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丹参酮ⅡA抑制波动性高糖诱导的雪旺细胞凋亡的观察

来自:中国糖尿病杂志  编辑:孙连庆 王煊 李晓瑾等|点击数:|2016-02-26

 

【摘要】 目的  观察丹参酮ATanA)对波动性高糖(IHG)所致的雪旺细胞(SC)凋亡的影响。  方法  原代培养大鼠SC分为正常糖组(Con5.6 mmol/L)、稳定性高糖组(HG50 mmol/L)、IHG组(IHG5.650 mmol/L)、渗透压对照组(mannitolIHG加不同浓度TanA(0.1110 μmol/L)组。检测线粒体膜电位(MMP)、细胞凋亡率及凋亡相关蛋白表达。  结果  Con组和HG组比较,IHGMMP[0.51±0.02)vs1.42±0.08vs0.66±0.02],细胞凋亡率增高[(42.33±2.76)% vs31.64±3.04% vs (5.01±0.26)%](P0.05P0.01);线粒体细胞色素ccyto-c)及凋亡诱导因子(AIF)水平降低,胞浆cyto-c及胞核凋亡诱导因子(AIF)表达增高(P0.01);活化半胱天冬氨酸蛋白酶-9caspase-9)及caspase-3表达增高(P0.01)。  结论  TanA能抑制SC凋亡,其机制是caspase活性降低,从caspase依赖性及非依赖性途径发挥作用。

【关键词】  丹参酮A;波动性高糖;雪旺细胞;凋亡;凋亡诱导因子

        【Abstract  Objective  To investigate the effectinfluence of tanshinone IIA (Tan IIA) on sSchwann cells (SCs) apoptosis induced by intermittent high glucose (IHG).  Methods   SCs from primary cultured rats were divided into seven groups: SCs with normal glucose of 5.6mmol/L (Con group)SCs with high glucose of 50mmol/L (HG group), SCs with intermittent high glucose of 5.6-50mmol/L (IHG group), mannitol group, and IHG plus different concentrations of with Tan IIA ( of 0.1 μmol/L, 1 μmol/L, and 10 μmol/L) groups. Mitochondrial transmembrane potential (MMP), apoptosis rate and the expression levels of apoptosis-related proteins were determined in all groups.  Results   As compared with Con and HG groups, MMP was lower (1.42±0.08 vs 0.66±0.02 vs 0.51±0.02),  apoptosis rate was higher (5.01±0.26% vs 31.64±3.04% vs 42.33±2.76%) (P0.05 or P0.01) in IHG group., The expression levels of cytochrome c (cyto-c) and apoptosis inducing factor (AIF) in mitochondria decreasedwere lower, but the expression levels of cytoplasmic cyto-c and nuclear AIF in cytoplasm and nucleus were higherincreased (P0.01) in IHG group., and  The expression levels of activated caspase-9 and caspase-3 were higher (p<0.01) in IHG group.  Conclusion  Tan may reduce the activity of caspase through caspase-dependent and -independent pathway, thereby protect SCs from apoptosis.  

Key words  Tanshinone A (Tan A); Intermittent high glucose (IHG); Schwann cells(SCs); Apoptosis; Apoptosis inducing factor (AIF)

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