (0.23 +/- 0.04) and emphysematous animals at both time points in the 10-unit group (0.06 +/- 0.02 and 0.12 +/- 0.05, respectively). Changes in average alveolar diameter were not statistically observable until the 10th wk between healthy (37 +/- 10 microm) and emphysematous rats (73 +/- 25 and 95 +/- 31 microm, for 5 and 10 units, respectively). Assessment of function-structure correlation suggested that the majority of the decline in fractional ventilation occurred in the first 5 wk, while enlargement of alveolar diameters appeared primarily between the 5th and 10th wk. A thresholding metric, based on the 20th percentile of fractional ventilation over the entire lung, was utilized to detect the onset of the disease with confidence, independent of whether the regional ventilation measurements were normalized with respect to the delivered tidal volume and estimated functional residual capacity of each individual rat.
在35只斯普拉格-道利大鼠中,利用弹性蛋白酶诱导的肺气肿模型,研究了轻度(5 U/100 g)和中度(10 U/100 g)严重程度下肺功能和结构的早期变化。在模型诱导后5周和10周,通过超极化3He MRI在区域基础上(平面分辨率为3.2 mm)测量肺通气。成像后,从每个肺叶中心获取的组织学切片测量平均肺泡直径。研究了疾病进展过程中平均通气分数、平均线性截距和通气的个体内异质性的变化。在10单位组的两个时间点,健康对照组(0.23±0.04)和肺气肿动物的平均通气分数均有显著差异(分别为0.06±0.02和0.12±0.05)。直到第10周,健康大鼠(37±10微米)和肺气肿大鼠(5单位组为73±25微米,10单位组为95±31微米)之间的平均肺泡直径变化才具有统计学意义。功能-结构相关性评估表明,通气分数的下降主要发生在最初的5周,而肺泡直径的增大主要出现在第5周和第10周之间。基于整个肺通气分数第20百分位数的阈值度量被用于可靠地检测疾病的发作,而不管区域通气测量是否相对于每只大鼠的潮气量和估计的功能残气量进行了归一化。