Dipartimento di Scienze Chimiche, Laboratorio di Biochimica, Università di Catania, Italy.
Blood Transfus. 2007 Jan;5(1):24-32. doi: 10.2450/2007.0019-06.
Therapeutic storage of platelet concentrate is a challenging problem for Transfusion Medicine, so that many studies have been carried out with the aim of improving the duration of storage of platelet concentrates. Little attention, however, has been given to the most appropriate biochemical methods for evaluating the quality of the stored platelet concentrates.
[corrected] Platelet concentrates (n=10) were saved under gentle stirring at 22 masculineC for a total period of 8 days. Glucose 0.5% (w/v) was added either at the beginning of storage (time 0) or on the fifth day of storage. One millilitre of each concentrate was withdrawn at time 0 and after 5, 6, 7 and 8 days of storage for microbiological culture, evaluation of pH, lactate dehydrogenase (LDH), mean platelet volume, platelet haematocrit and analysis of metabolites of energy pathways (high energy phosphate derivatives, nucleosides, oxypurines and antioxidants) by high performance liquid chromatography.
The addition of glucose 0.5% on day 5 did not produce significant differences in metabolites of energy pathways with respect to control platelet concentrates, whereas when the glucose was added at the beginning of storage (time 0) there was a recovery of ATP, GTP and a decrease of energetic catabolism, demonstrating a beneficial effect on energy metabolism. The changes in LDH values did not parallel those of the metabolites: indeed, only on day 7 of storage did the platelet concentrates treated with glucose on day 5 have significantly lower levels of this enzyme than those found in the other concentrates. The improvements produced by addition of glucose at time 0 were confirmed by morphological analyses (mean platelet volume, platelet haematocrit), and the pH.
The metabolic profile of glucose-enriched plasma concentrates on the fifth day of storage, and the different time course of increased LDH concentration, could represent valid parameters to interpret platelet vitality in the successive days of storage. These preliminary data also indicate that glucose might be a good additive for a new storage formulation.
治疗性储存血小板浓缩物是输血医学面临的一个挑战,因此许多研究旨在提高血小板浓缩物的储存时间。然而,很少有人关注最适合评估储存血小板浓缩物质量的生化方法。
将血小板浓缩物(n=10)在 22°C 下温和搅拌保存,总保存期为 8 天。在储存开始时(时间 0)或储存第 5 天添加 0.5%(w/v)葡萄糖。在时间 0 以及储存第 5、6、7 和 8 天,从每个浓缩物中抽取 1 毫升进行微生物培养、pH 值、乳酸脱氢酶(LDH)、平均血小板体积、血小板比容和能量代谢途径代谢产物(高能磷酸衍生物、核苷、氧化嘌呤和抗氧化剂)分析。
与对照血小板浓缩物相比,在第 5 天添加 0.5%葡萄糖并未在能量代谢产物方面产生显著差异,而在储存开始时(时间 0)添加葡萄糖时,ATP、GTP 恢复,能量代谢消耗减少,对能量代谢有有益影响。LDH 值的变化与代谢产物的变化不一致:事实上,只有在第 7 天储存时,第 5 天添加葡萄糖的血小板浓缩物的酶水平明显低于其他浓缩物。在时间 0 添加葡萄糖产生的改善通过形态分析(平均血小板体积、血小板比容)和 pH 值得到证实。
在第 5 天储存的富含葡萄糖的血浆浓缩物的代谢谱以及 LDH 浓度增加的不同时间过程,可能代表解释储存后连续几天血小板活力的有效参数。这些初步数据还表明,葡萄糖可能是新储存配方的良好添加剂。