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夏涛, 何平, 王爱国, 陈晓栋, 匡刚, 牛强, 郭丽娟, 黄南, 陈学敏. PBDE-47和PCB153染毒致大鼠神经毒性作用[J]. 中国公共卫生, 2009, 25(5): 564-566. DOI: 10.11847/zgggws2009-25-05-30
引用本文: 夏涛, 何平, 王爱国, 陈晓栋, 匡刚, 牛强, 郭丽娟, 黄南, 陈学敏. PBDE-47和PCB153染毒致大鼠神经毒性作用[J]. 中国公共卫生, 2009, 25(5): 564-566. DOI: 10.11847/zgggws2009-25-05-30
XIA Tao, HE Ping, WANG Ai-guo, . Combined neurotoxicity effect of PBDE-47 and PCB153 in SD rats[J]. Chinese Journal of Public Health, 2009, 25(5): 564-566. DOI: 10.11847/zgggws2009-25-05-30
Citation: XIA Tao, HE Ping, WANG Ai-guo, . Combined neurotoxicity effect of PBDE-47 and PCB153 in SD rats[J]. Chinese Journal of Public Health, 2009, 25(5): 564-566. DOI: 10.11847/zgggws2009-25-05-30

PBDE-47和PCB153染毒致大鼠神经毒性作用

Combined neurotoxicity effect of PBDE-47 and PCB153 in SD rats

  • 摘要: 目的探讨2,2',4,4'-四溴联苯醚(PBDE-47)和2,2',4,4',5,5'-六氯联苯(PCB153)单独或联合染毒对SD大鼠的神经毒性作用及其机制。方法出生第10 d的SD大鼠经一次性PBDE-471,5,10 mg/(kg·bw)和/或PCB1535 mg/(kg·bw)染毒,用Morris水迷宫试验观察2月龄大鼠空间学习、记忆能力;用实时荧光定量RT-PCR检测海马组织死亡相关蛋白激酶(DAPK)、X染色体连锁的凋亡抑制蛋白(XIAP)、含半胱氨酸的天冬氨酸酶-12(Caspase-12)、含半胱氨酸的天冬氨酸酶-3(Caspase-3)以及细胞色素(cytochrome C)等钙信号通路相关基因mRNA的表达水平。结果随PBDE-47染毒剂量的增加,大鼠学习、记忆能力呈现减退的趋势,且所有染毒剂量组与对照组比较差异均有统计学意义(P<0.05),PCB153可增加PBDE-47的神经毒性作用。与对照组比较,10 mg/(kg·bw)染毒组PBDE-47可导致雌雄大鼠XIAP基因mRNA表达水平显著下调(P<0.05),同时使雌雄大鼠Caspase-12、Caspase-13、Cytochrome C以及雄性大鼠DAPK基因mRNA表达水平显著上调(P<0.05)。除雌雄大鼠DAPK以及雌性大鼠Cyto-chrome基因外,PBDE-47和PCB153对雌雄大鼠其他各基因mRNA表达水平的影响具有交互作用(P<0.05)。结论PBDE-47可引起大鼠神经系统损伤,同时影响大鼠海马区钙信号诱导的凋亡相关基因mRNA表达水平,PCB153可增强PBDE-47的上述神经毒性作用。

     

    Abstract: ObjectiveTo investigate the combined neurotoxicity effect of 2, 2; 4, 4=tetrabromodiphenyl ethers(PBDE-47) and 2, 2; 4, 4; 5, 5=hexachlorobiphenyl (PCB 153) and its mechanism in SD rats.MethodsThe toxic SD rats models of PBDE-47 or/and PCB 153 were prepared by the treatment of different concentrations of PBDE-47(1, 5,10mg/kg·bw) or/and PCB 153 (5mg/kg·bw).The changes of spatial learning and memory ability of 2-month-old SD rats were investigated by the Morris watermaze experiment Then the mRNA expression levels of DAPK, XIAP, caspase-12, caspase-3, and cytochrome C in hippocampus of the rats were examined by real-time RT-PCR.ResultsWith the increase of PBDE-47 dose, the spatial learning and memory ability of the rats showed a trend of decline, and significant difference existed in all dose groups compared with the control(P<0.05).Meanwhile, PCB 153 could enhance the neurotoxic effects induced by PBDE-47.Comparedwith the control, the mRNA expression level of XlAP was significantly decreased (P<0.05),and them RNA expression levels of caspase-12, caspase-3, and cytochrome Cof male and female SD rats as well as the DAPK of male SD rats were increased in 10mg/kg·bw of PBDE-47 group(P<0.05).Except the DAPK of both male and female rats and the cytochrome Coffemale rats, the interaction between PBDE-47 and PCB 153 existed in the influence of mRNA expression level of other genes(P<0.05).ConclusionPBDE-47 could result in nervous system injury of SD rats, and influence the mRNA expression level of apoptotic pathway-associated genes induced by calcium signaling in hippocampus of SD rats PCR 153 could enhance the neurotoxic effects of PRDE-4Z.

     

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