Attenuation of ischemia/reperfusion injury in rats by a caspase inhibitor

Background-Z-Val-Ala-Asp(OMe)-CH2F (ZVAD-fmk), a tripeptide inhibitor of the caspase interleukin-1 beta-converting enzyme family of cysteine protases, may reduce myocardial reperfusion injury in vivo by attenuating cardiomyocyte apoptosis within the ischemic area at risk. Methods and Results-Sprague-Dawley rats were subjected to a 30-minute coronary occlusion followed by a 24-hour reperfusion. An inert vehicle (dimethylsulfoxide; group 1, n = 8) or ZVAD-fmk, at a total dose of 3.3 mg/kg (group 2, n = 8), was administered intravenously every 6 hours starting at 30 minutes before coronary occlusion until 24 hours of reperfusion. At this 24-hour point, hemodynamics were assessed by means of cardiac catheterization; then, the rats were killed, and the left ventricle was excised and sliced. The myocardial infarct size/ischemic area at risk and the count of presumed apoptotic cardiomyocytes (terminal deoxynucleotidyl transferase-mediated dUTP-biotin nick end labeling [TUNEL]-positive cells) within the ischemic area at risk were assessed through triphenyltetrazolium chloride staining and TUNEL methods, respectively. Peak positive left ventricular dP/dt was higher (P = .02) and left ventricular end-diastolic pressure was lower (P = .04) in group 2 than in group 1. The infarct size/ischemic area at risk of group 2 (52.4 +/- 4.0%) was smaller (P = .02) than that of group 1 (66.6 +/- 3.7%), and TUNEL-positive cells were fewer (P = .0002) (group 2, 3.1 +/- 0.9%; group 1, 11.1 +/- 1.0%). Agarose gel electrophoresis revealed DNA laddering in the border zone myocardium of group 1, but DNA ladder formation was attenuated in group 2. Conclusions-ZVAD-fmk was effective in reducing myocardial reperfusion injury, which could at least be partially attributed to the attenuation of cardiomyocyte apoptosis.