• 中国科学论文统计源期刊
  • 中国科技核心期刊
  • 美国化学文摘(CA)来源期刊
  • 日本科学技术振兴机构数据库(JST)

临床输血与检验 ›› 2025, Vol. 27 ›› Issue (6): 775-782.DOI: 10.3969/j.issn.1671-2587.2025.06.005

• 基础研究 • 上一篇    下一篇

氢气抑制单采血小板活化和凋亡的作用研究*

李津杞1, 秦爱华1, 任瑜菲2, 唐河山1, 陈翠敏2, 钱宝华1, 臧艳1   

  1. 1中国人民解放军海军军医大学第一附属医院输血科,上海 200433;
    2中国人民解放军海军军医大学第一附属医院临床研究中心,上海 200433
  • 收稿日期:2025-03-25 出版日期:2025-12-20 发布日期:2025-12-24
  • 通讯作者: 臧艳,主要从事输血科质量控制方面研究,E-mail:13817145306@163.com。共同通信作者:钱宝华,主要从事合理输血方面研究,E-mail:qianbh1963@163.com。
  • 作者简介:李津杞,主要从事血液保存和质量控制方面研究,E-mail:ljq_421@163.com。并列第一作者:秦爱华,主要从事输血治疗方面研究,E-mail:qinaihua729@126.com。
  • 基金资助:
    *本课题受海军军医大学第一附属医院“234学科攀峰计划”(No.2020YXK036)资助

Inhibitory Effects of Hydrogen on Activation and Apoptosis in Stored Apheresis Platelets

LI Jinqi1, QIN Aihua1, REN Yufei2, TANG Heshan1, CHEN Cuimin2, QIAN Baohua1, ZANG Yan1   

  1. 1Department of Transfusion Medicine, First Affiliated Hospital of Naval Medical University, Shanghai 200433;
    2Clinical Research Center of the First Affiliated Hospital of Naval Medical University, Shanghai 200433
  • Received:2025-03-25 Online:2025-12-20 Published:2025-12-24

摘要: 目的 探索氢气(hydrogen, H2)抑制单采血小板活化和凋亡的作用研究。方法 10份单采血小板,每份平均装入16小袋中,随机分为H2组和对照组,H2组加入H2至饱和,并每天补充H2。(22±2)℃振荡保存8天,每天检测血小板计数,流式检测CD62P、PAC-1及凋亡的百分比,Western blotting检测Caspase-3、Caspase-9、Bax、Bcl-2蛋白的表达水平。结果 血小板计数在保存期间(1~8天)的差异均无统计学意义。但流式实验的凋亡指标从第5天开始,H2组的比例比对照组低(20.29±4.32 vs 33.06±8.01,P<0.001);活化指标CD62P从第6天开始,H2组比对照组低(24.94±5.53 vs 47.14 ±10.41,P<0.001),PAC-1从第6天开始,H2组比对照组低(14.89±5.98 vs 19.41±5.17,P<0.05),差异有统计学意义。Western blotting结果显示从第6天开始,H2组cleaved Caspase-9和cleaved Caspase-3含量表达比对照组低(P<0.001),第7天开始,H2组Bax含量表达比对照组低(P<0.001),Bcl-2比对照组高(P<0.05),Bax/Bcl-2的比值比对照组低,差异有统计学意义(P<0.001)。结论 H2可以抑制单采血小板活化和凋亡,一定程度上改善保存质量。

关键词: 氢气, 血小板保存损伤, 活化, 凋亡

Abstract: Objective To explore the effect and mechanism of hydrogen (H2) on apheresis platelets activation and apoptosis. Methods 10 apheresis platelets were divided equally into 16 small bags and randomly divided into an H2 group and a control group. The H2 group was added with hydrogen to saturation and supplemented with hydrogen daily. All samples were stored under agitation at (22±2) ℃ for 8 days, the platelet count was tested, and the CD62P, PAC-1, apoptosis were detected by flow cytometry daily. The Caspase-3, Caspase-9, Bax, and Bcl-2 proteins were detected by Western blotting. Results There was no significant difference in platelet count during the preservation period (1~8 d). From the fifth day, the apoptosis rate in H2 group was significantly lower than that in the control group (20.29±4.32 vs 33.06±8.01, P<0.001). From the sixth day, the expression of CD62P in H2 group was lower than that in the control group (24.94±5.53 vs 47.14±10.41, P<0.001), and the expression of PAC-1 in H2 group was lower than that in the control group (14.89±5.98 vs 19.41±5.17, P<0.05). Western blotting results showed that from the sixth day, the expression of cleaved Caspase-9 and cleaved Caspase-3 in the H2 group was lower than that in the control group (P<0.001). From the seventh day, the expression of Bax in the H2 group was lower than that in the control group (P<0.001), while Bcl-2 was higher than that in the control group (P<0.05), the ratio of Bax/Bcl-2 was lower than that of the control group. Conclusion Hydrogen can reduce platelet activation and apoptosis, improve the quality of apheresis platelet storage.

Key words: Hydrogen, Platelet storage lesion, Activation, Apoptosis

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