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颞叶癫痫大鼠模型中齿状回篮状细胞回路功能障碍

Dysfunction of the dentate basket cell circuit in a rat model of temporal lobe epilepsy.

作者信息

Zhang Wei, Buckmaster Paul S

机构信息

Department of Comparative Medicine, Stanford University, Stanford, California 94305-5342, USA.

出版信息

J Neurosci. 2009 Jun 17;29(24):7846-56. doi: 10.1523/JNEUROSCI.6199-08.2009.

Abstract

Temporal lobe epilepsy is common and difficult to treat. Reduced inhibition of dentate granule cells may contribute. Basket cells are important inhibitors of granule cells. Excitatory synaptic input to basket cells and unitary IPSCs (uIPSCs) from basket cells to granule cells were evaluated in hippocampal slices from a rat model of temporal lobe epilepsy. Basket cells were identified by electrophysiological and morphological criteria. Excitatory synaptic drive to basket cells, measured by mean charge transfer and frequency of miniature EPSCs, was significantly reduced after pilocarpine-induced status epilepticus and remained low in epileptic rats, despite mossy fiber sprouting. Paired recordings revealed higher failure rates and a trend toward lower amplitude uIPSCs at basket cell-to-granule cell synapses in epileptic rats. Higher failure rates were not attributable to excessive presynaptic inhibition of GABA release by activation of muscarinic acetylcholine or GABA(B) receptors. High-frequency trains of action potentials in basket cells generated uIPSCs in granule cells to evaluate readily releasable pool (RRP) size and resupply rate of recycling vesicles. Recycling rate was similar in control and epileptic rats. However, quantal size at basket cell-to-granule cell synapses was larger and RRP size smaller in epileptic rats. Therefore, in epileptic animals, basket cells receive less excitatory synaptic drive, their pools of readily releasable vesicles are smaller, and transmission failure at basket cell-to-granule cell synapses is increased. These findings suggest dysfunction of the dentate basket cell circuit could contribute to hyperexcitability and seizures.

摘要

颞叶癫痫很常见且难以治疗。齿状颗粒细胞抑制作用减弱可能是原因之一。篮状细胞是颗粒细胞的重要抑制性细胞。在颞叶癫痫大鼠模型的海马切片中,评估了篮状细胞的兴奋性突触输入以及篮状细胞到颗粒细胞的单突触抑制性突触后电流(uIPSCs)。通过电生理和形态学标准识别篮状细胞。通过平均电荷转移和微小兴奋性突触后电流(mEPSCs)频率测量的对篮状细胞的兴奋性突触驱动,在毛果芸香碱诱导的癫痫持续状态后显著降低,并且在癫痫大鼠中一直保持较低水平,尽管存在苔藓纤维发芽。配对记录显示,癫痫大鼠中篮状细胞到颗粒细胞突触处的uIPSCs失败率更高,且幅度有降低趋势。较高的失败率并非归因于毒蕈碱型乙酰胆碱或GABA(B)受体激活对GABA释放的过度突触前抑制。篮状细胞中的高频动作电位串在颗粒细胞中产生uIPSCs,以评估可快速释放池(RRP)大小和回收囊泡的再供应速率。对照大鼠和癫痫大鼠的回收率相似。然而,癫痫大鼠中篮状细胞到颗粒细胞突触处的量子大小更大,RRP大小更小。因此,在癫痫动物中,篮状细胞接受的兴奋性突触驱动更少,其可快速释放囊泡池更小,并且篮状细胞到颗粒细胞突触处的传递失败增加。这些发现表明齿状篮状细胞回路功能障碍可能导致兴奋性过高和癫痫发作。

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