Protective effect of lipopolysaccharide pretreatment on cardiomyocytes anoxia/reoxygenation injury

刘丹; 尹东; 汤蕾; 孙惦; 许旻; 何明

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Protective effect of lipopolysaccharide pretreatment on cardiomyocytes anoxia/reoxygenation injury

更新时间：2026-01-09

- Protective effect of lipopolysaccharide pretreatment on cardiomyocytes anoxia/reoxygenation injury
- Journal of Army Medical University Vol. 34, Issue 17, Pages: 1707-1710(2012)
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  CLC： R394-33;R394.2;R542.2
- Published：2012
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刘丹,尹东,汤蕾,孙惦,许旻,何明.LPS预处理对心肌细胞缺氧/复氧损伤的保护作用[J].陆军军医大学学报(原第三军医大学学报),2012,34(17):1707-1710.

　Liu Dan,Yin Dong,Tang Lei,Sun Dian,Xu Ming,He Ming.Protective effect of lipopolysaccharide pretreatment on cardiomyocytes anoxia/reoxygenation injury[J].J Amry Med Univ (J Third Mil Med Univ),2012,34(17):1707-1710.
刘丹,尹东,汤蕾,孙惦,许旻,何明.LPS预处理对心肌细胞缺氧/复氧损伤的保护作用[J].陆军军医大学学报(原第三军医大学学报),2012,34(17):1707-1710. DOI：

　Liu Dan,Yin Dong,Tang Lei,Sun Dian,Xu Ming,He Ming.Protective effect of lipopolysaccharide pretreatment on cardiomyocytes anoxia/reoxygenation injury[J].J Amry Med Univ (J Third Mil Med Univ),2012,34(17):1707-1710. DOI：

摘要

目的探讨14-3-3γ基因在LPS预处理对抗心肌细胞缺氧/复氧（A/R）损伤中的作用。方法构建pSUPER/14-3-3γ RNA干扰重组质粒，转染入心肌细胞，分为5组：对照组、A/R组、LPS+A/R组、pSUPER+LPS+A/R组、pSUPER/14-3-3γ+LPS+A/R组。Western blot检测14-3-3γ蛋白表达，生化自动分析仪测定乳酸脱氢酶（LDH）活性，MTT法测定细胞存活率，流式细胞仪检测细胞凋亡，线粒体肿胀实验检测线粒体通透性转换孔（mPTP）开放。结果 A/R损伤使细胞存活率下降，LDH升高，细胞凋亡增加，mPTP开放；LPS预处理可使14-3-3γ表达明显增加，通过抑制mPTP开放，对A/R损伤的细胞有保护作用；pSUPER/14-3-3γ RNA干扰重组质粒通过抑制14-3-3γ蛋白表达，取消LPS预处理的保护作用。结论 LPS预处理可对抗心肌细胞缺氧/复氧损伤，其机制与上调14-3-3γ，从而抑制mPTP开放有关。

Abstract

Objective To explore the role of 14-3-3γ gene in the protection of cardiomyocytes with lipopolysaccharide (LPS) pretreatment against anoxia/reoxygenation (A/R) injury. Methods A RNA interference (RNAi) recombinant plasmid of pSUPER/14-3-3γ was constructed and transferred into cardiomyocytes. The cardiomyocytes were divided into five groups including a control group

an A/R group

a LPS+A/R group

a pSUPER+LPS+A/R group and a pSUPER/14-3-3γ+LPS+A/R group. The protein level of 14-3-3γ was detected by Western blotting. The activity of lactate dehydrogenase (LDH) was determined by an automated biochemical analyzer. Cell viability was analyzed by MTT assay. Cell apoptosis was measured by flow cytometry. The opening of mitochondrial permeability transition pore (mPTP) was determined by swelling of isolated cardiac mitochondria. Results The A/R damage resulted in cell viability decrease

LDH and cell apoptosis increase

and mPTP opening. The LPS pretreatment up-regulated 14-3-3γ protein expression and protected cardiomyocytes against A/R injury through inhibiting the mPTP opening. The pSUPER/14-3-3γ RNAi recombinant plasmid could reduce 14-3-3γ protein expression and then reverse the protective effect of LPS pretreatment. Conclusion LPS pretreatment may have a protective effect on cardiomyocytes subjected to A/R injury

and its mechanism may be related to 14-3-3γ upregulation and subsequent mPTP opening inhibition.

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