Klein H H, Bohle R M, Pich S, Lindert-Heimberg S, Wollenweber J, Schade-Brittinger C, Nebendahl K
Med. Klinik II, Städt. Krankenanstalten Idar-Oberstein GmbH, Germany.
J Mol Cell Cardiol. 1998 Apr;30(4):795-801. doi: 10.1006/jmcc.1998.0644.
Inhibition of Na+/H+ exchange has been shown to protect the ischemic reperfused myocardium. This study investigated the time-dependent beneficial effect of the Na+/H+ exchange inhibitor HOE642 (4-isopropyl-3-methylsulphonylbenzoyl-guanedine methanesulphonite, cariporide). The left anterior descending coronary artery was ligated in 21 pigs (seven control animals) for 60 min and then reperfused for 24 h. An extracorporeal bypass system was used to achieve a constant residual blood flow of 3 ml/min within the ischemic myocardium. Cariporide (1 mg/kg) was injected intravenously in seven pigs after 15 min of ischemia (group A), and in another seven animals after 45 min of ischemia (group B). Histochemical (tetrazolium stain) and histologic infarct sizes were determined at the end of the experiments. Regional systolic shortening was determined by sonomicrometry. Mean calculated residual blood flows (ml/min/g of ischemic myocardium) amounted to 0.106 (group A), 0.093 (group B), and 0.117 (control group). Histochemical (32.9 +/- 21%) and histologic infarct sizes (36.7 +/- 17.7%) were significantly reduced in group A compared to both the control group (histochemical infarct size, 62.5 +/- 16.1%, P < 0.01; histologic infarct size. 67.8 +/- 16.3%, P = 0.013) and group B (histochemical infarct size 64.8 +/- 12.2%, P < 0.01; histologic infarct size 67.1 +/- 15.6%, P < 0.01). Infarct sizes of group B did not differ from control values. Recovery of regional systolic shortening after 24 h of reperfusion was insignificantly improved in group A compared to both other groups. In conclusion, inhibition of Na+/H+ exchange during early ischemia reduced cell death in an ischemic reperfused preparation with low residual blood flow.
已证实抑制钠氢交换可保护缺血再灌注心肌。本研究调查了钠氢交换抑制剂HOE642(4-异丙基-3-甲基磺酰基苯甲酰胍甲磺酸盐,卡里波罗)的时间依赖性有益作用。在21头猪(7头对照动物)中结扎左冠状动脉前降支60分钟,然后再灌注24小时。使用体外循环系统使缺血心肌内的残余血流量恒定为3毫升/分钟。7头猪在缺血15分钟后静脉注射卡里波罗(1毫克/千克)(A组),另外7头动物在缺血45分钟后注射(B组)。在实验结束时测定组织化学(四氮唑染色)和组织学梗死面积。通过声测法测定局部收缩期缩短。计算得出的平均残余血流量(毫升/分钟/克缺血心肌)在A组为0.106,B组为0.093,对照组为0.117。与对照组(组织化学梗死面积,62.5±16.1%,P<0.01;组织学梗死面积,67.8±16.3%,P = 0.013)和B组(组织化学梗死面积64.8±12.2%,P<0.01;组织学梗死面积67.1±15.6%,P<0.01)相比,A组的组织化学(32.9±21%)和组织学梗死面积(36.7±17.7%)显著减小。B组的梗死面积与对照值无差异。与其他两组相比,A组在再灌注24小时后局部收缩期缩短的恢复情况改善不明显。总之,在早期缺血期间抑制钠氢交换可减少低残余血流量的缺血再灌注标本中的细胞死亡。