Sharma A, Singh M
Department of Pharmaceutical Sciences and Drug Research, Punjabi University, Patiala, India.
Methods Find Exp Clin Pharmacol. 1997 Sep;19(7):493-9.
The role of adrenergic mechanism in the cardioprotective effect of ischemic preconditioning against ischemia-reperfusion induced injury in in vivo dog heart and isolated rat heart was investigated. Anesthetized dogs were subjected to LAD coronary artery ligation for 60 min followed by reperfusion for 4 h. Preconditioning protocol was 5 min of ischemia followed by reperfusion for 10 min. Rat hearts were subjected to global ischemia for 30 min followed by reperfusion for 30 min. Preconditioning protocol was 5 min global ischemia followed by reperfusion for 5 min repeated four times. Infarct size, electrocardiographic changes and release of LDH were estimated to assess the extent of cardiac injury. Preconditioning reduced the infarct size, ST segment elevation and prevented the loss of R wave. Prazosin attenuated the cardioprotective effect of preconditioning in dog. Preconditioning conferred protection against ischemia-reperfusion induced cardiac injury and reperfusion-induced arrhythmias in isolated rat heart. Reserpine pretreatment attenuated this protective effect of preconditioning on reperfusion-induced arrhythmias. These observations suggest the involvement of adrenergic mechanism in the cardioprotective and antiarrhythmic effect of ischemic preconditioning in dog and rat species respectively.
研究了肾上腺素能机制在缺血预处理对体内犬心脏和离体大鼠心脏缺血再灌注损伤的心脏保护作用中的作用。将麻醉的犬进行左冠状动脉前降支结扎60分钟,然后再灌注4小时。预处理方案为缺血5分钟,然后再灌注10分钟。大鼠心脏进行全心缺血30分钟,然后再灌注30分钟。预处理方案为全心缺血5分钟,然后再灌注5分钟,重复4次。通过评估梗死面积、心电图变化和乳酸脱氢酶释放来评估心脏损伤程度。预处理减小了梗死面积,降低了ST段抬高,并防止了R波丢失。哌唑嗪减弱了预处理对犬的心脏保护作用。预处理对离体大鼠心脏的缺血再灌注诱导的心脏损伤和再灌注诱导的心律失常具有保护作用。利血平预处理减弱了预处理对再灌注诱导的心律失常的这种保护作用。这些观察结果表明,肾上腺素能机制分别参与了犬和大鼠缺血预处理的心脏保护和抗心律失常作用。