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Published ahead of print on June 7, 2007, doi:10.1165/rcmb.2006-0434OC

Am. J. Respir. Cell Mol. Biol., Volume 37, Number 4, October 2007, 387-394

A more recent version of this article appeared on October 1, 2007
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Submitted on November 21, 2006
Revised on June 7, 2007

Activity and Inhibition Resistance of a Phospholipase-Resistant Synthetic Surfactant in Rat Lungs

Zhengdong Wang1, Yusuo Chang1, Adrian L Schwan2, and Robert H Notter3*

1 Department of Pediatrics, University of Rochester School of Medicine, Rochester, NY, United States, 2 Department of Chemistry, University of Guelph, Guelph, Ontario, Canada, 3 Department of Pediatrics, University of Rochester School of Medicine, Rochester, NY, United States; Department of Environmental Medicine, University of Rochester School of Medicine, Rochester, NY, USA

* To whom correspondence should be addressed. E-mail: robert_notter{at}urmc.rochester.edu.

This study investigates the activity and inhibition resistance in excised rat lungs of a novel synthetic surfactant containing the phospholipase-resistant diether phosphonolipid DEPN-8 plus 1.5% bovine surfactant protein (SP)-B/C compared to calf lung surfactant extract (CLSE). DEPN-8 + 1.5% SP-B/C surpassed CLSE in normalizing surfactant-deficient pressure-volume (P-V) deflation mechanics in lavaged excised lungs in the presence of phospholipase A2 (PLA2) or C18:1 lyso-phosphatidylcholine (LPC). DEPN-8 + 1.5% SP-B/C had ctivity equal to CLSE in normalizing P-V mechanics in the absence of inhibitors or in the presence of serum albumin. These physiological activity findings were directly consistent with surface activity measurements on the pulsating bubble surfactometer. In the absence of inhibitors, DEPN-8 + 1.5% SP-B/C and CLSE rapidly reached minimum surface tensions <1 mN/m (0.5 and 2.5 mg surfactant phospholipid/ml). DEPN-8 + 1.5% SP-B/C maintained its high surface activity in the presence of PLA2, while the surface activity of CLSE was significantly inhibited by exposure to this enzyme. DEPN-8 + 1.5% SP-B/C also had greater surface activity than CLSE in the presence of LPC, and the two surfactants had equivalent surface activity in the presence of albumin. DEPN-8 + 1.5% SP-B/C also had slightly greater surface activity than CLSE when exposed to peroxynitrite in pulsating bubble studies. These results support the potential of developing highly active and inhibition-resistant synthetic exogenous surfactants containing DEPN-8 + apoprotein/peptide constituents for use in treating direct pulmonary forms of clinical acute lung injury (ALI) and the acute respiratory distress syndrome (ARDS).







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