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J Appl Physiol 103: 1551-1559, 2007. First published August 9, 2007; doi:10.1152/japplphysiol.00006.2007
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Effects of reduced tidal volume ventilation on pulmonary function in mice before and after acute lung injury

Apiradee Thammanomai,1 Arnab Majumdar,1 Erzsébet Bartolák-Suki,1,2 and Béla Suki1

1Department of Biomedical Engineering, Boston University, Boston; and 2CelluTraf Sci., Boston, Massachusetts

Submitted 2 January 2007 ; accepted in final form 2 August 2007

We investigated the influence of load impedance on ventilator performance and the resulting effects of reduced tidal volume (VT) on lung physiology during a 30-min ventilation of normal mice and 10 min of additional ventilation following lavage-induced injury at two positive end-expiratory pressure (PEEP) levels. Respiratory mechanics were regularly monitored, and the lavage fluid was tested for the soluble E-cadherin, an epithelial cell adhesion molecule, and surfactant protein (SP) B. The results showed that, due to the load dependence of the delivered VT from the small-animal ventilator: 1) uncontrolled ventilation in normal mice resulted in a lower delivered VT (6 ml/kg at 3-cmH2O PEEP and 7 ml/kg at 6-cmH2O PEEP) than the prescribed VT (8 ml/kg); 2) at 3-cmH2O PEEP, uncontrolled ventilation in normal mice led to an increase in lung parenchymal functional heterogeneity, a reduction of SP-B, and an increase in E-cadherin; 3) at 6-cmH2O PEEP, ventilation mode had less influence on these parameters; and 4) in a lavage model of acute respiratory distress syndrome, delivered VT decreased to 4 ml/kg from the prescribed 8 ml/kg, which resulted in severely compromised lung function characterized by increases in lung elastance, airway resistance, and alveolar tissue heterogeneity. Furthermore, the low VT ventilation also resulted in poor survival rate independent of PEEP. These results highlight the importance of delivering appropriate VT to both the normal and injured lungs. By leaving the VT uncompensated, it can significantly alter physiological and biological responses in mice.

mechanics; load dependence; surfactant protein; E-cadherin; heterogeneity



Address for reprint requests and other correspondence: B. Suki, Dept. of Biomedical Engineering, Boston Univ., Boston, MA 02215 (e-mail: bsuki{at}bu.edu)




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A. Thammanomai, L. E. Hueser, A. Majumdar, E. Bartolak-Suki, and B. Suki
Design of a new variable-ventilation method optimized for lung recruitment in mice
J Appl Physiol, May 1, 2008; 104(5): 1329 - 1340.
[Abstract] [Full Text] [PDF]




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