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Protective effects of elevated endogenous surfactant pools to injurious mechanical ventilation.

Authors :
Yamashita, Cory
Forbes, Amy
Tessolini, Jenna M.
Li-juan Yao
Lewis, James F.
Veldhuizen, Ruud A. W.
Source :
American Journal of Physiology: Lung Cellular & Molecular Physiology. Apr2008, Vol. 294, pL724-L732. 9p. 2 Charts, 7 Graphs.
Publication Year :
2008

Abstract

Yamashita C, Forbes A, Tessolini JM, Yao L-J, Lewis JF, Veidhuizen RA. Protective effects of elevated endogenous surfactant pools to injurious mechanical ventilation. Am J Physiol Lung Cell Mo! Physiol 294: L724-L732, 2008. First published January 25, 2008; doi: 10.11 52/ajplung.00389.2007.-Depletion of alveolar macrophages (AM) leads to an increase in endogenous surfactant that lasts several days beyond the repletion of AM. Furthermore, impairment to the endogenous pulmonary surfactant system contributes to ventilation- induced lung injury. The objective of the current study was to determine whether increased endogenous surfactant pools induced via AM depletion was protective against ventilation-induced lung injury. Adult rats were intratracheally instilled with either control or dichlo- romethylene diphosphonic acid (DMDP) containing liposomes to deplete AMs and thereby increase endogenous surfactant pools. Either 3 or 7 days following instillation, rats were exposed to 2 h of injurious ventilation using either an ex vivo or in vivo ventilation protocol and were compared with nonventilated controls. The measured outcomes were oxygenation, lung compliance, lavage protein, and inflammatory cytokine concentrations. Compared with controls, the DMDP-treated animals had significantly reduced AM numbers and increased surfac- tant pools 3 days after instillation. Seven days after instillation, AM numbers had returned to normal, but surfactant pools were still elevated. DMDP-treated animals at both time points exhibited pro- tection against ventilation-induced lung injury, which included supe- rior physiological parameters, lower protein leakage, and lower in- flammatory mediator release into the air space, compared with ani- mals not receiving DMDP. It is concluded that DMDP-liposome administration protects against ventilation-induced lung injury. This effect appears to be due to the presence of elevated endogenous surfactant pools. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
10400605
Volume :
294
Database :
Academic Search Index
Journal :
American Journal of Physiology: Lung Cellular & Molecular Physiology
Publication Type :
Academic Journal
Accession number :
31887274
Full Text :
https://doi.org/10.1152/ajplung.00389.2007