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Sinusoidal stimulation trains suppress epileptiform spikes induced by 4-AP in the rat hippocampal CA1 region in-vivo

机译:正弦刺激训练抑制在大鼠海马CA1区中4-AP诱导的癫痫尖刺诱导的癫痫刺激

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Deep brain stimulation (DBS) shows promises in the treatment of refractory epilepsy. Due to the complex causes of epilepsy, the mechanisms of DBS are still unclear. Depolarization block caused by the persistent excitation of neurons may be one of the possible mechanisms. To test the hypothesis, 4-aminopyridine (4-AP) was injected in rat hippocampal CA1 region in-vivo to induce epileptiform activity. Sinusoidal stimulation trains were applied to the afferent pathway (Schaffer collaterals) of CA1 region to suppress the epileptiform spikes. Results show that 2-min long trains of sinusoidal stimulation (50 Hz) decreased the firing rate of population spikes (PS) and decreased the PS amplitudes significantly. In addition, small positive sharp waves replaced PS activity during the periods of stimulation. A lower frequency sinusoidal stimulation (10 Hz) failed to decrease the firing rate of PS, but decreased the PS amplitudes significantly. These results suggest that stimulation trains of sinusoidal waves could suppress epileptiform spikes. Presumably, the stimulation with a high enough frequency might excite the downstream neurons persistently and elevate the membrane potentials continuously, thereby cause depolarization blocks in the neurons. The findings of the study provide insights in revealing the mechanisms of DBS, and have important implications to the clinical treatment of epilepsy.
机译:深脑刺激(DBS)显示了治疗难治性癫痫的承诺。由于癫痫的复杂原因,DBS的机制仍然不清楚。由神经元的持续激发引起的去极化块可以是可能的机制之一。为了测试假设,将4-氨基吡啶(4-AP)注入大鼠海马CA1区,以诱导癫痫均匀活性。将正弦刺激培训研入Ca1区域的传入途径(Schaffer侧侧)以抑制癫痫尖峰。结果表明,2分钟的正弦刺激(50Hz)的训练量减少了群体尖峰(PS)的烧制率,并显着降低了PS幅度。此外,在刺激期间,小的正尖波更换了PS活动。较低的频率正弦刺激(10Hz)未能降低PS的烧制率,但显着降低了PS幅度。这些结果表明,正弦波的刺激列车可以抑制癫痫尖峰。据推测,具有足够高的频率的刺激可能持续激发下游神经元并连续升高膜电位,从而导致神经元中的去极化块。该研究的调查结果提供了揭示DBS机制的见解,并对癫痫的临床治疗具有重要意义。

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