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小鼠肺组织的异质性:弹性蛋白酶处理的影响。

Tissue heterogeneity in the mouse lung: effects of elastase treatment.

作者信息

Ito Satoru, Ingenito Edward P, Arold Stephen P, Parameswaran Harikrishnan, Tgavalekos Nora T, Lutchen Kenneth R, Suki Béla

机构信息

Department of Biomedical Engineering, Boston University, Boston, MA 02215, USA.

出版信息

J Appl Physiol (1985). 2004 Jul;97(1):204-12. doi: 10.1152/japplphysiol.01246.2003. Epub 2004 Mar 12.

DOI:10.1152/japplphysiol.01246.2003
PMID:15020580
Abstract

We developed a network model in an attempt to characterize heterogeneity of tissue elasticity of the lung. The model includes a parallel set of pathways, each consisting of an airway resistance, an airway inertance, and a tissue element connected in series. The airway resistance, airway inertance, and the hysteresivity of the tissue elements were the same in each pathway, whereas the tissue elastance (H) followed a hyperbolic distribution between a minimum and maximum. To test the model, we measured the input impedance of the respiratory system of ventilated normal and emphysematous C57BL/6 mice in closed chest condition at four levels of positive end-expiratory pressures. Mild emphysema was developed by nebulized porcine pancreatic elastase (PPE) (30 IU/day x 6 days). Respiratory mechanics were studied 3 wk following the initial treatment. The model significantly improved the fitting error compared with a single-compartment model. The PPE treatment was associated with an increase in mean alveolar diameter and a decrease in minimum, maximum, and mean H. The coefficient of variation of H was significantly larger in emphysema (40%) than that in control (32%). These results indicate that PPE treatment resulted in increased time-constant inequalities associated with a wider distribution of H. The heterogeneity of alveolar size (diameters and area) was also larger in emphysema, suggesting that the model-based tissue elastance heterogeneity may reflect the underlying heterogeneity of the alveolar structure.

摘要

我们开发了一种网络模型,试图描述肺组织弹性的异质性。该模型包括一组并行的通路,每条通路由气道阻力、气道惯性和串联连接的组织元件组成。每条通路中的气道阻力、气道惯性和组织元件的滞后性相同,而组织弹性(H)在最小值和最大值之间呈双曲线分布。为了测试该模型,我们在四个呼气末正压水平下,测量了通气的正常和肺气肿C57BL/6小鼠在闭胸状态下呼吸系统的输入阻抗。通过雾化猪胰弹性蛋白酶(PPE)(30 IU/天×6天)诱导轻度肺气肿。在初始治疗后3周研究呼吸力学。与单室模型相比,该模型显著改善了拟合误差。PPE治疗与平均肺泡直径增加以及最小、最大和平均H降低有关。肺气肿中H的变异系数(40%)显著大于对照组(32%)。这些结果表明,PPE治疗导致与更广泛的H分布相关的时间常数不平等增加。肺气肿中肺泡大小(直径和面积)的异质性也更大,这表明基于模型的组织弹性异质性可能反映了肺泡结构的潜在异质性。

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