Basic cellular and molecular mechanisms of refractory epilepsy: a review of current hypotheses

E. Viteva
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引用次数: 2

Abstract

Clarification of refractory epilepsy mechanisms is of great significance for its precise diagnosis and adequate therapeutic approach. This review presents current hypotheses of refractory epilepsy formation: 1. Hypothesis of genetic factors; 2. Hypothesis of multi-drug transporters; 3. Target hypothesis; 4. Hypothesis of mechanisms related to antiepileptic drugs – development of tolerance and ineffective mechanisms of action 5. Hypothesis of epilepsy related factors – seizure etiology, epilepsy progression, structural brain changes or neural net alterations. The latter hypothesis is closely related to the hypothesis of intrinsic severity as a determinant of antiepileptic drug resistance. A combination of mechanisms is also a possible explanation of refractoriness. Each of these hypotheses characterizes refractory epilepsy to a different extent without attaining an explicit and complex explanation of epileptogenesis.
难治性癫痫的基本细胞和分子机制:当前假说综述
阐明难治性癫痫的发病机制对其准确诊断和合理治疗具有重要意义。本文综述了目前关于难治性癫痫形成的假说:1。遗传因素假说;2. 多药物转运体假说;3.目标假设;4. 抗癫痫药物相关机制的假说——耐受性和无效作用机制的发展癫痫相关因素的假设——癫痫病因、癫痫进展、脑结构改变或神经网络改变。后一种假设与内在严重程度作为抗癫痫药物耐药性的决定因素的假设密切相关。多种机制的结合也可能是耐火的一种解释。每一种假说都在不同程度上描述了难治性癫痫,但对癫痫发生却没有一个明确而复杂的解释。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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