Pristoupil T I, Vrána M, Havlícková J, Kramlová M
Institute of Hematology and Blood Transfusion, Prague, Czechoslovakia.
Int J Artif Organs. 1989 Oct;12(10):668-72.
The addition of stroma-free hemoglobin solution to a standard St. Thomas Hospital cardioplegic solution significantly protected the heart from ischemic damage compared to the effect of the same solution without added hemoglobin. An experimental model of rat heart cardioplegia and transplantation comprising heart arrest for three hours at 20 degrees C was used. The number of hearts performing strong contractions after cardioplegia with iso-oncotic oxyhemoglobin prior to transplantation was close to the results with histidine-buffered cardioplegic solution according to Bretschneider. Comparative biochemical model experiments in vitro confirmed that the positive effect of oxyhemoglobin was due predominantly to its buffering capacity. The role of oxygen transport to tissues by hemoglobin was limited only to the first minutes of cardioplegia since neither recirculation nor reoxygenation took place in the present experimental setting.
与未添加血红蛋白的相同溶液相比,在标准的圣托马斯医院心脏停搏液中添加无基质血红蛋白溶液可显著保护心脏免受缺血性损伤。采用大鼠心脏停搏和移植的实验模型,包括在20摄氏度下心脏停搏3小时。根据Bretschneider的研究,移植前用等渗氧合血红蛋白进行心脏停搏后表现出强烈收缩的心脏数量与组氨酸缓冲心脏停搏液的结果相近。体外比较生化模型实验证实,氧合血红蛋白的积极作用主要归因于其缓冲能力。由于在本实验环境中既没有再循环也没有再氧合,血红蛋白向组织输送氧气的作用仅局限于心脏停搏的最初几分钟。