表征4-氨基吡啶诱导的癫痫样活性的浓度依赖性神经动力学。

Epilepsy journal Pub Date : 2018-01-01 Epub Date: 2018-06-28 DOI:10.4172/2472-0895.1000128
Timothy L Myers, Oscar C Gonzalez, Jacob B Stein, Maxim Bazhenov
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引用次数: 3

摘要

癫痫仍然是最常见的神经系统疾病之一。在患者中,其特征是无端、自发和反复发作或致命事件。通常,在癫痫发作之间可以测量到间期事件或人群水平的大发作,通常无症状。几十年的研究集中在了解导致癫痫样活动发展的机制,使用各种促惊厥药物,包括4-氨基吡啶(4AP)。然而,用于研究动物模型中4ap诱导的癫痫样活性的浓度缺乏一致性可能会导致结果及其解释的差异。事实上,在体内和体外研究中,4AP的浓度范围从3 μM到40 mM不等。在这里,我们探讨了不同浓度的4AP对急性小鼠大脑切片中海马癫痫样活动的发育和特征的影响。使用多电极阵列记录,我们发现4AP在广泛的浓度范围内诱导海马癫痫样活动。癫痫样活动的频率成分和时空模式显示出剂量依赖性反应。最后,在4AP存在的情况下,KCC2拮抗剂VU0240551降低KCC2共转运体活性,阻止了不同浓度4AP之间频率成分差异的表现。总体而言,该研究预测,不同浓度的4AP可导致海马癫痫样活动背后的不同机制,其中一些机制依赖于KCC2共转运体功能。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Characterizing Concentration-Dependent Neural Dynamics of 4-Aminopyridine-Induced Epileptiform Activity.

Characterizing Concentration-Dependent Neural Dynamics of 4-Aminopyridine-Induced Epileptiform Activity.

Characterizing Concentration-Dependent Neural Dynamics of 4-Aminopyridine-Induced Epileptiform Activity.

Characterizing Concentration-Dependent Neural Dynamics of 4-Aminopyridine-Induced Epileptiform Activity.

Epilepsy remains one of the most common neurological disorders. In patients, it is characterized by unprovoked, spontaneous, and recurrent seizures or ictal events. Typically, inter-ictal events or large bouts of population level activity can be measured between seizures and are generally asymptomatic. Decades of research have focused on understanding the mechanisms leading to the development of seizure-like activity using various pro-convulsive pharmacological agents, including 4-aimnopyridine (4AP). However, the lack of consistency in the concentrations used for studying 4AP-induced epileptiform activity in animal models may give rise to differences in results and interpretation thereof. Indeed, the range of 4AP concentration in both in vivo and in vitro studies varies from 3 μM to 40 mM. Here, we explored the effects of various 4AP concentrations on the development and characteristics of hippocampal epileptiform activity in acute mouse brain slices of either sex. Using multi-electrode array recordings, we show that 4AP induces hippocampal epileptiform activity for a broad range of concentrations. The frequency component and the spatiotemporal patterns of the epileptiform activity revealed a dose-dependent response. Finally, in the presence of 4AP, reduction of KCC2 co-transporter activity by KCC2 antagonist VU0240551 prevented the manifestation of the frequency component differences between different concentrations of 4AP. Overall, the study predicts that different concentrations of 4AP can result in the different mechanisms behind hippocampal epileptiform activity, of which some are dependent on the KCC2 co-transporter function.

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