首页> 外文期刊>Drug and Chemical Toxicology >Memory enhancing effect of Nigella Sativa hydro-alcoholic extract on lipopolysaccharide-induced memory impairment in rats
【24h】

Memory enhancing effect of Nigella Sativa hydro-alcoholic extract on lipopolysaccharide-induced memory impairment in rats

机译:Nigella sativa水解提取物对大鼠脂多糖诱导的记忆障碍的记忆增强

获取原文
获取原文并翻译 | 示例
           

摘要

In this study, the effects of Nigella Sativa (NS) hydro-alcoholic extract on lipopolysaccharide (LPS)-induced learning and memory impairments, hippocampal cytokine levels, and brain tissues oxidative damage were investigated in rats. The rats were grouped and treated: (1) control (saline), (2) LPS (1 mg/ kg i.p.), and (3-5) 100, 200, or 400mg/kg NS hydro-alcoholic extract 30min before LPS injection. The treatment was started since 6 days before the behavioral experiments and continued during the behavioral tests (LPS injection 2 h before each behavioral experiment). Finally, the brains were removed for biochemical assessments. In Morris water maze (MWM) test, LPS increased the escape latency and traveled path compared to control group, whereas all doses of NS hydro-alcoholic extract decreased them compared to LPS group. In passive avoidance (PA) test, the latency to enter the dark compartment in LPS group was shorter than control group while in all treated groups it was longer than LPS group. LPS increased tumor necrosis factor-ac (TNF-a), interleukin-6 (IL-6), malondialdehyde (MDA), and nitric oxide (NO) metabolites, and decreased thiol content, superoxide dismutase (SOD), and catalase (CAT) in the hippocampal tissues compared to control group while NS hydro-alcoholic extract decreased MDA and NO metabolites and increased thiol content, SOD, and CAT compared to LPS group. Findings of the current study indicated that the hydro-alcoholic extract of NS improved the LPS-induced learning and memory impairments induced by LPS in rats by improving hippocampal cytokine levels and brain tissues oxidative damage.
机译:在这项研究中,在大鼠中研究了大鼠脂肪系(NS)水 - 酒精提取物对脂多糖(LPS)引起的学习和记忆障碍,海马细胞因子水平和脑组织氧化损伤的影响。将大鼠分组并处理:(1)对照(盐水),(2)LPS(1mg / kg IP),(3​​-5)100,200或400mg / kg NS水 - 酒精萃取物30min在LPS注射之前。自行为实验前6天开始并在行为试验期间继续进行治疗(在每个行为实验之前的LPS注射2小时)。最后,将脑袋除去生物化学评估。在Morris水迷宫(MWM)试验中,与对照组相比,LPS增加了逃逸延迟和行进路径,而所有剂量的NS水 - 酒精提取物与LPS组相比降低。在被动避免(PA)测试中,在LPS组中进入暗隔室的延迟比对照组短,而在所有处理的组中,它比LPS组长。 LPS增加肿瘤坏死因子-AC(TNF-A),白细胞介素-6(IL-6),丙二醛(MDA)和一氧化氮(NO)代谢物,降低硫醇含量,超氧化物歧化酶(SOD)和过氧化酯酶(猫)与对照组相比,与对照组相比,与LPS组相比,NS水性醇提取物降低,并且没有代谢物,SOD和CAT增加。目前研究的结果表明,通过改善海马细胞因子水平和脑组织氧化损伤,NS的氢酒醇提取物改善了LPS诱导的LPS诱导的学习和记忆障碍。

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