Department of Pediatrics, Division of Neurology, School of Medicine, University of Colorado Denver, Aurora, CO 80045, United States.
Neurosci Lett. 2011 Jun 27;497(3):218-22. doi: 10.1016/j.neulet.2011.02.052. Epub 2011 Mar 3.
γ-Aminobutyric acid (GABA) is the major inhibitory neurotransmitter in the brain. GABA(A) receptors are heteropentamers formed by assembly of multiple subunits that generate a wide array of receptors with particular distribution and pharmacological profiles. Malfunction of these receptors has been associated with the pathophysiology of epilepsy and contribute to an imbalance of excitatory and inhibitory neurotransmission. The process of epilepsy development (epileptogenesis) is associated with changes in the expression and function of a large number of gene products. One of the major challenges is to effectively determine which changes directly contribute to epilepsy development versus those that are compensatory or not involved in the pathology. Substantial evidence suggests that changes in the expression and function of GABA(A) receptors are involved in the pathogenesis of epilepsy. Identification of the mechanisms involved in GABA(A) receptor malfunction during epileptogenesis and the ability to reverse this malfunction are crucial steps towards definitively answering this question and developing specific and effective therapies.
γ-氨基丁酸(GABA)是大脑中主要的抑制性神经递质。GABA(A)受体是由多个亚基组成的异五聚体,产生具有特定分布和药理学特征的多种受体。这些受体的功能障碍与癫痫的病理生理学有关,并导致兴奋性和抑制性神经递质的失衡。癫痫发展的过程(癫痫发生)与大量基因产物的表达和功能变化有关。主要挑战之一是有效确定哪些变化直接导致癫痫发生,哪些是代偿性的,哪些与病理学无关。大量证据表明,GABA(A)受体表达和功能的变化与癫痫的发病机制有关。确定癫痫发生过程中 GABA(A)受体功能障碍的相关机制以及逆转这种功能障碍的能力是明确回答这个问题并开发特异性和有效的治疗方法的关键步骤。