Nagababu Enika, Scott Andrew V, Johnson Daniel J, Dwyer Ian M, Lipsitz Joshua A, Barodka Viachaslau M, Berkowitz Dan E, Frank Steven M
Department of Anesthesiology/Critical Care Medicine, the Johns Hopkins Medical Institutions, Baltimore, Maryland.
Transfusion. 2016 May;56(5):1101-11. doi: 10.1111/trf.13458. Epub 2016 Jan 6.
The loss of structural and functional integrity of red blood cells (RBCs) during storage, collectively referred to as "storage lesion," has been implicated in reduced oxygen delivery after transfusion. RBCs are highly susceptible to oxidative damage from generation of reactive oxygen species by autoxidation of hemoglobin. Therefore, we examined whether increased oxidative stress (OS) in stored RBCs is associated with impaired cell membrane deformability before or after transfusion.
Thirty-four patients undergoing multilevel spine fusion surgery were enrolled. OS in RBCs was assessed by the presence of fluorescent heme degradation products and methemoglobin, which were measured with fluorimetric and spectrophotometric methods, respectively. Deformability and aggregation were determined by ektacytometry in stored RBCs, autologous salvaged RBCs, and posttransfusion blood samples.
OS in stored RBCs was significantly increased with longer storage (R = 0.54, p = 0.032) and significantly higher than that in fresh RBCs (9.1 ± 1.3 fluorescent arbitrary units vs. 7.7 ± 0.9 fluorescent arbitrary units, p < 0.001). Deformability decreased (R = -0.60, p = 0.009) with increasing storage duration. OS was elevated (p < 0.05) and deformability was decreased (p < 0.05) in postoperative blood from patients who had undergone moderate (≥4 RBC units) but not minimal or no transfusion. Neither the decrease in deformability of RBCs nor the aggregation changes were correlated with OS.
Although stored RBCs show signs of increased OS and loss of cell membrane deformability, these changes were not directly correlated and were only evident after moderate but not lower dose transfusion in postoperative surgical patients. These findings suggest that factors other than OS may contribute to impaired rheology with stored RBCs in the clinical setting.
红细胞(RBC)在储存期间结构和功能完整性的丧失,统称为“储存损伤”,与输血后氧输送减少有关。红细胞极易受到血红蛋白自氧化产生的活性氧物种引起的氧化损伤。因此,我们研究了储存红细胞中氧化应激(OS)增加是否与输血前后细胞膜变形性受损有关。
招募了34例接受多级脊柱融合手术的患者。通过荧光血红素降解产物和高铁血红蛋白的存在评估红细胞中的氧化应激,分别用荧光法和分光光度法进行测量。通过激光衍射法测定储存红细胞、自体回收红细胞和输血后血样中的变形性和聚集性。
储存红细胞中的氧化应激随着储存时间的延长而显著增加(R = 0.54,p = 0.032),且显著高于新鲜红细胞(9.1±1.3荧光任意单位对7.7±0.9荧光任意单位,p < 0.001)。随着储存时间的增加,变形性降低(R = -0.60,p = 0.009)。接受中度(≥4个红细胞单位)输血但非少量或未输血的患者术后血液中氧化应激升高(p < 0.05),变形性降低(p < 0.05)。红细胞变形性的降低和聚集性的变化均与氧化应激无关。
尽管储存红细胞显示出氧化应激增加和细胞膜变形性丧失的迹象,但这些变化并无直接关联,且仅在术后手术患者接受中度而非较低剂量输血后才明显。这些发现表明,在临床环境中,除氧化应激外的其他因素可能导致储存红细胞的流变学受损。