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NMDAR-independent hippocampal long-term depression impairment after status epilepticus in a lithium-pilocarpine model of temporal lobe epilepsy

机译:在颞叶癫痫锂 - 汲取碳粉模型中的状态癫痫术后NMDAR独立的海马长期抑郁症

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摘要

Temporal lobe epilepsy is usually associated with cognitive decline and memory deficits. Despite numerous existing studies on various animal models, the mechanisms of these deficits remain largely unclear. A specific form of long-term synaptic efficacy changeslong-term depression (LTD)is thought to play an important role in memory formation and learning. However, extremely little is known about the possible alteration of LTD induction and dynamics after a status epilepticus (SE). In this work, we investigated the acute and delayed effects of lithium-pilocarpine-induced SE on NMDAR-dependent and NMDAR-independent hippocampal LTD in vitro. We found that SE affected the NMDAR-dependent and NMDAR-independent forms of LTD in different manners. The NMDAR-dependent form of LTD was almost intact 3 days after SE, but it switched from a predominantly presynaptic to a more postsynaptic locus of expression. In contrast, the NMDAR-independent LTD in the hippocampal Schaffer collaterals-CA1 synapses was fully abolished 3 days after SE. Our results emphasize the role of non-NMDA-dependent synaptic plasticity changes in the processes of epileptogenesis and the potential for therapy development.
机译:颞叶癫痫通常与认知下降和记忆缺陷相关联。尽管对各种动物模型进行了许多现有研究,但这些赤字的机制仍然很大程度上不清楚。一种特定形式的长期突触疗效变化延长(LTD)被认为在记忆形成和学习中发挥着重要作用。然而,在状态癫痫(SE)后,有限公司可能改变的可能改变极少。在这项工作中,我们研究了锂毒性野兔诱导的SE在肌肌的急性和延迟效应,在体外依赖NMDAR依赖性和NMDAR的海马有限公司。我们发现SE影响了不同举止的NMDAR依赖性和NMDAR独立的有限公司。 NMDAR依赖形式的LTD在SE后3天几乎完好无损,但它从主要的预先突触前转换为更大的表达突触轨迹。相比之下,在SE后3天完全废除了海马Schaffer胶胶中的Nmdar独立有限公司。我们的结果强调了非NMDA依赖性突触可塑性变化在癫痫发生过程中的作用和治疗发育的潜力。

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