Hsu Mike S, Lee Darrin J, Binder Devin K
Epilepsy Research Laboratory, Department of Neurological Surgery, University of California, Irvine, USA.
Neuron Glia Biol. 2007 Nov;3(4):287-97. doi: 10.1017/S1740925X08000112.
Recent studies have implicated glial cells in novel physiological roles in the CNS, such as modulation of synaptic transmission, so it is possible that glial cells might have a functional role in the hyperexcitability that is characteristic of epilepsy. Indeed, alterations in distinct astrocyte membrane channels, receptors and transporters have all been associated with the epileptic state. This paper focuses on the potential roles of the glial water channel aquaporin-4 (AQP4) in modulating brain excitability and in epilepsy. We review studies of seizure phenotypes, K(+) homeostasis and extracellular space physiology of mice that lack AQP4 (AQP4(-/-) mice) and discuss the human studies demonstrating alterations of AQP4 in specimens of human epilepsy tissue. We conclude with new studies of AQP4 regulation by seizures and discuss its potential role in the development of epilepsy (epileptogenesis). Although many questions remain unanswered, the available data indicate that AQP4 and its molecular partners might represent important new therapeutic targets.
最近的研究表明,神经胶质细胞在中枢神经系统中具有新的生理作用,如调节突触传递,因此神经胶质细胞可能在癫痫所特有的过度兴奋中发挥功能性作用。事实上,不同的星形胶质细胞膜通道、受体和转运体的改变都与癫痫状态有关。本文重点探讨胶质水通道蛋白4(AQP4)在调节脑兴奋性和癫痫中的潜在作用。我们回顾了缺乏AQP4的小鼠(AQP4基因敲除小鼠)的癫痫发作表型、钾离子稳态和细胞外空间生理学的研究,并讨论了在人类癫痫组织标本中显示AQP4改变的人体研究。我们以癫痫发作对AQP4调节的新研究作为结尾,并讨论其在癫痫发生(癫痫形成)中的潜在作用。尽管许多问题仍未得到解答,但现有数据表明,AQP4及其分子伴侣可能代表重要的新治疗靶点。