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AE3介导的油茶皂甙在心肌细胞缺氧复氧损伤中的实验研究 被引量:1

SQS Conductor-AE3 Experimental Study In the A/R damage of Cardiac Muscles Cells
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摘要 目的:阐明油茶皂苷(SQS)所产生心肌保护作用与AE3蛋白的基因表达关系,方法:采用RNA i技术,在心肌细胞水平上建立AE3蛋白低表达、同时建立缺氧/复氧损伤(A/R)模型及SQS预适应模型;通过测定,心肌细胞的博动频律、细胞生存率以及细胞培养液中LDH的变化;同时检测心肌细胞中AE3 mRNA、AE3蛋白的表达变化,结果:SQS预处理能明显提高A/R损伤后细胞存活率,减少LDH的漏出,AE3 mRNA、AE3蛋白表达明显上调,与A/R组相比均有显著性差异(均p<0.01);结论:在心肌细胞中转导入三段有AE3基因序列特异性的dsRNA后,可引起AE3 mRNA及蛋白低表达,同时取消SQS预处理的心肌保护作用.为其进一步的新药开发提供理论与实验依据. Objective : indicating the relationship between the pretection function of cardiac muscles produced by sasanquqsaponin (SQS) and gene expression of AE3 protein. Methods: taking RNAi techniques, establishing AE3 protein low expression on the level of cardiac cells, as well as establishing the model of abscent oxygen/repair oxygen and the pre -adapted model of SQS; through different intervention, assaying the changes of throb frequency of cardiac muscles cell. existing rate of cells and LDH in the cell of cultivating fluid; meantime, assaying the expressing changes of AE3 mRNA. AE3 protein in the cardiac muscles cells. Results: pretreatment of SQS can improve livability of A/R damaged cells; reduce the leak of LDH; Protein expression of AE3 mRNA. AE3 are upgraded apparently. Comparing to group A/R, there is apparent change (all p 〈0. 01) ; Conclusion: conduct three sects dsRNA with the specialty of AE3 gene series into the cardiac cells, there will cause AE3 mRNA and protein low expression; meantime cancel the cardiac protection function of SQS pretreatment. In order to provide theories and experimental gist for further new drugs development.
出处 《宜春学院学报》 2006年第6期12-14,共3页 Journal of Yichun University
基金 江西省教育厅自然科学课题
关键词 油茶皂甙 A/R 预处理 RNAI技术 心肌细胞 Sasanquqsaponin (SQS) A/R damage Pretreatment RNAi techniques Cardiac muscles cells
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参考文献6

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