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Evaluation of alveolar surfactant aggregates in vitro and in vivo

Dept of Physiology and Medicine, Lawson Health Research Institute, The University of Western Ontario, London, Ontario, Canada

CORRESPONDENCE: A.M. Brackenbury, Lawson Health Research Institute, Room H417, St. Joseph's Health Centre, 268 Grosvenor Street, London, ON, Canada, N6A 4V2. Fax: 1 5196466110

Keywords: Acute respiratory distress syndrome, large aggregates, lavage model, pulmonary surfactant, small aggregates

Received: February 1, 2001
Accepted July 25, 2001

In acute lung injury, a decrease in surface-active large aggregates and an increase in the less surface-active small surfactant aggregates are observed. The objective of the current study was to determine if the increase in small aggregates interfered with the function of large aggregates, thereby independently contributing to lung dysfunction.

Isolated large aggregates, small aggregates, and large aggregate+small aggregate combinations were analysed for in vitro surface activity utilizing a pulsating bubble surfactometer. Subsequently, large aggregates, small aggregates, and large aggregate+small aggregate combinations were administered to surfactant-deficient, adult Sprague-Dawley rats. Physiological parameters were measured during 1 h of ventilation. After sacrifice, the whole lung lavage was analysed for protein concentration, and surface activity of the recovered large aggregates.

The minimum surface tension of the large aggregate+small aggregate preparations (10 mN·m^–1) was significantly higher than large aggregates alone (1 mN·m^–1), but lower than small aggregates alone (21 mN·m^–1) after 100 pulsations. In vivo, rats receiving large aggregates+small aggregates showed immediate increases in oxygenation, similar to animals given large aggregates, whereas animals given small aggregates and control animals maintained low oxygenation values.

In conclusion, small aggregates interfered with large aggregates function in vitro, but this was not observed in vivo in this experimental model.