首页|姜黄素通过抑制TXNIP/TRX-1/GPX4通路介导的铁死亡减轻脓毒症小鼠肺损伤

姜黄素通过抑制TXNIP/TRX-1/GPX4通路介导的铁死亡减轻脓毒症小鼠肺损伤

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目的 探究姜黄素(Cur)是否通过调控TXNIP/TRX-1/GPX4通路抑制铁死亡减轻脓毒症肺损伤。方法 雄性C57BL/6小鼠随机分为Sham组、脓毒症(盲肠结扎穿孔术,CLP)组、CLP+各浓度Cur(50、100和200 mg/kg)组、CLP+Cur(200 mg/kg)+TRX-1抑制剂PX-12(25 mg/kg)组,10只/组,检测各组小鼠肺组织炎症因子及铁死亡关键因子MDA、MPO、GSH水平。Beas-2B细胞分为Con组、脂多糖组(LPS,1 μg/mL)、LPS+各浓度Cur(2。5、5、10 μmol/L)及LPS+Cur(10 μmol/L)+PX-12(5 μmol/L)组,检测MDA和Fe2+水平,DHE染色评估ROS变化。Western blotting检测肺组织和Beas-2B细胞TXNIP、TRX-1、GPX4和X-CT蛋白表达水平。结果 与Sham组相比,CLP组小鼠肺损伤严重,IL-6、IL-1β、TNF-α、MDA、MPO含量增加,GSH含量下降(P<0。01);与CON组相比,LPS组MDA、Fe2+、ROS水平升高;CLP组肺组织和LPS组Beas-2B细胞TXNIP蛋白表达增加,TRX-1、GPX4及X-CT蛋白表达减低(P<0。01);与CLP组相比,CLP+Cur各浓度组肺损伤减轻,炎症因子和脂质过氧化因子含量降低,GSH水平升高;与LPS组相比,LPS+Cur各浓度组Fe2+、MDA和ROS水平下降(P<0。05);TXNIP蛋白表达降低,TRX-1、GPX4及X-CT蛋白表达增加(P<0。01)。PX-12干预后,取消了Cur对脓毒症肺组织和Beas-2B细胞的保护作用(P<0。05)。结论 姜黄素通过升高TRX-1、GPX4,降低TXNIP抑制铁死亡,减轻脓毒症肺损伤。
Curcumin alleviates septic lung injury in mice by inhibiting TXNIP/TRX-1/GPX4-mediated ferroptosis
Objective To investigate whether curcumin alleviates septic lung injury by inhibiting ferroptosis through modulating the TXNIP/TRX-1/GPX4 pathway.Methods Male C57BL/6 mice were randomly divided into Sham group,cecal ligation puncture(CLP)-induced sepsis group,CLP with curcumin treatment(50,100,and 200 mg/kg)groups,and CLP with both curcumin(200 mg/kg)and TRX-1 inhibitor PX-12(25 mg/kg)treatment group.Inflammatory factors,MDA,MPO,and GSH levels in the lung tissue of the mice were detected.Beas-2B cells stimulated with lipopolysaccharide(LPS;1 μg/mL)were treated with 2.5,5,or 10 μmol/L curcumin or with 10 μmol/L curcumin combined with 5 μmol/L PX-12,and the changes in MDA,Fe2+and ROS levels were assessed.Western blotting was performed to detect the protein expressions of TXNIP,TRX-1,GPX4 and X-CT in both the mouse lung tissues and Beas-2B cells.Results The mice with CLP-induced sepsis showed severe lung injury with elevated expressions of IL-6,IL-1β,TNF-α,MDA and MPO and decreased GSH expression.In Beas-2B cells,LPS stimulation significantly increased MDA and Fe2+levels and ROS release,increased TXNIP protein expression,and lowered the protein expression levels of TRX-1,GPX4 and X-CT,and these changes were also observed in the septic mice.Curcumin treatments at different concentrations obviously alleviated lung injury in the septic mice and reduced LPS-induced injury in Beas-2B cells.Curcumin significantly decreased the release of inflammatory factors,MDA and MPO,increased GSH level,lowered Fe2+,MDA and ROS levels,increased TXNIP protein expression,and lowered the protein expressions of TRX-1,GPX4 and X-CT in both septic mouse lung tissues and LPS-stimulated Beas-2B cells.The protective effect of curcumin was effectively blocked by PX-12 treatment.Conclusion Curcumin inhibits ferroptosis and alleviates septic lung injury in mice by elevating TRX-1 and GPX4 and decreasing TXNIP in the lung tissue.

sepsis lung injurycurcuminferroptosisTXNIP/TRX-1/GPX4 pathway

陈凯、孟兆菲、闵静婷、王佳慧、李正红、高琴、胡俊锋

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脓毒血症肺损伤 姜黄素 铁死亡 TXNIP/TRX-1/GPX4通路

2024

南方医科大学学报
南方医科大学

南方医科大学学报

CSTPCD北大核心
影响因子:1.654
ISSN:1673-4254
年,卷(期):2024.44(9)