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首页|期刊导航|中国临床医学影像杂志|T2* mapping MR成像评价脊髓缺血再灌注后铁死亡的机制研究

T2* mapping MR成像评价脊髓缺血再灌注后铁死亡的机制研究OACSTPCD

The mechanism of ferroptosis after spinal cord ischemia-reperfusion evaluated by T2* mapping MR

中文摘要英文摘要

目的:通过 7.0T T2* mapping MR成像技术检测脊髓缺血再灌注(Spinal cord ischemia-reperfusion,SCIR)损伤后脊髓前角铁沉积变化,并分析其与铁死亡蛋白变化的关系,以此反映SCIR后铁死亡的作用机制.方法:选取 48 只Wistar大鼠(雄性,280~300 g),随机分为假手术组(n=8)和SCIR实验组(n=40).实验组按缺血再灌注后不同恢复时间分为 6h组(n=8),12 h组(n=8),24 h组(n=8),48 h组(n=8)和 72h组(n=8).建模完成后进行 7.0T MR扫描.扫描后进行脊髓组织溶质载体家族 11成员 2(Solute carrier family 11 member 2,SLC11A2)、铁蛋白重链 1(Ferritin heavy chain 1,FTH1)、谷胱甘肽过氧化物酶 4(Glutathione peroxidase 4,GPX4)的免疫组化染色.采用方差分析、Tukey检验比较各组T2*值和蛋白质表达水平的差异.结果:SCIR后 6h,脊髓前角T2*值显著降低(P<0.001,Tukey检验),至 24h达到最低(P<0.001,Tukey检验),48 h组回升(P<0.001).SCIR损伤后 6 h,SLC11A2 表达具有轻度增加趋势,FTH1 表达显著降低(P=0.007,Tukey检验),SCIR损伤后 24 h,SLC11A2、FTH1、GPX4 表达均显著降低(P=0.031,P=0.009,P=0.004,Tukey检验).结论:SCIR损伤后脊髓前角T2*值、SLC11A2、FTH1、GPX4 均出现一过性降低过程,且T2*变化与GPX4 蛋白变化一致,提示T2* mapping可通过检测脊髓铁沉积的变化进一步反映铁死亡的作用机制.

Objective:To examine the changes of iron deposition in the spinal cord by 7.0T T2* mapping MR imaging af-ter spinal cord ischemia-reperfusion(SCIR)and analyze the relationship between T2* and protein of ferroptosis,to reflect the mechanism of ferroptosis after SCIR.Methods:Forty-eight Wistar rats(male,280~300 g)were selected and randomly divided into sham group(n=8)and SCIR group(n=40).The SCIR group was divided into 6 h(n=8),12 h(n=8),24 h(n=8),48 h(n=8)and 72 h(n=8)subgroups.A 7.0T MR scan was performed after the modeling was completed.After scanning,immunohistochemical staining of family 11 member 2(SLC11A2),ferritin heavy chain 1(FTH1),glutathione peroxidase 4(GPX4)were performed.Analysis of variance and Tukey test were used to compare the differences in T2* values and protein expression levels in each group.Results:At 6 h after SCIR,the T2* value of the anterior spinal horn decreased significantly(P<0.001,Tukey test),reaching the lowest at 24 h(P<0.001,Tukey test),and the 48 h subgroup recovered(P<0.001).At 6 h after the SCIR injury,SLC11A2 expression showed a slight increase trend,while FTH1 expression was significantly reduced(P=0.007,Tukey test).At 24 h after the SCIR injury,the expression of SLC11A2,FTH1,and GPX4 were significantly decreased(P=0.031,P=0.009,P= 0.004,Tukey test).Conclusion:After SCIR injury,the T2* value,SLC11A2,FTH1,and GPX4 all show a transient decrease,and the T2* change is consistent with the GPX4 protein change,suggesting that T2* mapping can further reflect the mecha-nism of ferroptosis by detecting the changes in spinal iron deposition.

李可心;郑阳;袁正伟;王晓明

中国医科大学附属盛京医院放射科,辽宁 沈阳 110004中国医科大学附属盛京医院 国家卫健委小儿先天畸形重点实验室,辽宁 沈阳 110004

临床医学

脊髓缺血磁共振成像

Spinal Cord IschemiaIronMagnetic Resonance Imaging

《中国临床医学影像杂志》 2024 (001)

神经管畸形发生的关键基因筛选、验证及交互调控新机制研究

7-10 / 4

国家重点研发计划(2021YFC2701104,2021YFC2701003);国家自然科学基金项目(No:82171649);中国博士后科学基金(2023M743906).

10.12117/jccmi.2024.01.002

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