Zhou Jun-Li, Lenck-Santini Pierre-Pascal, Zhao Qian, Holmes Gregory L
Neuroscience Center at Dartmouth, Section of Neurology, Dartmouth Medical School, Lebanon, New Hampshire, USA.
Epilepsia. 2007 Apr;48(4):720-31. doi: 10.1111/j.1528-1167.2006.00972.x. Epub 2007 Feb 5.
The interictal EEG spike(s) is the hallmark of the epileptic EEG. While focal interictal spike (IS) have been associated with transitory cognitive impairment, with the type of deficit dependent on where in the cortex the IS arises, the mechanism by which IS result in transitory dysfunction is not known. The purpose of this study was to determine the effect of IS on single-cell firing patterns in freely moving rats with a prior history of seizures.
We studied IS in two seizure models; pilocarpine-induced status epilepticus and recurrent flurothyl models. The effect of spontaneous hippocampal spikes on action potentials (APs) of CA1 cells in rats walking in a familiar environment was investigated using 32 extracellular electrodes. We also compared the effect of spikes on two types of hippcampal cells; place cells that discharge rapidly only when the rat's head is in a specific part of the environment, the so-called firing field, and interneurons, which are a main source of inhibition in the hippocampus.
IS were associated with a decreased likelihood of AP compared with IS-free portions of the record. Compared to pre-IS baseline, IS were followed by significant decreases in CA1 APs for periods up to 2 s following the IS in both models. When occurring in flurries, IS were associated with a pronounced decrease in APs. The response to IS was cell-dependent; IS resulted in decreases in AP firing after the IS in interneurons but not place cells.
This study demonstrates that IS have substantial effects on cellular firing in the hippocampus and that these effects last far longer than the spike and slow wave. Furthermore, the effect of IS on cellular firing was cell specific, affecting interneurons more than place cells. These findings suggest that IS may contribute to seizure-induced cognitive impairment by altering AP firing in a cell-specific manner.
发作间期脑电图棘波是癫痫性脑电图的标志。虽然局灶性发作间期棘波(IS)与短暂性认知障碍有关,且缺陷类型取决于IS在皮质的起源位置,但IS导致短暂性功能障碍的机制尚不清楚。本研究的目的是确定IS对有癫痫发作史的自由活动大鼠单细胞放电模式的影响。
我们在两种癫痫模型中研究IS;毛果芸香碱诱导的癫痫持续状态模型和反复戊四氮模型。使用32个细胞外电极,研究了在熟悉环境中行走的大鼠海马自发棘波对CA1细胞动作电位(AP)的影响。我们还比较了棘波对两种海马细胞的影响;位置细胞,仅在大鼠头部处于环境的特定部分(即所谓的放电场)时才快速放电,以及中间神经元,它们是海马中抑制的主要来源。
与记录中无IS的部分相比,IS与AP发生的可能性降低有关。与IS前基线相比,在两种模型中,IS后CA1区AP在长达2秒的时间内显著减少。当IS成群出现时,与AP的明显减少有关。对IS的反应具有细胞依赖性;IS导致中间神经元在IS后AP放电减少,但位置细胞没有。
本研究表明,IS对海马中的细胞放电有显著影响,且这些影响持续的时间远比棘波和慢波长得多。此外,IS对细胞放电的影响具有细胞特异性,对中间神经元的影响大于位置细胞。这些发现表明,IS可能通过以细胞特异性方式改变AP放电而导致癫痫发作引起的认知障碍。