Kornecki Alik, Tsuchida Shinya, Ondiveeran Hari Kumar, Engelberts Doreen, Frndova Helena, Tanswell A Keith, Post Martin, McKerlie Colin, Belik Jaques, Fox-Robichaud Alison, Kavanagh Brian P
Lung Biology Program, Department of Critical Care Medicine, Hospital for Sick Children, 555 University Avenue, Toronto, ON, Canada M5G 1X8.
Am J Respir Crit Care Med. 2005 Apr 1;171(7):743-52. doi: 10.1164/rccm.200408-1053OC. Epub 2005 Jan 7.
Ventilator-induced lung injury has been predominantly studied in adults.
To explore the effects of age and lung development on susceptibility to such injury.
Ex vivo isolated nonperfused rat lungs (infant, juvenile, and adult) were mechanically ventilated where VT was based on milliliters per kilogram of body weight or as a percentage of the measured total lung capacity (TLC). In vivo anesthetized rats (infant, adult) were mechanically ventilated with pressure-limited VTs. Allocation to ventilation strategy was randomized.
Ex vivo injury was assessed by pressure-volume analysis, reduction in TLC, and histology, and in vivo injury by lung compliance, cytokine production, and wet- to dry-weight ratio.
Ex vivo ventilation (VT 30 ml.kg(-1)) resulted in a significant reduction (36.0 +/- 10.1%, p < 0.05) in TLC in adult but not in infant lungs. Ex vivo ventilation (VT 50% TLC) resulted in a significant reduction in TLC in both adult (27.8 +/- 2.8%) and infant (10.6 +/- 7.0%) lungs, but more so in the adult lungs (p < 0.05); these changes were paralleled by histology and pressure-volume characteristics. After high stretch in vivo ventilation, adult but not infant rats developed lung injury (total lung compliance, wet/dry ratio, tumor necrosis factor alpha). Surface video microscopy demonstrated greater heterogeneity of alveolar distension in ex vivo adult versus infant lungs.
These data provide ex vivo and in vivo evidence that comparable ventilator settings are significantly more injurious in the adult than infant rat lung, probably reflecting differences in intrinsic susceptibility or inflation pattern.
呼吸机诱导的肺损伤主要在成人中进行研究。
探讨年龄和肺发育对这种损伤易感性的影响。
对离体未灌注的大鼠肺(婴儿、幼年和成年)进行机械通气,潮气量基于每千克体重的毫升数或作为测量的总肺容量(TLC)的百分比。在体内,对麻醉的大鼠(婴儿、成年)进行压力限制潮气量的机械通气。通气策略的分配是随机的。
通过压力-容积分析、TLC降低和组织学评估离体损伤,通过肺顺应性、细胞因子产生和湿重与干重比评估体内损伤。
离体通气(潮气量30 ml·kg⁻¹)导致成年大鼠肺的TLC显著降低(36.0±10.1%,p<0.05),但婴儿大鼠肺未出现此情况。离体通气(潮气量50% TLC)导致成年(27.8±2.8%)和婴儿(10.6±7.0%)大鼠肺的TLC均显著降低,但成年大鼠肺降低更明显(p<0.05);这些变化与组织学和压力-容积特征一致。在体内进行高张力通气后,成年大鼠而非婴儿大鼠出现肺损伤(总肺顺应性、湿/干比、肿瘤坏死因子α)。表面视频显微镜显示,离体成年大鼠肺与婴儿大鼠肺相比,肺泡扩张的异质性更大。
这些数据提供了离体和体内证据,表明相同的呼吸机设置对成年大鼠肺的损伤明显大于婴儿大鼠肺,这可能反映了内在易感性或充气模式的差异。