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Eur J Cardiothorac Surg 2005;27:774-782
© 2005 Elsevier Science NL


Surfactant pretreatment ameliorates ischemia-reperfusion injury of the lung

Niels P. van der Kaaija,b,*, Jack J. Haitsmac, Jolanda Kluina, Bart N. Lambrechtd, Burkhard Lachmannc, Ron W.F. de Bruinb, Ad J.J.C. Bogersa

a Department of Cardio-Thoracic Surgery, Erasmus MC Rotterdam, Rotterdam, The Netherlands
b Department of Surgery, Erasmus MC Rotterdam, Rotterdam, The Netherlands
c Department of Anesthesiology, Erasmus MC Rotterdam, Rotterdam, The Netherlands
d Department of Pulmonary Diseases, Erasmus MC Rotterdam, Rotterdam, The Netherlands

Received 31 August 2004; received in revised form 17 December 2004; accepted 23 December 2004.

* Corresponding author. Address: Erasmus MC Rotterdam, Postbus 1738, 3000 DR Rotterdam, The Netherlands. Tel.: +31 10 4087693/624816437; fax: +31 10 4089471. (E-mail: n.vanderkaaij{at}erasmusmc.nl).

Objective: To investigate whether surfactant pretreatment provides lung protection in an animal model of lung ischemia-reperfusion injury (LIRI). Methods: Male Sprague–Dawley rats (n=100) were randomised to receive intratracheally administered surfactant or no pretreatment. One hour thereafter, animals underwent 120min of warm ischemia of the left lung, or were sham-operated. A third group served as healthy untreated controls. Animals were killed on day 1, 3 or 7. Blood gas values were measured and lung compliance was recorded. Broncho-alveolar lavage fluid (BALf) was obtained to assess the amount of alveolar protein, the ratio of small to large aggregate surfactant phospholipids (SA/LA ratio), and leukocyte infiltration (granulocytes, macrophages and lymphocytes, measured by Flow Cytometry). Results: LIRI resulted in a mortality rate of 17% and significantly decreased lung compliance and PaO2 (day 1 and 3 P<0.001, day 7 P<0.05) as compared to sham-operated and healthy controls. On day 1 more protein was present in the alveoli of ischemic lungs (P<0.001) than in sham-operated and healthy controls. Furthermore, LIRI resulted in an increased SA/LA ratio in the left lung on day 1 (P<0.05) and caused infiltration of granulocytes (day 1, 3 and 7 (P<0.01)), macrophages (day 3 (P<0.05) and 7 (P<0.01) and lymphocytes (day 3 and 7 (P<0.01)) in the BALf as compared to sham-operated and healthy controls. Surfactant pretreatment improved survival, lung compliance (day 3 P<0.001) and PaO2 (day 1, 3 (P<0.01 and 7 (P<0.05)). It also reduced protein leakage (P<0.05) and prevented an increase in the SA/LA ratio (P<0.01). Although the number of macrophages and granulocytes in the BALF was increased on day 1 and 3 (P<0.01) after surfactant pretreatment as compared to all other groups, the number of lymphocytes was reduced on day 3 (P<0.05). Conclusions: The present study shows that surfactant pretreatment enhances recovery of lung function and lung mechanics after LIRI, resulting in normal parameters from day 3 onwards. Surfactant pretreatment in this LIRI model may provide useful information to improve donor lung function after lung transplantation.

Key Words: Ischemia-reperfusion injury • Lung • Pulmonary surfactant • Animal models




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