Markov A K, Terry J, White T Z, Didlake R H, Hellems H K
Surgery. 1987 Sep;102(3):515-27.
Previous reports from this laboratory described animal experiments in which intravenous administration of fructose 1-6 diphosphate (FDP) at the onset of hypovolemia, toxemia, and trauma effected improvement in hemodynamic and metabolic parameters, attenuation of tissue damage, and a significant increase in survival. The obvious question remained: Would this agent be as effective if administered after the onset of the shock syndrome? Thus 72 anesthetized dogs were subjected to normotensive hemorrhagic shock and were subsequently treated with FDP at 30 minutes, 1 hour, 90 minutes, and 2 hours after exsanguination. Analysis of the results (as compared with vehicle-treated controls) revealed evidence of improved cardiac output and arterial pressure (p less than 0.02), conservation of effective circulatory volume, better oxygen utilization, and a significant increase in survival (p less than 0.0001). These results, in conjunction with earlier experimental and recent clinical data, indicate that the therapeutic effect of FDP in ischemic and hypoperfusion states is in part metabolically mediated by the augmentation of carbohydrate utilization. Prevention of tissue injury is in part due to the inhibition of generation of oxygen-derived free radicals by neutrophils.
该实验室之前的报告描述了动物实验,即在低血容量、毒血症和创伤发生时静脉注射1,6-二磷酸果糖(FDP)可改善血流动力学和代谢参数,减轻组织损伤,并显著提高存活率。一个明显的问题仍然存在:如果在休克综合征发作后给药,这种药物是否同样有效?因此,72只麻醉犬接受了正常血压性出血性休克实验,随后在放血后30分钟、1小时、90分钟和2小时用FDP进行治疗。结果分析(与用赋形剂处理的对照组相比)显示,心输出量和动脉压有所改善(p<0.02),有效循环血量得以维持,氧利用情况更好,存活率显著提高(p<0.0001)。这些结果,连同早期的实验和近期的临床数据表明,FDP在缺血和低灌注状态下的治疗作用部分是通过增加碳水化合物利用在代谢上介导的。预防组织损伤部分是由于抑制了中性粒细胞产生氧衍生的自由基。