Department of Biotechnology, School of Sciences, Block I, JAIN (Deemed-to-be University), #18/3, 9th Main, 3rd Block, Jayanagar, Bengaluru, 560011, India.
Kempegowda Institute of Medical Sciences (KIMS) Hospital, Department of Emergency Medicine, Krishna Rajendra Road, Parvathipuram, Vishweshwarapura, Basavanagudi, Bengaluru, 560004, India.
Transfus Apher Sci. 2020 Dec;59(6):102905. doi: 10.1016/j.transci.2020.102905. Epub 2020 Aug 3.
Blood and its components are stored to meet the demands of blood transfusion. Erythrocytes undergo progressive modifications during storage known as storage lesions. Storage solutions were developed to improve shelf life and extend red cell viability. Therefore, the objective of this study is to analyze the effects of AS-7 on young and old erythrocytes during storage. Blood was collected from the blood bank at Kempegowda Institute of Medical Sciences (KIMS) hospital, Bengaluru. Erythrocytes were isolated from whole blood and separated based on its age using Percoll density gradient. The young and old erythrocytes were stored in AS-7 for 35 days and every 5th day, oxidative stress markers - Hemoglobin (Hb), Oxidative Hemolysis, Mechanical Fragility, Sialic Acid, Superoxides, Glucose, Lactate Dehydrogenase (LDH), Glutathione, antioxidant capacity (TAC), Plasma Membrane Redox System (PMRS), antioxidant enzymes, lipid peroxidation, and protein oxidation products were assessed. Hb, glucose, TAC and superoxide dismutase reduced, while oxidative hemolysis, mechanical fragility, protein oxidation, and lipid peroxidation products increased in young and old cells over storage. LDH, PMRS, catalase, advanced oxidation protein products, and conjugate dienes were significant in old cells from day 5 itself, whereas in young cells towards the end of storage (from day 25). Oxidative insult was higher in old cells compared to young cells. AS-7 was beneficial to young erythrocytes during storage and thus laying the foundation for the possibilities of utilizing young cells as models for storage studies.
血液及其成分被储存以满足输血需求。红细胞在储存过程中会发生渐进性改变,称为储存损伤。储存液的开发旨在延长保质期并延长红细胞的存活时间。因此,本研究的目的是分析 AS-7 在储存过程中对年轻和衰老红细胞的影响。从班加罗尔的 Kempegowda 医学科学研究所 (KIMS) 医院的血库采集血液。从全血中分离出血细胞,并使用 Percoll 密度梯度根据其年龄进行分离。将年轻和衰老的红细胞储存在 AS-7 中 35 天,每隔 5 天测量一次氧化应激标志物 - 血红蛋白 (Hb)、氧化溶血、机械脆性、唾液酸、超氧化物、葡萄糖、乳酸脱氢酶 (LDH)、谷胱甘肽、抗氧化能力 (TAC)、血浆膜氧化还原系统 (PMRS)、抗氧化酶、脂质过氧化和蛋白质氧化产物。Hb、葡萄糖、TAC 和超氧化物歧化酶减少,而年轻和衰老细胞的氧化溶血、机械脆性、蛋白质氧化和脂质过氧化产物在储存过程中增加。LDH、PMRS、过氧化氢酶、高级氧化蛋白产物和共轭二烯在第 5 天的衰老细胞中显著,而在年轻细胞中则在储存结束时(第 25 天)。与年轻细胞相比,衰老细胞的氧化损伤更高。AS-7 在储存过程中对年轻红细胞有益,从而为利用年轻细胞作为储存研究模型奠定了基础。