Long-term magnetic resonance imaging/spectroscopy study of cariporide in a canine cardiac ischemia/reperfusion model.

Abstract

Using both 31P and 1H cardiac magnetic resonance techniques, it is possible to monitor the functional (ejection fraction [EF]) and biochemical (pH) status of the heart following a reperfused ischemic insult. This study assessed the effects of Na+/H+ exchange inhibition with cariporide in a closed-chest canine ischemia/reperfusion model. Dogs received 1-mg/kg cariporide treatments for 3 days after occlusion, but were monitored for 10 days. Baseline intracellular pH (+/-SEM) for the control and treated groups were 7.10 +/- 0.03 and 7.14 +/- 0.04, respectively, and dropped to 6.25 +/- 0.08 and 6.38 +/- 0.08 during occlusion. There was a significant increase in pH from occlusion to early reperfusion in the control group (P = 0.03) but, during the same time period, this increase was not seen in the cariporide group. There was a significant (P = 0.01) drug interaction in recovery of EF over the 10-day protocol. Individual time-point analysis revealed significant differences at immediate reperfusion through day 3 (73.9% +/- 2.5%, 84.5% +/- 3.1%; baseline normalized EF controls and cariporide, respectively). Neither pH nor EF measurements were significantly different between the groups at day 10. Despite early functional and metabolic benefits, infarct size, as measured at day 10, was 13.2% +/- 2.2% for the controls and 11.8% +/- 2.3% for the cariporide group (NS). Thus there were no long-term cariporide functional or biochemical benefits.

• Authors: Kerry Thompson, Robert Terry Thompson, Jane Sykes, Gerald Wisenberg
• Journal: Journal of cardiovascular pharmacology (J Cardiovasc Pharmacol) Vol. 41 Issue 4 Pg. 536-43 (Apr 2003) ISSN: 0160-2446 [Print] United States
• PMID: 12658054 (Publication Type: Comparative Study, Journal Article, Research Support, Non-U.S. Gov't)

Chemical References

• Guanidines
• Sulfones
• cariporide

Topics

• Animals
• Disease Models, Animal
• Dogs
• Female
• Guanidines (pharmacokinetics, pharmacology, therapeutic use)
• Hemodynamics (drug effects, physiology)
• Magnetic Resonance Imaging (methods)
• Magnetic Resonance Spectroscopy (methods)
• Myocardial Reperfusion Injury (drug therapy, metabolism)
• Sulfones (pharmacokinetics, pharmacology, therapeutic use)