This study was designed to assess the cardioprotective effect of
isosteviol on rats with heart
ischemia-reperfusion (IR) injury and to explore the mechanism of action of the compound. Sprague Dawley rats were divided into 8 groups (n=10-12): a
sham-operated control and 7
ischemia-reperfusion groups (IR control, 3
isosteviol pre-treated (0.5, 1.0 and 2.0 mg kg(-1)),
ligustrazine pre-treated, 5-hydroxydecanoate (5-HD) pre-treated and 5-HD+
isosteviol pre-treated groups). IR was produced by occluding the left coronary artery for 30 min followed by re-opening the artery for 90 min. The compounds under investigation were administered intravenously 10 min prior to occluding the artery. Hemodynamic parameters (+/-dp/dt(max), LVSP, LVDevP, MAP), heart rate,
ventricular tachycardia (VT) and
ventricular fibrillation (VF) were determined during the IR period. The
myocardial infarct size, activities of serum
lactate dehydrogenase and
creatine kinase were determined at the end of the experiment. In the
isosteviol pre-treated groups, the hemodynamic parameters were improved and the
myocardial infarct size, the activities of serum
enzymes, and the incidences of VT and VF were all decreased when compared to the control group. These effects of
isosteviol were similar to that of a traditional
cardioprotective agent,
ligustrazine. The 5-HD+
isosteviol group displayed parameters that were between those in the equivalent
isosteviol pre-treated group and the IR control group. In conclusion, damage due to a standard rat heart IR injury was reduced by pretreatment with intravenous
isosteviol, and this effect was partly attenuated by a mitochondrial
ATP-sensitive potassium channel blocker, 5-HD.