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Memory and long-term potentiation (LTP) dissociated: Normal spatial memory despite CA1 LTP elimination with Kv1.4 antisense

机译:记忆和长期增强(LTP)分离:尽管使用Kv1.4反义消除了CA1 LTP,但正常的空间记忆

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摘要

Long-term potentiation (LTP) in the hippocampal slice preparation has been proposed as an in vitro model for long-term memory. However, correlation of LTP with memory in living animals has been difficult to demonstrate. Furthermore, in the last few years evidence has accumulated that dissociate the two. Because potassium channels might determine the weight of synapses in networks, we studied the role of Kv1.4, a presynaptic A-type voltage-dependent K+ channel, in both memory and LTP. Reverse transcription–PCR and Western blot analysis with specific antibodies showed that antisense oligodeoxyribonucleotide to Kv1.4 microinjected intraventricularly into rat brains obstructed hippocampal Kv1.4 mRNA, “knocking down” the protein in the hippocampus. This antisense knockdown had no effect on rat spatial maze learning, memory, or exploratory behavior, but eliminated both early- and late-phase LTP and reduced paired-pulse facilitation (a presynaptic effect) in CA1 pyramidal neurons without affecting dentate gyrus LTP. This presynaptic Kv1.4 knockdown together with previous postsynaptic Kv1.1 knockdown demonstrates that CA1 LTP is neither necessary nor sufficient for rat spatial memory.
机译:已经提出海马切片制剂中的长期增强(LTP)作为长期记忆的体外模型。然而,LTP与活体动物记忆的相关性很难证明。此外,在最近几年中,积累了使两者分离的证据。因为钾离子通道可能决定网络中突触的权重,所以我们研究了记忆和LTP中Kv1.4(突触前A型电压依赖性K +通道)的作用。逆转录PCR和特异抗体的Western印迹分析显示,脑室内注射Kv1.4的反义寡聚脱氧核糖核苷酸阻塞了海马Kv1.4 mRNA,“敲低”了海马中的蛋白质。这种反义敲低对大鼠空间迷宫的学习,记忆或探索行为没有影响,但消除了早期和晚期LTP并减少了CA1锥体神经元的成对脉冲促进作用(突触前作用),而不会影响齿状回LTP。这种突触前Kv1.4敲除与以前的突触后Kv1.1敲除一起证明,CA1 LTP对大鼠空间记忆既不是必需的也不是足够的。

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