Download PDF
Thorac Cardiovasc Surg 1985; 33(6): 354-359
DOI: 10.1055/s-2007-1014167
© Georg Thieme Verlag Stuttgart · New York

Calcium Antagonists and Myocardial Protection: A Comparative Study of the Functional, Metabolie and Electrical Consequences of Verapamil and Nifedipine as Additives to the St. Thomas' Cardioplegic Solution*

F. Yamamoto1 , A. S. Manning, R. Crome, M. V. Braimbridge, D. J. Hearse
  • The Heart Research Unit, The Rayne Institute, St. Thomas' Hospital, London, UK
  • 1Kleinwort Fellow in Cardiothoracic Surgery. Present address: National Cardiovascular Center, Suita Osaka, Japan
*This work was supported in part by grants from the British Heart Foundation and St. Thomas' Hospital Research Endowments Fund
Further Information

Publication History

1985

Publication Date:
19 March 2008 (online)

  PDF Download  Permissions and Reprints All articles of this category

Summary

Using an isolated rat heart preparation as a model of cardiopulmonary bypass and ischemic arrest, a comparative study has been undertaken in Order to characterize the functional, metabolic and electrophysiological consequences resulting from the addition of dlverapamil or nifedipine to the St. Thomas' Hospital cardioplegic Solution. Hearts (n = 6 in each group) were subjeeted to cardioplegic infusion with the St. Thomas' Solution with or without added Verapamil (1.1 micromoles/liter) or nifedipine (0.075 micromoles/liter). After 35 minutes of normothermic (37 °C) ischemic arrest, reperfusion was initiated and functional recovery was measured and expressed as a percent of its pre-ischemic control value. Inclusion of nifedipine in the cardioplegic Solution improved the post-ischemic recovery of cardiac Output from its control value of 59.8 ± 3.0 % to 80.0 ± 2.5 %. The temporal characteristics for the post-ischemic recovery of electrical activity and contractile Performance were uncomplicated and similar to control hearts. Inclusion of Verapamil also improved the protective properties of the St. Thomas' Solution with cardiac Output recovering to 76.8 % ± 2.8 %. However, in contrast to the control and nifedipine groups, the profile for functional recovery was complex. After an early initial recovery, pressure development declined for 0.5 to 6.0 minutes. This oecurred despite the recovery of electrical activity. Hearts then exhibited a second phase of recovery where pressure development returned to normal and this was sustained for the duration of the experiment. Analysis of electrocardiographic characteristics revealed a significant Prolongation of the P-P and P-Q interval during the first 10 minutes of reperfusion in the Verapamil group. No significant changes oecurred in the control and nifedipine groups. No significant differences in the recovery of ATP or CP oecurred between the groups. In conclusion, despite a similar ability to protect the myocardium against global ischemia, nifedipine and Verapamil exhibit significant differences in mode and characteristics of recovery during early reperfusion.

Key words

Calcium antagonists - Cardioplegia - Myocardial protection - Reperfusion arrhythmias - Electromechanical dissociation

      >