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山东大学学报(医学版) ›› 2010, Vol. 48 ›› Issue (8): 32-.

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灰树花多糖对四氯化碳肝L-02细胞损伤的保护作用

王玉卓1,谢珊珊1,孙涛1,张道来1,孙庆济2,孙云帆3,冯玉新1,辛华1   

  1. 1.山东大学医学院细胞生物学研究所, 济南 250012; 2.济南澳利生物工程有限公司, 济南 250306;
    3.山东大学医学院, 济南 250012
  • 收稿日期:2010-03-17 出版日期:2010-08-16 发布日期:2010-08-16
  • 通讯作者: 辛华(1950- ),女,教授,主要从事细胞损伤与保护研究。 E-mail:xinhua@sdu.edu.cn
  • 作者简介:王玉卓(1978- ),男,硕士研究生,主要从事细胞生物学的研究。 E-mail:wyz-ok@hotmail.com
  • 基金资助:

    山东省中医药科技发展计划资助项目(2007-128)。

Inhibitory effect of the polysaccharide of Grifola frondosa on carbon tetrachloride-induced injury to liver cell line L-02

WANG Yu-zhuo1,  XIE Shan-shan 1, SUN Tao1, ZHANG Dao-lai1, SUN Qing-ji2, SUN Yun-fan3, FENG Yu-xin1, XIN Hua1   

  1. 1. Institute of Cell Biology, School of Medicine, Shandong University, Jinan 250012, China; 
    2. Aoli BioEngineering Company Limited, Jinan 250306, China; 
    3. School of Medicine, Shandong University, Jinan 250012, China
  • Received:2010-03-17 Online:2010-08-16 Published:2010-08-16

摘要:

目的    探讨灰树花多糖(PGF)对四氯化碳诱导的肝L-02细胞损伤的保护作用。 方法    培养人肝L-02细胞,建立CCl4肝细胞损伤模型,分组实验:正常对照组、CCl4损伤组和不同浓度的PGF(50 、100、200和400μg/mL)保护组。采用形态学观察,MTT检测,生化分析培养液中ALT、AST活性及细胞内SOD活性、MDA含量,流式细胞仪检测线粒体膜电位、荧光探针观测胞内Ca2+浓度;Western blot检测细胞bcl-2、bax蛋白表达。结果与CCl4损伤组相比,各PGF保护组细胞活力明显增强,上清液中ALT、AST活性明显降低; 细胞内SOD明显升高、Ca2+浓度MDA含量降低,细胞bcl-2的表达上调、 bax的表达下调。以100μg/mL浓度保护效果最佳。结论    PGF对CCl4诱导的肝L-02细胞损伤有明显的保护作用,其机制可能与清除自由基、抑制肝细胞内Ca2+浓度的升高、改变凋亡相关蛋白bcl-2、bax的表达水平,有效地防止线粒体膜电位的下降、减少细胞凋亡有关。

关键词: 灰树花多糖;肝损伤;凋亡

Abstract:

Objective    To investigate the inhibitory effect of the polysaccharide of grifola frondosa (PGF) on carbon tetrachloride (CCl4)-induced injury to liver cell line L-02.  Methods    Human liver cell line L-02 was cultured and the CCl4 -induced liver cell injury model was set up . The cells were divided into the normal control group, the CCl4-damaged group and the PGF inhibitory groups (50, 100, 200 and 400μg/mL). MTT assay was used and morphology was observed to measure cell activity. The contents of alanine aminotransferase (ALT) , aspartate aminotranferase (AST) , superoxide dismutase(SOD) and malondialdehyde (MDA) were detected. The changes of mitochondrial membrane potential of L-02 were analyzed by flow cytometry. The concentration of the intracellular calcium ion was determined by Fluo3-AM. Expressions of  bcl-2 and bax proteins were measured by Western blot analysis.  Results     Compared with the CCl4-damaged group, PGF improved the relative survival of L-02, lowered activities of the AST and ALT in medium, prevented the elevation of MDA, kept the high degree of SOD, prevented the decrease of the mitochondrial membrane potential and increase of the concentration of Ca2+,  up-regulated expression of bcl-2, and down-regulated expression of bax. PGF at a concentration of 100μg/mL had the best inhibitory effect. Conclusion    PGF can significantly prevent L-02 cells from damage induced by CCl4, and the mechanism may be related to scavenging free radicals, inhibiting  intracellular calcium overload, stabilizing mitochondrial membrane potential, and regulating expressions of bcl-2 and bax proteins.

Key words: Polysaccharide of Grifola frondosa; CCl4-induced hepaocyte injury; Apoptosis

中图分类号: 

  • Q952
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