Mitrev Z, Beyersdorf F, Hallmann R, Poloczek Y, Ihnken K, Herold H, Unkelbach U, Zimmer G, Freisleben H J, Satter P
Department of Thoracic and Cardiovascular Surgery, Johann Wolfgang Goethe-University, Frankfurt am Main, Germany.
Cardiovasc Surg. 1994 Dec;2(6):737-48.
Previous studies in isolated limbs using crystalloid perfusion solutions have shown that control of the initial reperfusion reduces postischaemic complications. However, no experimental study has been undertaken to evaluate the concept of controlled limb reperfusion experimentally in an in vivo blood-perfused model and to assess the local as well as systemic effects of normal blood reperfusion and controlled limb reperfusion. Of 20 pigs undergoing preparation of the infrarenal aorta and iliac arteries, six were observed for 7.5 h and served as controls; 14 others underwent 6 h of complete infrarenal occlusion. Thereafter, embolectomy was simulated in eight pigs by removing the aortic clamp and establishing normal blood reperfusion at systemic pressure. In six other pigs, the composition of the reperfusate and the conditions of reperfusion were controlled during the first 30 min, followed by normal blood reperfusion. Some 6 h of infrarenal aortic occlusion leads to a severe decrease in high-energy phosphates and muscle temperature, together with a slight increase in creatine kinase and potassium in the systemic circulation. Normal blood reperfusion resulted in severe reperfusion injury: massive oedema developed, the tissue showed a marked decrease in oxygen consumption, glucose consumption, tissue ATP, total adenine nucleotides, muscle pH and total calcium in the femoral vein. Furthermore, a massive increase was seen in plasma creatine kinase concentration and potassium, together with the development of muscle rigidity. In sharp contrast, initial treatment of the ischaemic skeletal muscle by controlled limb reperfusion resulted in normal water content, oxygen consumption, glucose consumption, flow and muscle rigidity. Furthermore, controlled limb reperfusion resulted in higher total adenine nucleotides content, less tissue acidosis, markedly reduced creatine kinase release, and potassium release as compared with that of normal blood reperfusion. This study shows that 6 h of acute infrarenal aortic occlusion will result in severe reperfusion injury (postischaemic syndrome) if normal blood at systemic pressure is given in the initial reperfusion phase. In contrast, initial treatment of the ischaemic skeletal muscle by controlled limb reperfusion reduces the metabolic, functional and biochemical alterations.
以往在离体肢体上使用晶体灌注液的研究表明,控制初始再灌注可减少缺血后并发症。然而,尚未有实验研究在体内血液灌注模型中对控制性肢体再灌注的概念进行实验评估,也未评估正常血液再灌注和控制性肢体再灌注的局部及全身影响。在20只接受肾下腹主动脉和髂动脉制备的猪中,6只观察7.5小时作为对照;另外14只接受6小时的完全肾下闭塞。此后,8只猪通过移除主动脉夹并在体循环压力下建立正常血液再灌注来模拟栓子切除术。在另外6只猪中,在最初30分钟内控制再灌注液的成分和再灌注条件,随后进行正常血液再灌注。约6小时的肾下主动脉闭塞会导致高能磷酸盐和肌肉温度严重降低,同时体循环中的肌酸激酶和钾略有升高。正常血液再灌注导致严重的再灌注损伤:出现大量水肿,组织的氧消耗、葡萄糖消耗、组织三磷酸腺苷(ATP)、总腺嘌呤核苷酸、肌肉pH值和股静脉总钙显著降低。此外,血浆肌酸激酶浓度和钾大量增加,同时出现肌肉僵硬。与之形成鲜明对比的是,通过控制性肢体再灌注对缺血骨骼肌进行初始治疗可使水分含量、氧消耗、葡萄糖消耗、血流和肌肉僵硬恢复正常。此外,与正常血液再灌注相比,控制性肢体再灌注导致总腺嘌呤核苷酸含量更高、组织酸中毒减轻、肌酸激酶释放和钾释放明显减少。本研究表明,如果在初始再灌注阶段给予体循环压力下的正常血液,6小时的急性肾下主动脉闭塞将导致严重的再灌注损伤(缺血后综合征)。相比之下,通过控制性肢体再灌注对缺血骨骼肌进行初始治疗可减少代谢、功能和生化改变。