首页> 外文期刊>Brain research. Cognitive brain research >Phenytoin reverses the chronic stress-induced impairment of memory consolidation for water maze training and depression of LTP in rat hippocampal CA1 region, but does not affect motor activity.
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Phenytoin reverses the chronic stress-induced impairment of memory consolidation for water maze training and depression of LTP in rat hippocampal CA1 region, but does not affect motor activity.

机译:苯妥英钠逆转了慢性应激诱导的记忆障碍的损害,后者对于水迷宫训练和大鼠海马CA1区LTP抑制有抑制作用,但并不影响运动能力。

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Previous studies have shown that phenytoin can protect hippocampal structure from damage by chronic stress, while whether it can reverse the hippocampal malfunction induced by chronic stress is unknown. We investigated the effects of phenytoin on motor activity of stressed rats and on the long-term memory of water maze spatial training, which is known to depend on hippocampal function. We also explored whether phenytoin could protect long-term potentiation (LTP) in hippocampal CA1 region from depression of chronic stressed rats. Isolated hippocampal slices of rats were used to observe the changes of LTP in hippocampal CA1 field with electrophysiological technique. The results showed that the motor activity of chronic forced-swimming rats was markedly higher than that of control rats, and phenytoin could not affect this change. The performance of water maze spatial training indicated that chronic stress damages long-term memory but not short-term memory, and phenytoin could reverse this long-term memorydeficit. The increases of LTP after HFS in control and stress-phenytoin groups were significantly greater than those in stress-saline group (P < 0.05). There were no significant differences between control group and stress-phenytoin group (P > 0.05) and between control and control-phenytoin groups (P > 0.05). These findings provided the first evidence with behavioral and electrophysiological technique that phenytoin could reverse the hippocampal-dependent memory deficit and depression of LTP induced by chronic stress, which may be helpful for exploring the pathogenesis and improving the therapy of depression.
机译:先前的研究表明,苯妥英钠可以保护海马结构免受慢性应激的损害,而它是否能够逆转由慢性应激引起的海马功能障碍尚不清楚。我们调查了苯妥英钠对应激大鼠运动活动的影响以及对水迷宫空间训练的长期记忆的影响,而水迷宫空间训练的作用取决于海马功能。我们还探讨了苯妥英钠是否可以保护海马CA1区的长期增强(LTP)免受慢性应激大鼠抑郁的影响。分离大鼠海马切片,采用电生理技术观察海马CA1区LTP的变化。结果表明,慢性强迫游泳大鼠的运动活动明显高于对照组,苯妥英钠不能影响这一变化。水迷宫空间训练的性能表明,慢性应激会损害长期记忆,但不会损害短期记忆,并且苯妥英钠可以逆转这种长期记忆缺陷。对照组和应激苯妥英钠组HFS后LTP的增加明显大于应激盐水组(P <0.05)。对照组与应激苯妥英组之间无显着差异(P> 0.05),而对照组与对照组苯妥英组之间无显着差异(P> 0.05)。这些发现为行为和电生理技术提供了第一个证据,表明苯妥英钠可以逆转慢性应激引起的海马依赖性记忆缺陷和LTP抑制,这可能有助于探索其发病机理和改善抑郁症的治疗方法。

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