Jesch F H, Peters W, Hobbhahn J, Schoenberg M, Messmer K
Crit Care Med. 1982 Apr;10(4):270-4. doi: 10.1097/00003246-198204000-00007.
The hemodynamic effectiveness and the oxygen characteristics of stroma-free hemoglobin (SFH) solutions were studied in 11 dogs. the animals were bled two-thirds of the estimated blood volume or until cardiac arrest. The shed blood was immediately replaced by equivalent amounts of either SFH or polyhemoglobin (SFH-PLP). Sixty min later, Ringer's lactate was given iv for 180 min to maintain right atrial pressure at the initial value. In a second set of experiments, the intravascular persistence of SFH-PLP was investigated in 5 dogs by withdrawal of blood (7 ml/kg bw) and immediate replacement with 131I-labeled SFH-PLP. Hemodynamic disorders after severe blood loss could be reversed by infusion of hemoglobin solutions. Due to the short intravascular persistence, cardiac output did not increase as one would expect from the degree of hemodilution. Pyridoxalation of the hemoglobin molecule reduced oxygen affinity and improved oxygen unloading at the tissue level. The short intravascular half-time of this compound could be overcome by crosslinking of the pyridoxalated hemoglobin molecules. Further studies must prove whether this polyhemoglobin can be used as a long-term oxygen-carrying blood substitute.
在11只狗身上研究了无基质血红蛋白(SFH)溶液的血流动力学效应和氧特性。动物被放血至估计血容量的三分之二或直至心脏骤停。流出的血液立即用等量的SFH或多聚血红蛋白(SFH-PLP)替代。60分钟后,静脉输注乳酸林格液180分钟,以将右心房压力维持在初始值。在第二组实验中,通过抽取血液(7 ml/kg体重)并用131I标记的SFH-PLP立即替代,研究了5只狗体内SFH-PLP的血管内持久性。严重失血后的血流动力学紊乱可通过输注血红蛋白溶液得到逆转。由于血管内持久性短,心输出量并未如预期的那样因血液稀释程度而增加。血红蛋白分子的吡哆醛化降低了氧亲和力并改善了组织水平的氧卸载。这种化合物的血管内半衰期短可通过吡哆醛化血红蛋白分子的交联来克服。进一步的研究必须证明这种多聚血红蛋白是否可作为长期携氧血液替代品使用。