Nakao M, Nakao T, Nakayama T, Nagai F, Dogen M
Acta Biol Med Ger. 1981;40(7-8):1003-8.
Among 15 enzymes PFK decreased most during preservation at 4 degrees C for 6-8 weeks, and this was prevented by the addition of adenine and inosine, but not by adenine or inosine only. PFK inactivation in hemolysate was also prevented by ATP. In order to maintain low fragility, isotonic sucrose solution was newly devised. Maltose and lactose followed and mannitol was also effective. The decrease in fragility accompanied the decrease in the cell volume and the increase of Na+, K+, H+ and Cl- in the medium. However, the filtrability of red cells was sometimes decreased in case of extremely lowered fragility. Therefore, appropriate ratios of isoosmotic sucrose (hardly permeable) and NaCl (relatively rapidly permeable) solutions must be selected for preservation of blood. Various properties in vitro of rabbit cells were well maintained and their posttransfusion viability was also prolonged when using this medium. Elimination of hypoxanthine could be achieved by hydron coated charcoal prior to transfusion.
在15种酶中,磷酸果糖激酶(PFK)在4℃保存6 - 8周期间下降最为显著,添加腺嘌呤和肌苷可防止这种情况发生,但仅添加腺嘌呤或肌苷则无效。ATP也可防止溶血产物中PFK的失活。为了维持低脆性,新设计了等渗蔗糖溶液。麦芽糖和乳糖次之,甘露醇也有效。脆性的降低伴随着细胞体积的减小以及培养基中Na +、K +、H +和Cl - 的增加。然而,在脆性极低的情况下,红细胞的过滤性有时会降低。因此,为了保存血液,必须选择等渗蔗糖(几乎不可渗透)和NaCl(相对快速渗透)溶液的适当比例。使用这种培养基时,兔细胞的各种体外特性得到了良好维持,其输血后的存活率也得以延长。输血前通过氢包裹活性炭可实现次黄嘌呤的清除。