Raimondo Joseph V, Dulla Chris
Epilepsy Curr. 2019 Jul-Aug;19(4):256-257. doi: 10.1177/1535759719853548. Epub 2019 Jun 4.
Magloire, V., Cornford, J., Lieb, A., Kullmann, D. M., and Pavlov, I. . 10, 1225. doi:10.1038/s41467-019-08933-4. Although cortical interneurons are apparently well-placed to suppress seizures, several recent reports have highlighted a paradoxical role of perisomatic-targeting parvalbumin-positive (PV+) interneurons in ictogenesis. Here, we use an acute in vivo model of focal cortical seizures in awake behaving mice, together with closed-loop optogenetic manipulation of PV+ interneurons, to investigate their function during seizures. We show that photo-depolarization of PV+ interneurons rapidly switches from an anti-ictal to a pro-ictal effect within a few seconds of seizure initiation. The pro-ictal effect of delayed photostimulation of PV+ interneurons was not shared with dendrite-targeting somatostatin-positive (SOM+) interneurons. We also show that this switch can be prevented by overexpression of the neuronal potassium-chloride co-transporter KCC2 in principal cortical neurons. These results suggest that strategies aimed at improving the ability of principal neurons to maintain a trans-membrane chloride gradient in the face of excessive network activity can prevent interneurons from contributing to seizure perpetuation.
马格洛雷,V.,康福德,J.,利布,A.,库尔曼,D.M.,以及帕夫洛夫,I. 10, 1225。doi:10.1038/s41467-019-08933-4。尽管皮质中间神经元似乎处于很好的抑制癫痫发作的位置,但最近的几份报告强调了靶向胞体的小白蛋白阳性(PV+)中间神经元在癫痫发作产生中具有矛盾的作用。在这里,我们使用清醒行为小鼠局灶性皮质癫痫发作的急性体内模型,结合对PV+中间神经元的闭环光遗传学操纵,来研究它们在癫痫发作期间的功能。我们表明,在癫痫发作开始后的几秒钟内,PV+中间神经元的光去极化迅速从抗癫痫作用转变为促癫痫作用。对PV+中间神经元延迟光刺激的促癫痫作用并不适用于靶向树突的生长抑素阳性(SOM+)中间神经元。我们还表明,这种转变可以通过在主要皮质神经元中过表达神经元钾氯共转运体KCC2来预防。这些结果表明,旨在提高主要神经元在面对过度网络活动时维持跨膜氯梯度能力的策略,可以防止中间神经元促成癫痫发作的持续。