Schoemaker R G, van Heijningen C L
Department of Pharmacology, Faculty of Medicine and Health Sciences, Erasmus University, NL-3000 DR Rotterdam, The Netherlands.
Am J Physiol Heart Circ Physiol. 2000 May;278(5):H1571-6. doi: 10.1152/ajpheart.2000.278.5.H1571.
Preconditioning the heart by brief coronary (CAO) or mesenteric artery occlusion (MAO) can protect against damage during subsequent prolonged CAO and reperfusion. The role of bradykinin (BK) in remote cardiac preconditioning by MAO is investigated by antagonizing the BK B(2) receptor [Hoechst 140 (HOE-140)] or simulating local BK release by mesenteric intra-arterial infusion. Anesthetized male Wistar rats (n = 6-8) were treated with HOE-140 or saline before starting the preconditioning protocol, CAO, MAO, or non-preconditioned control. Infarct size related to risk area [ratio of infarct area to area at risk (IA/AR)] was determined after 3 h of reperfusion following a 60-min CAO. IA/AR was 62 +/- 5% in controls and not affected by HOE-140 (58 +/- 6%). CAO as well as MAO significantly protected the heart (IA/AR, 37 +/- 3 and 35 +/- 5%), which was prevented by HOE-140 (IA/AR, 71 +/- 6 and 65 +/- 7%, respectively). Brief intramesenteric BK infusion mimicked MAO (IA/AR, 26 +/- 3%). Pretreatment with hexamethonium could abolish this protection (IA/AR, 67 +/- 4%). These data indicate an important role for BK in remote preconditioning by MAO. Results support the hypothesis that remote preconditioning acts through sensory nerve stimulation in the ischemic organ.
通过短暂冠状动脉闭塞(CAO)或肠系膜动脉闭塞(MAO)对心脏进行预处理,可以保护心脏在随后长时间的CAO和再灌注过程中免受损伤。通过拮抗缓激肽B(2)受体[赫斯特140(HOE - 140)]或通过肠系膜动脉内输注模拟局部缓激肽释放,研究缓激肽(BK)在MAO介导的远程心脏预处理中的作用。在开始预处理方案、CAO、MAO或非预处理对照之前,用HOE - 140或生理盐水处理麻醉的雄性Wistar大鼠(n = 6 - 8)。在60分钟CAO后再灌注3小时后,测定梗死面积与危险区域的关系[梗死面积与危险区域面积之比(IA/AR)]。对照组的IA/AR为62±5%,不受HOE - 140影响(58±6%)。CAO以及MAO均能显著保护心脏(IA/AR分别为37±3%和35±5%),而HOE - 140可阻止这种保护作用(IA/AR分别为71±6%和65±7%)。肠系膜内短暂输注BK可模拟MAO(IA/AR为26±3%)。六甲铵预处理可消除这种保护作用(IA/AR为67±4%)。这些数据表明BK在MAO介导的远程预处理中起重要作用。结果支持远程预处理通过缺血器官中的感觉神经刺激起作用这一假说。