Salvianolic acid B alleviates red blood cell storage lesion with GPX4 preservation and reduced lipid peroxidation.

Chuan'ai Chen, Dekun Wang, Yang Yu, Pengpeng An, Yumiao Yang, Haolong Li
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Abstract

Background: Red blood cell (RBC) storage lesion is a cascade of biochemical and physical alterations that impair transfusion efficacy and safety. This study explored the role and underlying mechanism of salvianolic acid B (Sal B) against RBC storage lesion, with a specific focus on a ferroptosis-like process.

Materials and methods: RBC from healthy volunteers were stored in MAP additive solution for 35 days, and samples were analyzed at weekly intervals. Ferroptosis was determined by the levels of cytosolic reactive oxygen species (ROS), antioxidant enzymes superoxide dismutase and glutathione peroxidase, 4-hydroxy-2-nonenal (4-HNE), malondialdehyde (MDA), and glutathione peroxidase 4 (GPX4). Storage lesion was evaluated by erythrocyte morphology, hemolysis rate, microvesicle formation, phosphatidylserine exposure, lactate dehydrogenase release, osmotic fragility, and Band 3. Ferrostatin-1 was used to verify the involvement of ferroptosis.

Results: The results demonstrated a time-dependent escalation of both storage lesion and ferroptosis, evidenced by biochemical changes such as increased hemolysis, phosphatidylserine exposure, ROS accumulation, 4-HNE and MDA, as well as a reduction in antioxidant capacity and protein level of GPX4. Ferrostatin-1 treatment effectively mitigated pathological changes, suggesting that ferroptosis-associated pathways may contribute to storage lesion. Notably, Sal B supplementation correlated with reduced ferroptosis markers and mitigation of storage lesion, as evidenced by preserved GPX4 levels and reduced lipid peroxidation.

Discussion: This study demonstrates that a ferroptosis-like process of lipid peroxidation contributes to RBC storage lesion, with GPX4 regulating erythrocyte stability. Sal B alleviates storage lesion in parallel with preservation of GPX4 and reduced lipid peroxidation, providing a potential strategy to improve the quality of stored blood.

丹酚酸B通过GPX4保存和减少脂质过氧化减轻红细胞储存损伤。
背景:红细胞(RBC)储存损伤是一系列生化和物理改变,影响输血的有效性和安全性。本研究探讨了丹酚酸B (salvianolic acid B, Sal B)对红细胞储存损伤的作用和潜在机制,并特别关注了嗜铁样过程。材料与方法:将健康志愿者的红细胞在MAP添加液中保存35天,每隔一周对样本进行分析。通过胞质活性氧(ROS)、抗氧化酶超氧化物歧化酶和谷胱甘肽过氧化物酶、4-羟基-2-壬烯醛(4- hne)、丙二醛(MDA)和谷胱甘肽过氧化物酶4 (GPX4)的水平检测铁凋亡。通过红细胞形态、溶血率、微泡形成、磷脂酰丝氨酸暴露、乳酸脱氢酶释放、渗透脆性和能带3来评估储存损伤。使用铁抑素-1来验证铁下垂的累及。结果:结果显示贮藏损伤和铁下垂均呈时间依赖性升级,表现为溶血、磷脂酰丝氨酸暴露、ROS积累、4-HNE和MDA增加等生化变化,以及GPX4抗氧化能力和蛋白水平降低。他汀-1治疗有效地减轻了病理变化,提示铁中毒相关途径可能有助于储存病变。值得注意的是,补充Sal B与降低铁下垂标志物和减轻储存损伤相关,这一点可以通过保持GPX4水平和减少脂质过氧化得到证明。讨论:本研究表明,类似铁中毒的脂质过氧化过程导致红细胞储存损伤,GPX4调节红细胞稳定性。Sal B在保护GPX4和减少脂质过氧化的同时减轻了储存损伤,为改善储存血液的质量提供了一种潜在的策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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