氧化应激通过抑制胱硫醚-γ-裂解酶介导阿霉素的心肌毒性
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广东省科技计划基金项目(2010B080701035;2008B080703053)


Oxidative Stress Mediates Doxorubicin-Induced Cardiotoxicity by Inhibiting Cystathionine-γ-Lyase
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    摘要:

    目的探讨氧化应激是否通过抑制胱硫醚-γ-裂解酶的表达及活性介导阿霉素的心肌毒性。方法应用阿霉素处理大鼠胚胎H9c2心肌细胞以建立阿霉素心肌毒性的细胞模型。在阿霉素处理前60 min用活性氧清除剂N-乙酰半胱氨酸预处理H9c2心肌细胞以观察氧化应激在阿霉素心肌细胞损伤中的作用。应用CCK-8检测心肌细胞存活率;双氯荧光素酶染色及荧光显微镜照相术检测细胞内活性氧水平;Western blot检测胱硫醚-γ-裂解酶的表达;亚甲基蓝显色法检测胱硫醚-γ-裂解酶活性。结果5μmol/L阿霉素处理H9c2细胞24 h引起明显的心肌毒性,使细胞存活率降低。阿霉素在促进细胞内活性氧生成的同时,还抑制胱硫醚-γ-裂解酶的表达及活性。N-乙酰半胱氨酸不仅抑制阿霉素对活性氧生成的促进作用,还减弱阿霉素的心肌毒性,并能阻断阿霉素对H9c2心肌细胞胱硫醚-γ-裂解酶表达及活性的抑制作用。结论活性氧可通过抑制心肌细胞胱硫醚-γ-裂解酶的表达及活性介导阿霉素的心肌毒性。

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    Aim To explore whether oxidative stress mediates doxorubicin-induced cardiotoxicity by inhibiting cystathionine-γ-lyase(CSE) expression and activity. Methods H9c2 cells treated with doxorubicin were used as the model of doxorubicin cardiototoxicity.H9c2 cells were pretreated with N-acetly-L-cysteine(NAC) 60 min prior to treatment with DOX so as to examine the role of oxidative stress in DOX-induced injury.Cell viability was measured by cell counter kit-8.The level of reactive oxygen species(ROS) was tested by dichlorfluorescein staining and photofluorography.Expression of CSE was detected by Western blot assay.Activity of CSE was examined by methylene blue test assay. Results Exposure of H9c2 cells to 5 μmol/L doxorubicin induced significant cardiotoxicity,leading to a decrease in cell viability.Doxorubicin not only enhanced ROS generation,but also inhibited CSE expression and activity in H9c2 cells.Pretreatment with NAC attenuated doxorubicin-induced ROS generation and cardiotoxicity,and also blocked the inhibitory effect of CSE expression and activity by doxorubicin. Conclusion ROS may mediate doxorubicin-induced cardiotoxicity by inhibiting CSE expression and activity.

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郑东诞,王秀玉,杨春涛,莫利求,兰爱平,胡芬,郭润民,沈宁,陈培熹,冯鉴强.氧化应激通过抑制胱硫醚-γ-裂解酶介导阿霉素的心肌毒性[J].中国动脉硬化杂志,2011,19(12):969~972.

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  • 收稿日期:2011-09-20
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