Propofol, a rapidly acting, short duration, intravenous
hypnotic anesthetic induction agent, is often used in clinical situations where
myocardial ischemia/ reperfusion (I/R) injury is a threat. The aim of the present study was to evaluate the protective effect of
propofol on myocardial I/R injury in rat due to apoptosis. Myocardial I/R injury were induced by occluding the left anterior descending (LAD) coronary artery for 25 min followed by either 2 h or 6 h reperfusion. Apoptosis was evaluated by Western blot analysis (Bcl-2, Bax expression),
DNA strand breaks, TUNEL analysis and measuring myocardial
caspase-3 activity.
Propofol significantly reduced
infarct size and improved I/R-induced myocardial contractile dysfunction by improving left ventricular diastolic pressure and positive and negative maximal values of the first derivative (+dp/dt) of left ventricular pressure.
Propofol increased Bcl-2/Bax expression ratio and decreased
caspase-3 activity in I/R rat hearts, which resulted in reduction of myocardial apoptosis as evidenced by TUNEL analysis and
DNA laddering experiments. In an in vitro study,
propofol increased H9c2 cell viability against oxidative stress induced by
glucose oxidase (GOX) in a dose-dependent manner. These data suggest
propofol limits I/R injury with an associated reduction in apoptotic cell death in vivo.