摘要
This is a report of a study on the protective effect of berberine(Ber) on postischemic myocardial stunning and the role it plays in ATPase activity. Isolated working rat hearts were used with global ischemia for 30 min followed by reperfusing for 40 min. Both systolic and diastolic functions of stunned myocardium were significantly decreased. The recovery of LVSP×HR and CO was 52%±8% and 40%±8% respectively; LVEDP and T were elevated; while both Na +, K +ATPase activity and Ca 2+ , Mg 2+ ATPase activity of myocardial membrane and mitochondria were depressed. Berberine(25 mg·kg -1 ·d -1 , ip, 3 d, and 10 μmol L -1 for isolated heart perfusion) was able to enhance the percent recovery of LVSP×HR and CO to 85%±12% and 75%±11%, respectively, and reduce LVEDP from 298%±64% to 166%±44%, with an improvement in myocardial membrane Na +, K +ATPase activity and mitochondria Ca 2+ , Mg 2+ ATPase activity. This study suggested that berberine can protect cardiac function from ischemia reperfusion stunning injury by preserving ATPase activity in ischemic myocardium.
This is a report of a study on the protective effect of berberine(Ber) on postischemic myocardial stunning and the role it plays in ATPase activity. Isolated working rat hearts were used with global ischemia for 30 min followed by reperfusing for 40 min. Both systolic and diastolic functions of stunned myocardium were significantly decreased. The recovery of LVSP×HR and CO was 52%±8% and 40%±8% respectively; LVEDP and T were elevated; while both Na +, K +ATPase activity and Ca 2+ , Mg 2+ ATPase activity of myocardial membrane and mitochondria were depressed. Berberine(25 mg·kg -1 ·d -1 , ip, 3 d, and 10 μmol L -1 for isolated heart perfusion) was able to enhance the percent recovery of LVSP×HR and CO to 85%±12% and 75%±11%, respectively, and reduce LVEDP from 298%±64% to 166%±44%, with an improvement in myocardial membrane Na +, K +ATPase activity and mitochondria Ca 2+ , Mg 2+ ATPase activity. This study suggested that berberine can protect cardiac function from ischemia reperfusion stunning injury by preserving ATPase activity in ischemic myocardium.
