首页> 外文期刊>Molecular and Cellular Biochemistry: An International Journal for Chemical Biology >Postnatal zinc or paraquat administration increases paraquat or zinc-induced loss of dopaminergic neurons: insight into augmented neurodegeneration
【24h】

Postnatal zinc or paraquat administration increases paraquat or zinc-induced loss of dopaminergic neurons: insight into augmented neurodegeneration

机译:产后锌或百草枯给药增加了多巴胺能神经元的百草枯或锌诱导的失去损失:洞察增强神经变性

获取原文
获取原文并翻译 | 示例
       

摘要

Epidemiological evidences have shown an association of exposure to pesticides or heavy metals with increased incidences of Parkinson's disease (PD) in humans. Exposure to pesticides or metals during the decisive period of the brain development increases the susceptibility of dopaminergic neurons upon re-exposure in adult rodents. However, the effect of early life exposure to pesticide on the heavy metal-induced neurodegeneration or heavy metal on pesticide-induced neurodegeneration is not yet explored. The current study explored the effect of developmental exposure to zinc (Zn), a metal or paraquat (PQ), a pesticide on the nigrostriatal dopaminergic neurons of rats challenged to Zn or PQ during adulthood. Exposure of Zn or PQ during adulthood alone exhibited marked reduction in motor activities, striatal dopamine and metabolites, glutathione content and number of dopaminergic neurons. However, the levels of lipid peroxidation, protein carbonyls, superoxide dismutase activity, pro-inflammatory cytokines and 4-hydroxynonenal-protein adducts were increased. While the expression of vesicular monoamine transporter-2 and tyrosine hydroxylase were attenuated, dopamine transporter and microglial marker Iba-1 expression, activated microglia, nuclear factor-kappa B activation, mitochondrial cytochrome c release and caspase-3/9 activation were augmented following Zn or PQ exposure. Albeit postnatal alone exposure did not alter any of the studied parameters, the developmental administration of Zn/PQ in re-challenged adult rats produced more pronounced changes in the aforementioned variables as compared with adulthood Zn or PQ alone intoxicated animals. The results demonstrate that postnatal Zn/PQ intoxication dents the oxidative stress, inflammation, cell death and dopamine metabolism and storage regulating machineries, which speed up the toxicant-induced degeneration during adulthood.
机译:流行病学证据表明,随着帕金森病(PD)的含量增加,对杀虫剂或重金属接触的关联。在大脑发育的决定性期间接触农药或金属在成人啮齿动物在成人啮齿动物再暴露时增加了多巴胺能神经元的敏感性。然而,尚未探索早期生命暴露于农药对重金属诱导的神经变性或重金属的农药的影响。目前的研究探讨了发育暴露于锌(Zn),金属或百草枯(PQ)的影响,在成年期挑战Zn或PQ的大鼠硝基雌蕊多巴胺神经元的农药。单独的成年期间Zn或PQ的暴露表现出明显还原电动机活性,纹状体多巴胺和代谢物,谷胱甘肽含量和多巴胺能神经元数。然而,脂质过氧化,蛋白质羰基,超氧化物歧化酶活性,促炎细胞因子和4-羟基蛋白蛋白质加合物的水平增加。虽然衰减了凹凸单胺转运蛋白-2和酪氨酸羟化酶的表达,但在Zn之后增加了多巴胺转运蛋白和微脊髓标记物IBA-1表达,活化的小凝血瘤,核因子-Kappa活化,线粒体细胞色素C释放和Caspase-3/9活化。或pq曝光。虽然产后单独的暴露未改变任何研究的参数,与成年Zn或PQ单独陶醉的动物相比,在重新攻击成年大鼠中,在重新攻击成年大鼠中产生更明显的变量的变化。结果表明,产后Zn / PQ中毒凹陷氧化应激,炎症,细胞死亡和多巴胺代谢和储存调节机器,其在成年期间加速了毒性诱导的变性。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号