Procedure-induced inflammation and endothelial cell activation in an artificially ventilated and circulated porcine double-lung model.

Systemic inflammation is induced during extracorporeal circulation, resulting in an increased bleeding tendency and endothelial cell activation. Lungs from seven piglets were perfused by autologous blood in an extracorporeal circuit, where the lungs and the left atrium were attached to polyvinyl chloride (PVC) tubings and the blood circulated by a roller pump. The trachea was intubated and attached to a ventilator. The lungs maintained good gas exchange, despite a slight increase in lactate levels. Plasma tPA increased slightly over time, suggesting endothelial cell activation. Activation of inflammatory systems was reflected in increased levels of plasma interleukin (IL)-6 and IL-10. A model for the study of lung endothelial activation during extracorporeal circulation has been shown to be reproducible. The lung tissue was shown to be capable of gas exchange and activation of endothelial cells and procedure-induced inflammation were noted.

[1]  H. Schubert,et al.  Evaluation of isolated lung perfusion as neoadjuvant therapy of lung metastases using a novel in vivo pig model: I. Influence of perfusion pressure and hyperthermia on functional and morphological lung integrity. , 2004, European journal of cardio-thoracic surgery : official journal of the European Association for Cardio-thoracic Surgery.

[2]  C. Jern,et al.  Pulmonary net release of tissue‐type plasminogen activator during porcine primary and secondary acute lung injury , 2004, Acta anaesthesiologica Scandinavica.

[3]  S. Brister,et al.  Coagulation disorders of cardiopulmonary bypass: a review , 2004, Intensive Care Medicine.

[4]  C. Tchervenkov,et al.  Timing of steroid treatment is important for cerebral protection during cardiopulmonary bypass and circulatory arrest: minimal protection of pump prime methylprednisolone. , 2003, European journal of cardio-thoracic surgery : official journal of the European Association for Cardio-thoracic Surgery.

[5]  W. Mcbride,et al.  The effect of methylprednisolone on cytokine concentration and leukocyte adhesion molecule expression in an isolated cardiopulmonary bypass system. , 2003, Cytokine.

[6]  V. Hjortdal,et al.  Plasma cytokines do not reflect expression of pro‐ and anti‐inflammatory cytokine mRNA at organ level after cardiopulmonary bypass in neonatal pigs * , 2003, Acta anaesthesiologica Scandinavica.

[7]  B. Baudet,et al.  Pulmonary vascular endothelial growth factor and nitric oxide interaction during total cardiopulmonary bypass in neonatal pigs. , 2003, The Journal of thoracic and cardiovascular surgery.

[8]  S. Keshavjee,et al.  Ischemia-reperfusion-induced lung injury. , 2003, American journal of respiratory and critical care medicine.

[9]  K. Laczika,et al.  Endothelial cell activation and blood coagulation in critically ill patients with lung injury. , 2002, Wiener Klinische Wochenschrift.

[10]  John G. Laffey,et al.  The Systemic Inflammatory Response to Cardiac Surgery: Implications for the Anesthesiologist , 2002, Anesthesiology.

[11]  K. Messmer,et al.  Tissue Damage Of Non-Heart-Beating Donor Lungs After Long-Term Preservation: Evaluation of Histologic Alteration, Bronchoalveolar Lavage, and Energy Metabolism , 2002, Shock.

[12]  T. Yau,et al.  Cardiopulmonary bypass induced inflammation: pathophysiology and treatment. An update. , 2002, European journal of cardio-thoracic surgery : official journal of the European Association for Cardio-thoracic Surgery.

[13]  V. Brix-Christensen The systemic inflammatory response after cardiac surgery with cardiopulmonary bypass in children , 2001, Acta anaesthesiologica Scandinavica.

[14]  I. Cheifetz,et al.  Liquid lung ventilation reduces neutrophil sequestration in a neonatal swine model of cardiopulmonary bypass , 2001, Critical care medicine.

[15]  C. Jern,et al.  Surgical stress induces acute coronary release of tissue‐type plasminogen activator in the pig , 2000, Acta anaesthesiologica Scandinavica.

[16]  K. Mellgren,et al.  Influence of hemofiltration on plasma cytokine levels and platelet activation during extra corporeal membrane oxygenation. , 2000, Scandinavian Cardiovascular Journal.

[17]  Spiridon Cristina Monica,et al.  Vascular endothelium viability and function after total cardiopulmonary bypass in neonatal piglets. , 1999, American journal of respiratory and critical care medicine.

[18]  S. Bolling,et al.  Regulatory effects of interleukin-10 on lung ischemia-reperfusion injury. , 1996, The Journal of thoracic and cardiovascular surgery.

[19]  A Haverich,et al.  Systemic inflammatory response syndrome after cardiac operations. , 1996, The Annals of thoracic surgery.

[20]  K. Satoh,et al.  Hemodynamic forces modulate the effects of cytokines on fibrinolytic activity of endothelial cells. , 1996, Blood.

[21]  J. Lunec,et al.  Changes in “Inflammatory” Mediators and Total Body Water during Extra-Corporeal Membrane Oxygenation (ECMO). A Preliminary Study , 1995, The International journal of artificial organs.

[22]  T. Hedner,et al.  Blood Platelet Activation and Membrane Glycoprotein Changes during Extracorporeal Life Support (Ecls). In Vitro Studies , 1995, The International journal of artificial organs.

[23]  B. Smith,et al.  Platelet-leukocyte activation and modulation of adhesion receptors in pediatric patients with congenital heart disease undergoing cardiopulmonary bypass. , 1994, The Journal of thoracic and cardiovascular surgery.

[24]  D. Taggart,et al.  Respiratory dysfunction after uncomplicated cardiopulmonary bypass. , 1993, The Annals of thoracic surgery.

[25]  S. Westaby,et al.  Cytokine responses to cardiopulmonary bypass with membrane and bubble oxygenation. , 1992, The Annals of thoracic surgery.