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首页> 外文期刊>Neuropharmacology >Changes in excitatory and inhibitory receptor expression and network activity during induction and establishment of epilepsy in the rat Reduced Intensity Status Epilepticus (RISE) model
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Changes in excitatory and inhibitory receptor expression and network activity during induction and establishment of epilepsy in the rat Reduced Intensity Status Epilepticus (RISE) model

机译:在诱导和建立大鼠癫痫期间兴奋性和抑制受体表达和网络活性的变化降低强度状态癫痫患者(崛起)模型

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The RISE model is an effective system to study the underlying molecular and cellular mechanisms involved in the initiation and maintenance of epilepsy in vivo. Here we profiled the expression of excitatory and inhibitory neurotransmitter receptor subunits and synaptic scaffolding proteins in the hippocampus and temporal lobe and compared these changes with alterations in network activity at specific timepoints during epileptogenesis. Significant changes occurred in all of the ionotropic glutamate receptor subunits tested during epilepsy induction and progression and the profile of these changes differed between the hippocampus and temporal lobe. Notably, AMPAR subunits were dramatically decreased during the latent phase of epilepsy induction, matched by a profound decrease in the network response to kainate application in the hippocampus. Moreover, decreases in the GABA(A)beta 3 subunit are consistent with a loss of inhibitory input contributing to the perturbation of excitatory/inhibitory balance and seizure generation. These data highlight the synaptic reorganisation that mediates the relative hypoexcitability prior to the manifestation of seizures and subsequent hyperexcitability when spontaneous seizures develop. These patterns of changes give new insight into the mechanisms underpinning epilepsy and provide a platform for future investigations targeting particular receptor subunits to reduce or prevent seizures.
机译:上升模型是研究癫痫中癫痫患者的潜在分子和细胞机制的有效系统。在这里,我们探讨了海马和颞叶中的兴奋性和抑制神经递质受体亚基和突触支架蛋白的表达,并将这些变化与癫痫发生期间特定的时间点的网络活性的改变进行了比较。在癫痫诱导和进展期间测试的所有离子型谷氨酸受体亚基发生显着变化,这些变化的轮廓不同于海马和颞叶。值得注意的是,在癫痫诱导的潜在阶段,AMPAR亚基在潜伏期阶段急剧下降,通过对海马的Kinate应用的网络反应进行了深远的降低匹配。此外,GABA(A)β3亚基的降低与抑制投入的丧失造成促进兴奋性/抑制性平衡和癫痫发作的扰动。这些数据突出了突触重组,在自发癫痫发作时在癫痫发作和随后的过度兴奋剂之前介导相对脱氧性的突触重组。这些变化模式对支撑癫痫的机制提供了新的洞察力,并为未来调查提供了针对特定受体亚基的未来调查的平台,以减少或预防癫痫发作。

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