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在白细胞滤除红细胞储存过程中,葡萄糖-6-磷酸脱氢酶活性降低。

Glucose-6-phosphate dehydrogenase activity decreases during storage of leukoreduced red blood cells.

作者信息

Peters Anna L, van Bruggen Robin, de Korte Dirk, Van Noorden Cornelis J F, Vlaar Alexander P J

机构信息

Laboratory of Experimental Intensive Care and Anesthesia/Intensive Care, Academic Medical Centre.

Department of Blood Cell Research, Sanquin Blood Bank, Amsterdam, the Netherlands.

出版信息

Transfusion. 2016 Feb;56(2):427-32. doi: 10.1111/trf.13378. Epub 2015 Oct 12.

Abstract

BACKGROUND

During storage, the activity of the red blood cell (RBC) antioxidant system decreases. Glucose-6-phosphate dehydrogenase (G6PD) is essential for protection against oxidative stress by producing NADPH. G6PD function of RBC transfusion products is reported to remain stable during storage, but activity was measured in hemolysates and not in individual RBCs. We hypothesized that analysis of G6PD activity in individual RBC identifies storage-dependent changes in G6PD function.

STUDY DESIGN AND METHODS

Seven units of stored leukoreduced RBCs, stored in saline-adenine-glucose-mannitol, were sampled every week up to 6 weeks of storage. G6PD activity was determined with the cytofluorometric method and expressed as mean fluorescent intensity (MFI) per RBC.

RESULTS

During storage, G6PD activity decreased significantly. Mean MFI after 3 days of storage was 27.8 ± 8.8 and gradually decreased significantly to 18.0 ± 8.3 after 42 days.

CONCLUSION

G6PD activity decreases during storage of leukoreduced RBCs. Our results may form a new target to improve storage conditions of RBCs and subsequently improve the quality of transfusion products.

摘要

背景

在储存过程中,红细胞(RBC)抗氧化系统的活性会降低。葡萄糖-6-磷酸脱氢酶(G6PD)通过产生还原型辅酶II(NADPH)对抵御氧化应激至关重要。据报道,红细胞输血产品中的G6PD功能在储存期间保持稳定,但活性是在溶血产物中测量的,而非单个红细胞。我们推测,对单个红细胞中G6PD活性的分析可识别出G6PD功能中与储存相关的变化。

研究设计与方法

七单位储存于生理盐水-腺嘌呤-葡萄糖-甘露醇中的白细胞滤除红细胞,在储存长达6周的时间里每周进行采样。采用细胞荧光测定法测定G6PD活性,并表示为每个红细胞的平均荧光强度(MFI)。

结果

在储存期间,G6PD活性显著降低。储存3天后的平均MFI为27.8±8.8,在42天后逐渐显著降低至18.0±8.3。

结论

在白细胞滤除红细胞的储存过程中,G6PD活性降低。我们的结果可能形成一个新的靶点,以改善红细胞的储存条件,进而提高输血产品的质量。

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