Nakao Akito, Miki Takafumi, Shimono Ken, Oka Hiroaki, Numata Tomohiro, Kiyonaka Shigeki, Matsushita Kaori, Ogura Hiroo, Niidome Tetsuhiro, Noebels Jeffrey L, Wakamori Minoru, Imoto Keiji, Mori Yasuo
Department of Synthetic Chemistry and Biological Chemistry, Graduate School of Engineering, Kyoto University, Kyoto, 615-8510, Japan.
Pflugers Arch. 2015 Apr;467(4):737-52. doi: 10.1007/s00424-014-1555-6. Epub 2014 Jun 20.
Cholinergically induced network activity is a useful analogue of theta rhythms involved in memory processing or epileptiform activity in the hippocampus, providing a powerful tool to elucidate the mechanisms of synchrony in neuronal networks. In absence epilepsy, although its association with cognitive impairments has been reported, the mechanisms underlying hippocampal synchrony remain poorly investigated. Here we simultaneously recorded electrical activities from 64 sites in hippocampal slices of CaV2.1 Ca(2+) channel mutant tottering (tg) mice, a well-established mouse model of spontaneous absence epilepsy, to analyze the spatiotemporal pattern of cholinergically induced hippocampal network activity. The cholinergic agonist carbachol induced oscillatory discharges originating from the CA3 region. In tg/tg mice, this hippocampal network activity was characterized by enhanced occupancy of discharges of relatively high frequency (6-10 Hz) compared to the wild type. Pharmacological analyses of slices, patch clamp electrophysiological characterization of isolated neurons, and altered patterns of hippocampal GABAA receptor subunit and Cl(-) transporter messenger RNA (mRNA) transcript levels revealed that this abnormality is attributable to a developmental retardation of GABAergic inhibition caused by immature intracellular Cl(-) regulation. These results suggest that the inherited CaV2.1 Ca(2+) channel mutation leads to developmental abnormalities in Cl(-) transporter expression and GABAA receptor compositions in hippocampal neurons and that compromised maturation of GABAergic inhibition contributes to the abnormal synchrony in the hippocampus of tg absence epileptic mice.
胆碱能诱导的网络活动是参与记忆处理的θ节律或海马体癫痫样活动的有用类似物,为阐明神经元网络同步机制提供了强大工具。在失神癫痫中,尽管已报道其与认知障碍有关,但海马体同步的潜在机制仍研究不足。在此,我们同时记录了CaV2.1钙离子通道突变体蹒跚(tg)小鼠海马切片中64个位点的电活动,tg小鼠是一种成熟的自发性失神癫痫小鼠模型,以分析胆碱能诱导的海马网络活动的时空模式。胆碱能激动剂卡巴胆碱诱导源自CA3区域的振荡放电。与野生型相比,在tg/tg小鼠中,这种海马网络活动的特征是相对高频(6 - 10Hz)放电的占有率增加。对切片的药理学分析、分离神经元的膜片钳电生理特征以及海马GABAA受体亚基和Cl(-)转运体信使核糖核酸(mRNA)转录水平的改变模式表明,这种异常归因于细胞内Cl(-)调节不成熟导致的GABA能抑制发育迟缓。这些结果表明,遗传性CaV2.1钙离子通道突变导致海马神经元中Cl(-)转运体表达和GABAA受体组成的发育异常,并且GABA能抑制的成熟受损导致tg失神癫痫小鼠海马体中的异常同步。