Cardiopulmonary bypass reduces atrial Na+-K+-ATPase expression in children

Mladen Pavlovic1, André Schaller, Roland A Ammann

  • 1Division of Pediatric Cardiology, Department of Pediatrics, University Hospital, 3010 Berne, Switzerland. mladen.pavlovic@insel.ch

Insights

Cardiopulmonary bypass (CPB) impacts myocardial function by reducing Na(+)-K(+)-ATPase in children with left-to-right shunts. This molecular change occurs early and highlights the importance of underlying heart defects in CPB susceptibility.

Area of Science:

  • Pediatric Cardiology
  • Molecular Cardiology
  • Cardiovascular Surgery

Background:

  • Cardiopulmonary bypass (CPB) can cause myocardial dysfunction.
  • The sodium-potassium adenosine triphosphatase (Na(+)-K(+)-ATPase) is crucial for heart muscle function.
  • Developmental regulation of Na(+)-K(+)-ATPase necessitates pediatric-specific research.

Purpose of the Study:

  • To investigate the impact of CPB on Na(+)-K(+)-ATPase expression in pediatric patients.
  • To determine if underlying heart defects influence susceptibility to CPB-induced molecular changes.

Main Methods:

  • Myocardial tissue samples were collected from pediatric patients undergoing heart surgery before and after CPB.
  • Patients were categorized into groups with (VO) and without (NO) left-to-right shunts at the atrial level.
  • Expression levels of Na(+)-K(+)-ATPase isoforms were analyzed using molecular techniques.

Main Results:

  • CPB significantly decreased the expression of Na(+)-K(+)-ATPase isoforms ATP1A1 and ATP1A3.
  • This reduction in Na(+)-K(+)-ATPase expression was exclusively observed in the group with left-to-right atrial shunts (VO).
  • No patients exhibited clinical heart failure before or after surgery, suggesting an early molecular event.

Conclusions:

  • Underlying left-to-right atrial shunts increase susceptibility to CPB-induced alterations in Na(+)-K(+)-ATPase expression.
  • Reduced Na(+)-K(+)-ATPase mRNA expression appears to be an early molecular consequence of CPB in vulnerable pediatric patients.
  • These findings underscore the importance of considering congenital heart defects when assessing CPB risks in children.

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