Department of Physiology, Medical College of Georgia, 1120 15th Street Augusta, GA 30912, USA.
J Physiol. 2011 Aug 15;589(Pt 16):3929-41. doi: 10.1113/jphysiol.2011.207340. Epub 2011 Jun 20.
Despite the long-established presence of glutamate NMDA receptors at extrasynaptic sites (eNMDARs), their functional roles remain poorly understood. Factors influencing the concentration and time course of glutamate in the extrasynaptic space, such as the topography of the neuronal–glial microenvironment, as well as glial glutamate transporters, are expected to affect eNMDAR-mediated signalling strength. In this study, we used in vitro and in vivo electrophysiological recordings to assess the properties, functional relevance and modulation of a persistent excitatory current mediated by activation of eNMDARs in hypothalamic supraoptic nucleus (SON) neurons. We found that ambient glutamate of a non-synaptic origin activates eNMDARs to mediate a persistent excitatory current (termed tonic I(NMDA)), which tonically stimulates neuronal activity. Pharmacological blockade of GLT1 astrocyte glutamate transporters, as well as the gliotoxin α-aminodadipic acid, enhanced tonic I(NMDA) and neuronal activity, supporting an astrocyte regulation of tonic I(NMDA) strength. Dehydration, a physiological challenge known to increase SON firing activity and to induce neuroglial remodelling, including reduced neuronal ensheathment by astrocyte processes, resulted in blunted GLT1 efficacy, enhanced tonic I(NMDA) strength, and increased neuronal activity. Taken together, our studies support the view that glial modulation of tonic I(NMDA) activation contributes to regulation of SON neuronal activity, contributing in turn to neuronal homeostatic responses during a physiological challenge.
尽管谷氨酸 NMDA 受体在突触外部位(eNMDARs)的存在由来已久,但它们的功能作用仍知之甚少。影响突触外空间中谷氨酸浓度和时程的因素,如神经元-神经胶质微环境的拓扑结构以及神经胶质谷氨酸转运体,预计会影响 eNMDAR 介导的信号转导强度。在这项研究中,我们使用体外和体内电生理记录来评估下丘脑视上核(SON)神经元中 eNMDAR 激活介导的持续兴奋性电流的特性、功能相关性和调节。我们发现,非突触来源的环境谷氨酸激活 eNMDAR 以介导持续的兴奋性电流(称为 tonic I(NMDA)),该电流持续刺激神经元活动。GLT1 星形胶质细胞谷氨酸转运体的药理学阻断以及神经胶质毒素 α-氨基己二酸,增强了 tonic I(NMDA)和神经元活性,支持 tonic I(NMDA)强度的星形胶质细胞调节。脱水是一种已知会增加 SON 放电活动并诱导神经胶质重塑的生理挑战,包括星形胶质细胞过程对神经元包绕的减少,导致 GLT1 功效降低、tonic I(NMDA)强度增强和神经元活性增加。总之,我们的研究支持这样一种观点,即胶质细胞对 tonic I(NMDA)激活的调节有助于调节 SON 神经元活动,进而有助于在生理挑战期间神经元的稳态反应。