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Published ahead of print on January 7, 2004, doi:10.1164/rccm.200310-1417OC
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American Journal of Respiratory and Critical Care Medicine Vol 169. pp. 739-748, (2004)
© 2004 American Thoracic Society


Original Article

High Tidal Volume Ventilation Causes Different Inflammatory Responses in Newborn versus Adult Lung

Ian B. Copland, Francisco Martinez, Brian P. Kavanagh, Doreen Engelberts, Colin McKerlie, Jaques Belik and Martin Post

Program in Lung Biology and Department of Critical Care Medicine, The Hospital for Sick Children; Departments of Laboratory Medicine and Pathobiology and Pediatrics, University of Toronto, Toronto, Ontario, Canada; and Department of Pediatrics, University of Sao Paulo, Ribeirao Preto, Sao Paulo, Brazil

Correspondence and requests for reprints should be addressed to Martin Post, Ph.D., Lung Biology Program, The Hospital for Sick Children, 555 University Avenue, Toronto, ON, M5G 1X8 Canada. E-mail: martin.post{at}sickkids.ca

We investigated the effect of high VT ventilation on adult and newborn rats by examining pulmonary injury and cytokine messenger RNA (mRNA). On the basis of compliance, edema formation, and histology, ventilation with 25 ml·kg-1 was more injurious to adult rats than newborns. Ventilation with 40 ml kg-1 minimally affected compliance in newborns but caused death in adults. Ventilation of adults for 30 minutes at 25 ml kg-1 upregulated the mRNA expression of interleukin (IL)-1ß, IL-6, tumor necrosis factor-{alpha} (TNF-{alpha}), macrophage inflammatory protein-2 (MIP-2), and IL-10, whereas in newborns such ventilation only increased mRNA expression of MIP-2 and IL-10. When VT was raised to 40 ml kg-1 in newborns, IL-1ß mRNA levels were additionally increased at 30 minutes, whereas ventilation for 3 hours additionally increased IL-6 and TNF-{alpha} mRNA. In newborns, the addition of 100% oxygen (O2) to 30 minutes of ventilation blunted the high VT induction of IL-1ß, IL-10, and MIP-2 mRNA expressions, whereas at 3 hours, 100% O2 concentration synergistically increased the mRNAs for TNF-{alpha} and IL-6. Overall, adult rats are more susceptible to high VT–induced lung injury compared with newborns. In newborns, the inflammatory response is dependent on VT, duration, and supplemental O2. Thus, recommendations for VT limitation based on adult data may be inappropriate for newborns.

Key Words: VT • oxygen • cytokines • lung maturity




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