In the in vivo rat heart model with transient (5 min) regional ischemia, as induced by left coronary artery ligation, we have demonstrated that perezone reduces dramatically the incidence of reperfusion-induced-arrhythmias. Administered 5 minutes before coronary occlusion, at a dose of 3.1 mg/kg, this drug effectively protects against the high incidence of arrhythmias and the fall of blood pressure. In addition, it inhibits the release of lactic dehydrogenase and creatine-kinase enzymes to the plasma. We propose that the protective effect of perezone might be related to its well documented action of promoting the release of intramitochondrial Ca2+, thus, maintaining ATP production during reperfusion.
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HADASSAH UNIV HOSP, JOSEPH LUNENFELD CARDIAC SURG RES CTR, IL-91120 JERUSALEM, ISRAELHADASSAH UNIV HOSP, JOSEPH LUNENFELD CARDIAC SURG RES CTR, IL-91120 JERUSALEM, ISRAEL
AVRIEL, E
APPELBAUM, Y
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HADASSAH UNIV HOSP, JOSEPH LUNENFELD CARDIAC SURG RES CTR, IL-91120 JERUSALEM, ISRAELHADASSAH UNIV HOSP, JOSEPH LUNENFELD CARDIAC SURG RES CTR, IL-91120 JERUSALEM, ISRAEL
APPELBAUM, Y
URETZKY, G
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HADASSAH UNIV HOSP, JOSEPH LUNENFELD CARDIAC SURG RES CTR, IL-91120 JERUSALEM, ISRAELHADASSAH UNIV HOSP, JOSEPH LUNENFELD CARDIAC SURG RES CTR, IL-91120 JERUSALEM, ISRAEL