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首页> 外文期刊>CNS neuroscience & therapeutics. >Suppressing synchronous firing of epileptiform activity by high‐frequency stimulation of afferent fibers in rat hippocampus
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Suppressing synchronous firing of epileptiform activity by high‐frequency stimulation of afferent fibers in rat hippocampus

机译:通过大鼠海马传入纤维的高频刺激抑制癫痫型活性的同步射击

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Aims Deep brain stimulation (DBS) is a promising technology for treating epilepsy. However, the efficacy and underlying mechanisms of the high‐frequency stimulation (HFS) utilized by DBS to suppress epilepsy remain uncertain. Previous studies have shown that HFS can desynchronize the firing of neurons.?In this study, we investigated whether the desynchronization effects of HFS can suppress epileptiform events. Methods HFS trains with seconds of duration (short) and a minute of duration (long) were applied at the afferent fibers (ie, Schaffer collaterals) of the hippocampal CA1 region in anesthetized rats in vivo. The amplitude and the rate of population spikes (PS) appeared in the downstream of stimulation were calculated to evaluate the intensity of synchronized firing of neuronal populations between short and long HFS groups. A test of paired‐pulse depression (PPD) was used to assess the alteration of inhibitory neuronal circuits. Results The sustained stimulation of a 60‐s long HFS suppressed the afterdischarges that were induced by a 5‐s short HFS to impair the local inhibitions. During the sustained HFS, the mean PS amplitude reduced significantly and the burst firing decreased, while the amount of neuronal firing did not change significantly. The paired‐pulse tests showed that with a similar baseline level of small PS2/PS1 ratio indicating a strong PPD, the 5‐s HFS increased the PS2/PS1 ratio to a value that was significantly greater than the corresponding ratio during sustained HFS, indicating that the PPD impaired by a short HFS may be restored by a sustained HFS. Conclusions The sustained HFS can desynchronize the population firing of epileptiform activity and accelerate a recovery of inhibitions to create a balance between the excitation and the inhibition of local neuronal circuits. The study provides new clues for further understanding the mechanism of DBS and for advancing the clinical application of DBS in treating epilepsy.
机译:目的是深脑刺激(DBS)是一种治疗癫痫的有希望的技术。然而,DBS使用的高频刺激(HFS)抑制癫痫的疗效和潜在机制仍然不确定。之前的研究表明,HFS可以去同步神经元的烧制。本研究,我们研究了HFS的去同步效应是否可以抑制癫痫型事件。方法HFS捕获秒秒(短)和持续时间(长)分钟的HFS培训在体内麻醉的大鼠中的海马CA1区的传入纤维(即Schaffer侧侧)。计算群体穗状花序(PS)的幅度和率在刺激下游出现,以评价短期和长HFS组之间的神经元群的同步烧制强度。配对脉冲凹陷(PPD)的试验用于评估抑制神经元电路的改变。结果60-S长HFs的持续刺激抑制了5-S短HFS诱导的后收集,以损害局部抑制。在持续的HFS期间,平均ps幅度显着减少并且突发烧制减少,而神经元射击量并没有显着变化。配对脉冲测试表明,具有相似的基线水平的小PS2 / PS1比,指示强PPD的比例,5-S HF增加到PS2 / PS1的比率与持续HFS期间显着大于相应比率的值。通过持续的HFS可以恢复由短HFS损害的PPD。结论持续的HFS可以去同步癫痫型活性的人口烧制,并加速抑制的恢复,以在激发和局部神经元电路的抑制之间产生平衡。该研究提供了进一步理解DBS机制和推进DBS治疗癫痫的临床应用的新线索。

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