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J Thorac Cardiovasc Surg 2007;134:74-81
© 2007 The American Association for Thoracic Surgery
Surgery for Congenital Heart Disease |
a Division of Cardiovascular Surgery, Toronto General Hospital, University of Toronto, Toronto, Canada
b Division of Cardiology, Toronto General Hospital, University of Toronto, Toronto, Canada
c Hospital for Sick Children, Richard Lewar Centre of Excellence, Toronto General Hospital, University of Toronto, Toronto, Canada.
Received for publication June 13, 2006; revisions received January 2, 2007; accepted for publication January 8, 2007. * Address for reprints: Dr John G. Coles, Division of Cardiovascular Surgery, Hospital for Sick Children, 555 University Avenue, Toronto, M5G 1X8, Canada. (Email: john.coles{at}sickkids.ca).
Objective: The effects of cold cardioplegic arrest and reperfusion on human ventricular gene expression are unknown. We tested the hypothesis that intraoperative ischemia-reperfusion under conditions of blood cardioplegic arrest would induce a unique myocardial genomic profile indicative of a cardioprotective response.
Methods: Right ventricular samples were serially acquired during surgical repair of ventricular septal defect.
Results: Expression profiling revealed 3 patterns of gene expression: (1) increased expression above control levels within 1 hour of cardioplegic arrest, with further amplification during early reperfusion; (2) increased expression limited to the reperfusion phase; and (3) reduced expression during reperfusion. Functional annotation and network mapping of differentially expressed genes indicated activation of multiple signaling pathways regulated by phosphatidylinositide 3'-OH kinase convergent on cellular growth and reparative programs. Also observed was increased expression of genes regulating hemoglobin synthesis, suggesting a novel cardioprotective pathway evoked during ischemia-reperfusion.
Conclusion: Reversible myocardial ischemia-reperfusion during cardiac surgery is associated with an immediate genomic response that predicts a net cardioprotective phenotype.
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