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Cell domain-dependent changes in the glutamatergic and GABAergic drives during epileptogenesis in the rat CA1 region

机译:大鼠CA1区癫痫发生过程中谷氨酸能和GABA能驱动的细胞结构域依赖性变化

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摘要

An increased ratio of the glutamatergic drive to the overall glutamatergic/GABAergic drive characterizes the chronic stage of temporal lobe epilepsy (TLE), but it is unclear whether this modification is present during the latent period that often precedes the epileptic stage. Using the pilocarpine model of TLE in rats, we report that this ratio is decreased in hippocampal CA1 pyramidal cells during the early phase of the latent period (3–5 days post pilocarpine). It is, however, increased during the late phase of the latent period (7–10 days post pilocarpine), via cell domain-dependent alterations in synaptic current properties, concomitant with the occurrence of interictal-like activity in vivo. During the late latent period, the glutamatergic drive was increased in somata via an enhancement in EPSC decay time constant and in dendrites via an increase in EPSC frequency and amplitude. The GABAergic drive remained unchanged in the soma but was decreased in dendrites, since the drop off in IPSC frequency was more marked than the increase in IPSC kinetics. Theoretical considerations suggest that these modifications are sufficient to produce interictal-like activity. In epileptic animals, the ratio of the glutamatergic drive to the overall synaptic drive was not further modified, despite additional changes in synaptic current frequency and kinetics. These results show that the global changes to more glutamatergic and less GABAergic activities in the CA1 region precede the chronic stage of epilepsy, possibly facilitating the occurrence and/or the propagation of interictal activity.
机译:谷氨酸能驱动与总体谷氨酸能/ GABA能驱动的比率增加是颞叶癫痫(TLE)的慢性阶段的特征,但是尚不清楚这种改变是否在通常早于癫痫阶段的潜伏期中存在。使用TLE的毛果芸香碱模型,我们报道在潜伏期的早期(毛果芸香碱后3-5天),海马CA1锥体细胞的这一比例降低。然而,在潜伏期的后期(毛果芸香碱后7-10天),通过体内突触电流特性的细胞域依赖性变化,伴随体内类似间质活性的发生,其增加。在潜伏期后期,谷氨酸能驱动通过EPSC衰减时间常数的增加而在躯体中增加,而树突则通过EPSC频率和振幅的增加而增加。由于IPSC频率的下降比IPSC动力学的增加更明显,因此GABA能驱动在体细胞中保持不变,但在树突中下降。理论上的考虑表明,这些修饰足以产生类似间质的活性。在癫痫动物中,尽管突触电流频率和动力学发生了其他变化,但谷氨酸能驱动与总体突触驱动的比率并未进一步改变。这些结果表明,在癫痫的慢性期之前,CA1区更多的谷氨酸能活动和较少的GABA能活动发生了全局变化,这可能促进了发作间活动的发生和/或传播。

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