Thorac Cardiovasc Surg 2010; 58(2): 86-92
DOI: 10.1055/s-0029-1186271
Original Cardiovascular

© Georg Thieme Verlag KG Stuttgart · New York

Efficacy of the Non-Adenosine Analogue A1 Adenosine Receptor Agonist (BR-4935) on Cardiovascular Function after Cardiopulmonary Bypass

G. Veres1 , 4 [*] , T. Radovits1 [*] , G. Otila1 , K. Hirschberg1 , 4 , H. Haider1 , N. Krieger1 , A. Knoll2 , E. Weigang3 , Z. Szabolcs4 , M. Karck1 , G. Szabó1
  • 1Department of Cardiac Surgery, University of Heidelberg, Heidelberg, Germany
  • 2Bayer HealthCare, Wuppertal, Germany
  • 3Department of Cardiovascular Surgery, University of Freiburg, Freiburg, Germany
  • 4Department of Cardiovascular Surgery, Semmelweis University, Budapest, Hungary
Further Information

Publication History

received February 1, 2009

Publication Date:
23 March 2010 (online)

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Abstract

Background: We tested the hypothesis that pharmacological preconditioning with a newly developed, potent non-adenosine analogue A1AdoR agonist (BR-4935) improves biventricular cardiac and endothelial function after cardiopulmonary bypass. Methods: Twelve anesthetized dogs underwent cardiopulmonary bypass. Dogs were divided into two groups: group 1 (n = 6) received saline vehicle, group 2 (n = 6) received BR-4935 before cardiopulmonary bypass. Biventricular hemodynamic variables were measured using a combined pressure-volume conductance catheter. Coronary blood flow, ATP content, malondialdehyde and myeloperoxidase levels and vasodilatative responses to acetylcholine and sodium nitroprusside were also determined. Results: Administration of the A1AdoR agonist led to a significantly better recovery of left and right ventricular systolic function after 60 minutes of reperfusion. Although the vasodilatative response to sodium nitroprusside was similar in both groups, acetylcholine resulted in a significantly greater increase in coronary blood flow in the BR-4935 group. In addition, the ATP content was significantly higher in the same group. Furthermore, malondialdehyde and myeloperoxidase levels significantly decreased in the A1AdoR group. Conclusion: Pharmacological preconditioning with a new, potent non-adenosine analogue A1AdoR agonist improves biventricular function recovery and endothelial function after hypothermic cardiac arrest.

References

1 These authors contributed equally to this work.

Gábor Veres, MD

Department of Cardiac Surgery
University of Heidelberg

INF 326

69120 Heidelberg

Germany

Phone: + 49 62 21 56 62 46

Fax: + 49 62 21 56 45 71

Email: gaborveres@yahoo.com