Edenbrandt C M, Murphy S
Cardeza Foundation for Hematologic Research, Jefferson Medical College, Thomas Jefferson University, Philadelphia, PA 19107.
Blood. 1990 Nov 1;76(9):1884-92.
Adenine and guanine nucleotide metabolism of platelet concentrates (PCs) was studied during storage for transfusion at 22 +/- 2 degrees C over a 7-day period using high-pressure liquid chromatography. There was a steady decrease in platelet adenosine triphosphate (ATP) and adenosine diphosphate (ADP), which was balanced quantitatively by an increase in plasma hypoxanthine. As expected, ammonia accumulated along with hypoxanthine but at a far greater rate. A fall in platelet guanosine triphosphate (GTP) and guanosine diphosphate (GDP) paralleled the fall in ATP + ADP. When adenine was present in the primary anticoagulant, it was carried over into the PC and metabolized. ATP, GTP, total adenine nucleotides, and total guanine nucleotides declined more slowly in the presence of adenine than in its absence. With adenine, the increase in hypoxanthine concentration was more rapid and quantitatively balanced the decrease in adenine and platelet ATP + ADP. Plasma xanthine rose during storage but at a rate that exceeded the decline in GTP + GDP. When platelet ATP + ADP was labeled with 14C-adenine at the initiation of storage, half of the radioactivity was transferred to hypoxanthine (45%) and GTP + GDP + xanthine (5%) by the time storage was completed. The isotopic data were consistent with the presence of a radioactive (metabolic) and a nonradioactive (storage) pool of ATP + ADP at the initiation of storage with each pool contributing approximately equally to the decline in ATP + ADP during storage. The results suggested a continuing synthesis of GTP + GDP from ATP + ADP, explaining the slower rate of fall of GTP + GDP relative to the rate of rise of plasma xanthine. Throughout storage, platelets were able to incorporate 14C-hypoxanthine into both adenine and guanine nucleotides but at a rate that was only one fourth the rate of hypoxanthine accumulation. All of these data should be helpful in improving the function and viability of PC as currently stored for 5 days, in devising methods for storage beyond 5 days, and in the development of synthetic media for PC storage.
使用高压液相色谱法,在22±2℃下储存7天的过程中,对用于输血的血小板浓缩物(PCs)的腺嘌呤和鸟嘌呤核苷酸代谢进行了研究。血小板三磷酸腺苷(ATP)和二磷酸腺苷(ADP)稳步下降,血浆次黄嘌呤增加在数量上与之平衡。正如预期的那样,氨与次黄嘌呤一起积累,但速度要快得多。血小板三磷酸鸟苷(GTP)和二磷酸鸟苷(GDP)的下降与ATP + ADP的下降平行。当腺嘌呤存在于初始抗凝剂中时,它会带入PC并被代谢。在有腺嘌呤存在的情况下,ATP、GTP、总腺嘌呤核苷酸和总鸟嘌呤核苷酸的下降比没有腺嘌呤时更慢。有腺嘌呤时,次黄嘌呤浓度的增加更快,并且在数量上平衡了腺嘌呤和血小板ATP + ADP的减少。储存期间血浆黄嘌呤升高,但速度超过了GTP + GDP的下降。当在储存开始时用14C - 腺嘌呤标记血小板ATP + ADP时,到储存结束时,一半的放射性转移到了次黄嘌呤(45%)和GTP + GDP + 黄嘌呤(5%)。同位素数据与储存开始时存在放射性(代谢)和非放射性(储存)的ATP + ADP池一致,每个池对储存期间ATP + ADP的下降贡献大致相等。结果表明从ATP + ADP持续合成GTP + GDP,这解释了GTP + GDP相对于血浆黄嘌呤上升速度下降较慢的原因。在整个储存过程中,血小板能够将14C - 次黄嘌呤掺入腺嘌呤和鸟嘌呤核苷酸中,但速度仅为次黄嘌呤积累速度的四分之一。所有这些数据对于改善目前储存5天的PC的功能和活力、设计超过5天的储存方法以及开发用于PC储存的合成培养基应该是有帮助的。