首页> 外文期刊>Biological trace element research >Effects of selenium and topiramate on lipid peroxidation and antioxidant vitamin levels in blood of pentylentetrazol-induced epileptic rats.
【24h】

Effects of selenium and topiramate on lipid peroxidation and antioxidant vitamin levels in blood of pentylentetrazol-induced epileptic rats.

机译:硒和托吡酯对戊四氮致癫痫大鼠血液脂质过氧化和抗氧化维生素水平的影响。

获取原文
获取原文并翻译 | 示例
       

摘要

Free radicals and selenium (Se) deficiency are involved in pathogenesis of epilepsy. Topiramate (TPM), a new anticonvulsant, was reported to possess neuroprotective effect via inhibition of free radicals. We investigated the effects of Se and TPM on pentylentetrazol (PTZ)-induced blood toxicity in rats. Forty male Wistar rats were equally divided into five groups. First and second groups were used as control and PTZ group, respectively. TPM and Se were administrated to rats constituting third and forth groups for 7 days, respectively. The TPM and Se combination were given to animals in fifth group for 7 days. At the end of 7 days all groups except the first group received single dose PTZ. The brain cortex samples were taken at 3 h of PTZ administration. PTZ resulted in significant increase in plasma and erythrocytes lipid peroxidation (LP) levels although plasma vitamin E concentrations and erythrocytes glutathione peroxidase (GSH-Px) activities were reduced by PTZ. The plasma and erythrocytes LP levels in third, fourth, and fifth groups were decreased as compared to second group although GSH-Px and reduced glutathione values increased in the groups. Vitamin C and E concentrations were increased through fourth and fifth group only. Vitamin A concentrations were not changed by PTZ. In conclusion, Se and TPM seem to have protective effects on the PTZ-induced blood toxicity by inhibiting free radical supporting antioxidant redox system.
机译:自由基和硒缺乏症与癫痫的发病机制有关。据报道,一种新型的抗惊厥药托吡酯(TPM)通过抑制自由基具有神经保护作用。我们调查了硒和TPM对戊四氮(PTZ)诱导的大鼠血液毒性的影响。将四十只雄性Wistar大鼠平均分为五组。第一组和第二组分别用作对照组和PTZ组。将TPM和Se分别给予组成第三和第四组的大鼠7天。将TPM和Se组合给予第五组动物7天。在7天结束时,除第一组外,所有组均接受单剂量PTZ。在PTZ给药3小时后采集大脑皮质样品。尽管PTZ降低了血浆维生素E浓度和红细胞谷胱甘肽过氧化物酶(GSH-Px)活性,但PTZ导致血浆和红细胞脂质过氧化(LP)水平显着增加。与第二组相比,第三,第四和第五组的血浆和红细胞LP水平降低,尽管各组中的GSH-Px和降低的谷胱甘肽值增加。仅第四和第五组维生素C和E的浓度增加。 PTZ不会改变维生素A的浓度。总之,Se和TPM似乎通过抑制自由基支持的抗氧化还原系统对PTZ诱导的血液毒性具有保护作用。

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