首页> 外文期刊>Journal of psychiatric research >Effects of mood stabilizers on oxidative stress-induced cell death signaling pathways in the brains of rats subjected to the ouabain-induced animal model of mania Mood stabilizers exert protective effects against ouabain-induced activation of the cell death pathway
【24h】

Effects of mood stabilizers on oxidative stress-induced cell death signaling pathways in the brains of rats subjected to the ouabain-induced animal model of mania Mood stabilizers exert protective effects against ouabain-induced activation of the cell death pathway

机译:情绪稳定剂对哇巴因诱导的躁狂症动物模型大鼠脑中氧化应激诱导的细胞死亡信号通路的影响情绪稳定剂对哇巴因诱导的细胞死亡通路的激活具有保护作用

获取原文
获取原文并翻译 | 示例
       

摘要

The present study aimed to investigate the effects of mood stabilizers, specifically lithium (Li) and valproate (VPA), on mitochondrial superoxide, lipid peroxidation, and proteins involved in cell death signaling pathways in the brains of rats subjected to the ouabain-induced animal model of mania. Wistar rats received Li, VPA, or saline twice a day for 13 days. On the 7th day of treatment, the animals received a single intracerebroventricular injection of ouabain or aCSF. After the ICV injection, the treatment with mood stabilizers continued for 6 additional days. The locomotor activity of rats was measured using the open-field test. In addition, we analyzed oxidative stress parameters, specifically levels of phosphorylated p53 (pp53), BAX and Bcl-2 in the brain of rats by immunoblot Li and VPA reversed ouabain-related hyperactivity. Ouabain decreased Bcl-2 levels and increased the oxidative stress parameters BAX and pp53 in the brains of rats. Li and VPA improved these ouabain-induced cellular dysfunctions; however, the effects of the mood stabilizers were dependent on the protein and brain region analyzed. These findings suggest that the Na+/K+-ATPase can be an important link between oxidative damage and the consequent reduction of neuronal and glial density, which are both observed in BD, and that Li and VPA exert protective effects against ouabain-induced activation of the apoptosis pathway. (C) 2015 Elsevier Ltd. All rights reserved.
机译:本研究旨在研究情绪稳定剂,特别是锂(Li)和丙戊酸盐(VPA),对哇巴因诱导的动物大脑中线粒体超氧化物,脂质过氧化和参与细胞死亡信号传导通路的蛋白质的影响躁狂症的模型。 Wistar大鼠每天两次接受Li,VPA或生理盐水,共13天。在治疗的第7天,动物接受脑室注射哇巴因或aCSF单次。注射ICV后,继续用情绪稳定剂治疗6天。使用开放视野测试测量大鼠的运动活性。此外,我们分析了氧化应激参数,特别是通过免疫印迹Li和VPA逆转的哇巴因相关的过度活跃症大鼠脑中的磷酸化p53(pp53),BAX和Bcl-2的水平。哇巴因降低了大鼠大脑中的Bcl-2水平,并增加了氧化应激参数BAX和pp53。 Li和VPA改善了哇巴因诱导的细胞功能障碍。但是,情绪稳定剂的作用取决于所分析的蛋白质和大脑区域。这些发现表明,Na + / K + -ATPase可能是氧化损伤与随之而来的神经元和神经胶质密度降低之间的重要联系,两者均在BD中观察到,并且Li和VPA对哇巴因诱导的神经元活化起保护作用。凋亡途径。 (C)2015 Elsevier Ltd.保留所有权利。

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