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癫痫中齿状回篮状细胞大麻素敏感异型抑制的功能减退:对网络节律的影响

Functional Reduction in Cannabinoid-Sensitive Heterotypic Inhibition of Dentate Basket Cells in Epilepsy: Impact on Network Rhythms.

作者信息

Yu Jiandong, Proddutur Archana, Swietek Bogumila, Elgammal Fatima S, Santhakumar Vijayalakshmi

机构信息

Center for Neuropsychiatric Diseases, Institute of Life Science, Nanchang University, Nanchang 330031, China Department of Pharmacology, Physiology, and Neuroscience, Rutgers New Jersey Medical School, Newark, NJ 07103, USA.

Department of Pharmacology, Physiology, and Neuroscience, Rutgers New Jersey Medical School, Newark, NJ 07103, USA.

出版信息

Cereb Cortex. 2016 Oct 17;26(11):4229-4314. doi: 10.1093/cercor/bhv199. Epub 2015 Sep 22.

Abstract

Strong perisomatic inhibition by fast-spiking basket cells (FS-BCs) regulates dentate throughput. Homotypic FS-BC interconnections that support gamma oscillations, and heterotypic inputs from diverse groups of interneurons that receive extensive neurochemical regulation, together, shape FS-BC activity patterns. However, whether seizures precipitate functional changes in inhibitory networks and contribute to abnormal network activity in epilepsy is not known. In the first recordings from dentate interneuronal pairs in a model of temporal lobe epilepsy, we demonstrate that status epilepticus (SE) selectively compromises GABA release at synapses from dentate accommodating interneurons (AC-INs) to FS-BCs, while efficacy of homotypic FS-BC synapses is unaltered. The functional decrease in heterotypic cannabinoid receptor type 1 (CBR)-sensitive inhibition of FS-BCs resulted from enhanced baseline GABA-mediated suppression of synaptic release after SE. The frequency of CBR-sensitive inhibitory synaptic events in FS-BCs was depressed early after SE induction and remained reduced in epileptic rats. In biologically based simulations of heterogeneous inhibitory networks and excitatory-inhibitory cell networks, experimentally identified decrease in reliability of AC-IN to FS-BCs synaptic release reduced theta power and theta-gamma coupling and enhanced gamma coherence. Thus, the experimentally identified functional reduction in heterotypic inhibition of FS-BCs can contribute to compromised network oscillations in epilepsy and could precipitate memory and cognitive co-morbidities.

摘要

快速放电篮状细胞(FS-BCs)产生的强烈胞体周围抑制作用调节着齿状回的信息通量。支持γ振荡的同型FS-BC相互连接,以及来自接受广泛神经化学调节的不同中间神经元群体的异型输入,共同塑造了FS-BC的活动模式。然而,癫痫发作是否会促使抑制性网络发生功能变化并导致癫痫中异常的网络活动尚不清楚。在颞叶癫痫模型中首次对齿状回中间神经元对进行记录时,我们发现癫痫持续状态(SE)选择性损害了齿状回适应性中间神经元(AC-INs)到FS-BCs突触处的GABA释放,而同型FS-BC突触的效能未改变。FS-BCs的异型大麻素1型受体(CBR)敏感抑制作用的功能下降是由于SE后基线GABA介导的突触释放抑制增强所致。SE诱导后早期,FS-BCs中CBR敏感抑制性突触事件的频率降低,并且在癫痫大鼠中持续降低。在基于生物学的异质性抑制网络和兴奋性-抑制性细胞网络模拟中,实验确定的AC-IN到FS-BCs突触释放可靠性降低会降低θ功率和θ-γ耦合,并增强γ相干性。因此,实验确定的FS-BCs异型抑制作用的功能降低可能导致癫痫中网络振荡受损,并可能引发记忆和认知共病。

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