Department of Neurology, Chongqing Key Laboratory of Neurology, The First Affiliated Hospital of Chongqing Medical University, Chongqing, 400016, China.
Mol Neurobiol. 2016 Sep;53(7):5013-24. doi: 10.1007/s12035-015-9431-8. Epub 2015 Sep 16.
Approximately 30 % of epilepsy cases are refractory to current pharmacological treatments through unknown mechanisms. Much work has been done on the role of synaptic components in the pathogenesis of epilepsy, but relatively little attention has been given to the potential role of the microtubules. We investigated the level of microtubule dynamic in 30 human epileptic tissues and two different chronic epilepsy rat models. The administration of microtubule-modulating agent attenuated the progression of chronic epilepsy. By contrast, microtubule-depolymerizing agent aggravated the progression of chronic epilepsy. The electrophysiological index by whole-cell clamp was used to investigate the neuronal excitation and inhibitory synaptic transmission in brain slices after administration of microtubule-modulating agent and microtubule-depolymerizing agent. Interestingly, we found that microtubule-modulating agent significantly increased the frequency of action potential firing in interneurons, and significantly promoted the amplitudes and frequencies of miniature inhibitory postsynaptic currents. Microtubule-depolymerizing agent had an opposite effect. These findings suggest that modulating hyperdynamic microtubules may take an anti-epileptic effect via postsynaptic mechanisms in interneurons. It could represent a potential pharmacologic target in epilepsy treatment.
大约 30%的癫痫病例由于未知机制对当前的药物治疗产生抗药性。许多工作已经研究了突触成分在癫痫发病机制中的作用,但相对较少关注微管的潜在作用。我们研究了 30 个人类癫痫组织和两种不同慢性癫痫大鼠模型中的微管动态水平。微管调节药物的给药减轻了慢性癫痫的进展。相比之下,微管解聚剂加重了慢性癫痫的进展。通过全细胞膜片钳技术,在给予微管调节药物和微管解聚剂后,研究脑片中神经元兴奋和抑制性突触传递的电生理指标。有趣的是,我们发现微管调节药物显著增加了中间神经元动作电位放电的频率,并显著促进了微小抑制性突触后电流的幅度和频率。微管解聚剂则产生相反的效果。这些发现表明,调节过度活跃的微管可能通过中间神经元的突触后机制产生抗癫痫作用。它可能成为癫痫治疗的一个潜在药物靶点。