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首页> 外文期刊>Brain research >Nefiracetam induces a long-lasting facilitation of hippocampal postsynaptic responses in mice lacking the NMDA receptor epsilon1 subunit.
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Nefiracetam induces a long-lasting facilitation of hippocampal postsynaptic responses in mice lacking the NMDA receptor epsilon1 subunit.

机译:奈非西坦可在缺乏NMDA受体epsilon1亚基的小鼠中长期促进海马突触后反应。

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摘要

The present study was designed to assess whether the facilitatory action of nefiracetam, a pyrrolidone derivative, on hippocampal postsynaptic responses is dependent upon N-methyl-D-aspartate (NMDA) receptors or not, by monitoring population spikes (PSs) in the dentate gyrus of hippocampal slices from mice lacking the NMDA receptor epsilon1 subunit. Nefiracetam (1 microM) induced a sustained facilitation of postsynaptic responses in the dentate gyrus of hippocampal slices from wild-type mice. The facilitation occluded the potentiation induced by high-frequency stimulation at the perforant path, and vice versa, suggesting a common mechanism between them. The perforant path long-term potentiation (LTP) was not induced in epsilon1 subunit knock-out mice, but nefiracetam (1 microM) persistently potentiated PS amplitude, reaching 280% of basal levels 50 min after 10-min treatment, similar to the potentiation achieved with wild-type mice. The results of the present study, thus, suggest that nefiracetam exerts its facilitatory action on hippocampal postsynaptic responses in an NMDA receptor-independent manner.
机译:本研究旨在通过监测齿状回中的种群尖峰(PS)来评估吡咯烷酮衍生物奈非西坦对海马突触后反应的促进作用是否依赖于N-甲基-D-天冬氨酸(NMDA)受体。缺少NMDA受体epsilon1亚基的小鼠的海马切片。 Nefiracetam(1 microM)在野生型小鼠海马切片的齿状回中持续促进突触后反应。促进作用阻碍了高频刺激在穿孔路径上引起的增强作用,反之亦然,表明它们之间存在共同的机制。在epsilon1亚基敲除小鼠中未诱导穿孔路径长期增强(LTP),但奈非西坦(1 microM)持续增强PS振幅,在治疗10分钟后50分钟达到基础水平的280%,类似于增强用野生型小鼠实现。因此,本研究的结果表明奈非西坦以不依赖NMDA受体的方式发挥其对海马突触后反应的促进作用。

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