Elliott Jonathan E, Mantilla Carlos B, Pabelick Christina M, Roden Anja C, Sieck Gary C
Mayo Clinic, Department of Physiology and Biomedical Engineering, Rochester, Minnesota;
Mayo Clinic, Department of Physiology and Biomedical Engineering, Rochester, Minnesota; Mayo Clinic, Department of Anesthesiology, Rochester, Minnesota; and.
Am J Physiol Lung Cell Mol Physiol. 2016 Jul 1;311(1):L167-76. doi: 10.1152/ajplung.00232.2016. Epub 2016 Jun 10.
Previous work investigating respiratory system mechanics in mice has reported an aging-related increase in compliance and mean linear intercept (Lm). However, these changes were assessed using only a young (2-mo-old) and old (20- and 26-mo-old) group yet were interpreted to reflect a linear evolution across the life span. Therefore, to investigate respiratory system mechanics and lung morphometry across a more complete spectrum of ages, we utilized 2 (100% survival, n = 6)-, 6 (100% survival, n = 12)-, 18 (90% survival, n = 12)-, 24 (75% survival, n = 12)-, and 30 (25% survival, n = 12)-mo-old C57BL/6 mice. We found a nonlinear aging-related decrease in respiratory system resistance and increase in dynamic compliance and hysteresis between 2- and 24-mo-old mice. However, in 30-mo-old mice, respiratory system resistance increased, and dynamic compliance and hysteresis decreased relative to 24-mo-old mice. Respiratory system impedance spectra were measured between 1-20.5 Hz at positive end-expiratory pressures (PEEP) of 1, 3, 5, and 7 cmH2O. Respiratory system resistance and reactance at each level of PEEP were increased and decreased, respectively, only in 2-mo-old animals. No differences in the respiratory system impedance spectra were observed in 6-, 18-, 24-, and 30-mo-old mice. Additionally, lungs were fixed following tracheal instillation of 4% paraformaldehyde at 25 cmH2O and processed for Lm and airway collagen deposition. There was an aging-related increase in Lm consistent with emphysematous-like changes and no evidence of increased airway collagen deposition. Accordingly, we demonstrate nonlinear aging-related changes in lung mechanics and morphometry in C57BL/6 mice.
以往对小鼠呼吸系统力学的研究报告称,顺应性和平均线性截距(Lm)会随着年龄增长而增加。然而,这些变化仅在年轻(2月龄)和年老(20月龄及26月龄)组中进行了评估,却被解释为反映了整个生命周期中的线性演变。因此,为了在更完整的年龄范围内研究呼吸系统力学和肺形态测量,我们使用了2月龄(存活率100%,n = 6)、6月龄(存活率100%,n = 12)、18月龄(存活率90%,n = 12)、24月龄(存活率75%,n = 12)和30月龄(存活率25%,n = 12)的C57BL/6小鼠。我们发现,在2至24月龄的小鼠中,呼吸系统阻力呈现与年龄相关的非线性下降,动态顺应性和滞后现象增加。然而,与24月龄小鼠相比,30月龄小鼠的呼吸系统阻力增加,动态顺应性和滞后现象减少。在呼气末正压(PEEP)为1、3、5和7 cmH₂O时,于1至20.5 Hz测量呼吸系统阻抗谱。仅在2月龄动物中,每个PEEP水平下的呼吸系统阻力和电抗分别增加和降低。在6、18、24和30月龄小鼠中未观察到呼吸系统阻抗谱的差异。此外,在气管内注入25 cmH₂O的4%多聚甲醛后固定肺部,并对Lm和气道胶原沉积进行处理。Lm呈现与年龄相关的增加,与肺气肿样变化一致,且没有气道胶原沉积增加的证据。因此,我们证明C57BL/6小鼠的肺力学和形态测量存在与年龄相关的非线性变化。