Losi Gabriele, Cammarota Mario, Carmignoto Giorgio
Institute of Neuroscience of the National Research Council and Department of Biomedical Sciences, University of Padova Padova, Italy.
Front Pharmacol. 2012 Jul 12;3:132. doi: 10.3389/fphar.2012.00132. eCollection 2012.
Epilepsies comprise a family of multifactorial neurological disorders that affect at least 50 million people worldwide. Despite a long history of neurobiological and clinical studies the mechanisms that lead the brain network to a hyperexcitable state and to the intense, massive neuronal discharges reflecting a seizure episode are only partially defined. Most epilepsies of genetic origin are related to mutations in ionic channels that cause neuronal hyperexcitability. However, idiopathic epilepsies of unclear origin represent the majority of these brain disorders. A large body of evidence suggests that in the epileptic brain neurons are not the only players. Indeed, the glial cell astrocyte is known to be morphologically and functionally altered in different types of epilepsy. Although it is unclear whether these astrocyte dysfunctions can have a causative role in epileptogenesis, the hypothesis that astrocytes contribute to epileptiform activities recently received a considerable experimental support. Notably, currently used antiepileptic drugs, that act mainly on neuronal ion channels, are ineffective in a large group of patients. Clarifying astrocyte functions in the epileptic brain tissue could unveil astrocytes as novel therapeutic targets. In this review we present first a short overview on the role of astrocytes in the epileptic brain starting from the "historical" observations on their fundamental modulation of brain homeostasis, such as the control of water content, ionic equilibrium, and neurotransmitters concentrations. We then focus our review on most recent studies that hint at a distinct contribution of these cells in the generation of focal epileptiform activities.
癫痫是一类多因素导致的神经系统疾病,全球至少有5000万人受其影响。尽管神经生物学和临床研究历史悠久,但导致脑网络进入高度兴奋状态并引发反映癫痫发作的强烈、大量神经元放电的机制仍未完全明确。大多数遗传性癫痫与导致神经元过度兴奋的离子通道突变有关。然而,病因不明的特发性癫痫占这些脑部疾病的大多数。大量证据表明,在癫痫脑中,神经元并非唯一的参与者。事实上,已知胶质细胞星形胶质细胞在不同类型的癫痫中会发生形态和功能改变。虽然尚不清楚这些星形胶质细胞功能障碍是否在癫痫发生中起因果作用,但星形胶质细胞促成癫痫样活动的假说最近得到了大量实验支持。值得注意的是,目前使用的主要作用于神经元离子通道的抗癫痫药物,对很大一部分患者无效。阐明癫痫脑组织中星形胶质细胞的功能可能会揭示星形胶质细胞作为新的治疗靶点。在这篇综述中,我们首先简要概述星形胶质细胞在癫痫脑中的作用,从关于它们对脑内环境稳态的基本调节(如水含量、离子平衡和神经递质浓度的控制)的“历史”观察开始。然后,我们将综述重点放在最近的研究上,这些研究暗示了这些细胞在局灶性癫痫样活动产生中的独特作用。