ABSTRACT
To investigate the effects of acetazolamide on the ischemia-reperfused isolated hearts of 2- and 8-week-old rabbits. This study was conducted at the Kermanshah Medical Biology Research Center, Kermanshah, Iran from March to September 2011. Two- [n=17] and 8-week old [n=17] rabbits were separately divided into 2 control [n=9], and test [n=8] groups. Isolated hearts were subjected to 35 minutes ischemia and 30 minutes reperfusion. Acetazolamide [100 microgr/l] was added to the perfusion solution for 10 minutes before ischemia in the test group. Cardiac parameters including ventricular pressure, heart rate [HR], and rate pressure product [RPP] were measured. Data sets were analyzed by t-test. Following acetazolamide administration the change percentage of HR was significantly different in the 2-week [91 +/- 1.1%] compared with the 8- week [96 +/- 0.8%] test groups [p=0.0016]. Recovery percentage of RPP in reperfusion was lower [p=0.005] in the 8- [28.9 +/- 3.4%] than the 2-week test groups [45.2 +/- 3.5%]. The 2-week hearts elicited more rapid response to carbonic anhydrase [CA] inhibition than the 8-week group. However, acetazolamide does not exacerbate ischemia-reperfusion [I/R] injury in the 2-week hearts. Therefore, it was revealed that after inhibition of CA, the age dependent pattern of I/ R injury was similar to that of the normal hearts. Inspite of the CA important role in the normal heart function, it is not a determining factor in I/R injury in different ages
ABSTRACT
To evaluate whether repeated diazepam administration affects the heart in ischemia- reperfusion. This study was performed at the Medical Biology Research Center, Kermanshah, Iran, from March to September 2008. Four groups of rats were subjected to a daily injection of diazepam [group 1 [0.5 mg/kg for 21 days], group II [2.5 mg/kg for 5 days], and group III [5 mg/kg for 5 days] intraperitoneally], and saline solution [21 days] in the control groups. Isolated, perfused hearts were subjected to 40 minutes global ischemia, and 45 minutes reperfusion. The left ventricular developed pressure [LVDP], heart rate, and coronary flow were measured. Rate pressure product [RPP] was calculated. In reperfusion, released lactate dehydrogenase [LDH] enzyme in effluent was measured. It was observed that the recovery of the RPP and LVDP in reperfusion significantly decreased in the test group III [n=9] in comparison to the control [n=8]. During the reperfusion period, the released LDH significantly increased in test group II [n=8] and group III in comparison with the control. The results show that repeated administration of diazepam [5 mg/kg for 5 days] reduced the cardiac performance in reperfusion, and significantly exacerbated the ischemia-reperfusion injury. It is probably mediated by the changing of cardiac susceptibility in ischemia due to repeated administration of diazepam
Subject(s)
Male , Animals, Laboratory , Heart/drug effects , Myocardium , Myocardial Reperfusion Injury/drug therapy , Myocardial Reperfusion , Rats, WistarABSTRACT
To investigate the effects of cardio depressant concentration of diazepam on the function of isolated rat heart in ischemia-reperfusion. This study was performed at the Medical Biology Research Center, Kermanshah, Iran from November 2006 to March 2007. Isolated, perfused rat hearts were subjected to 40 minutes normothermic global ischemia and 45 minutes reperfusion. Diazepam 100 micro molar was added to the perfusion solution for 10 minutes before ischemia in the test group. Different cardiac variables including left ventricular developed pressure, heart rate, and coronary flow CF were measured. Rate pressure product RPP was calculated, during the ischemic period time until onset of ischemic contracture and maximum contracture were determined. In reperfusion, released lactate dehydrogenase enzyme in effluent was measured and cardiac functional recovery was determined. It was found that diazepam significantly decreased RPP and increased CF before ischemia. In the diazepam group n=10, during ischemia, maximum contracture was significantly lower than the control group n=14. Also, diazepam significantly increased functional recovery and coronary flow in reperfusion. Diazepam 100 micro molar significantly decreased maximum contracture during ischemia, improved the recovery of myocardial function and CF in reperfusion. The results show that the cardio depressant concentration of diazepam is safe and relatively protective in the ischemia-reperfused isolated rat heart. These effects may be mediated by inhibition of calcium current in cardiomyocytes