Kovacs Peter, Hajnal Andras
Department of Neural and Behavioral Sciences, Pennsylvania State University, The Milton S. Hershey Medical Center, 500 University Drive, Hershey, PA 17033, USA.
Neuropeptides. 2009 Aug;43(4):283-93. doi: 10.1016/j.npep.2009.05.006. Epub 2009 Jun 21.
Brain insulin has widespread metabolic, neurotrophic, and neuromodulatory functions and is involved in the central regulation of food intake and body weight, learning and memory, neuronal development, neuronal apoptosis, and aging. To understand the neuromodulatory role of insulin, we aimed to characterize its yet undefined in vivo electrophysiological effects. We elected to record from the cerebellar cortex because this region has average insulin concentration and insulin receptor content in relation to the whole brain, and has been previously shown to be a target for insulin signaling. We used in vivo microiontophoresis to apply insulin juxtaneuronally while simultaneously recording changes in spontaneous neuronal activity. The analysis included 553 significant neuronal responses to insulin and other related agents recorded from 47 cerebellar neurons of the rat. We found that (1) insulin stimulation produced instant and reversible electrophysiological effects on all of the recorded neurons, and that (2) these effects were mostly dependent on prior or simultaneous GABA application (94-96%). Specifically, (a) inhibitory responses to insulin were the most common (58-62%), and were dose-dependent with respect to GABA pretreatments and blocked by co-administration of the insulin receptor inhibitor HNMPA. (b) In the second largest set of neurons (32-38%) insulin decreased the magnitude of GABA inhibitions when co-applied. (c) In contrast, only a small number of neurons showed GABA-independent responses to insulin application (4-6%), which were exclusively neuronal excitations. The present findings demonstrate that insulin has direct electrophysiological effects on central neurons in vivo and these effects are highly influenced by GABA-ergic inputs.
脑胰岛素具有广泛的代谢、神经营养和神经调节功能,参与食物摄入和体重、学习和记忆、神经元发育、神经元凋亡及衰老的中枢调节。为了解胰岛素的神经调节作用,我们旨在明确其尚未确定的体内电生理效应。我们选择从小脑皮质进行记录,因为该区域相对于全脑具有平均胰岛素浓度和胰岛素受体含量,且先前已被证明是胰岛素信号传导的靶点。我们采用体内微量离子电泳法在神经元旁施加胰岛素,同时记录自发神经元活动的变化。分析包括从大鼠47个小脑神经元记录到的553个对胰岛素及其他相关试剂的显著神经元反应。我们发现:(1)胰岛素刺激对所有记录的神经元产生即时且可逆的电生理效应;(2)这些效应大多依赖于预先或同时应用GABA(94 - 96%)。具体而言:(a)对胰岛素的抑制反应最为常见(58 - 62%),且在GABA预处理方面呈剂量依赖性,并可被胰岛素受体抑制剂HNMPA共同给药所阻断。(b)在第二大组神经元(32 - 38%)中,胰岛素与GABA共同应用时会降低GABA抑制的幅度。(c)相比之下,仅有少数神经元对胰岛素应用表现出不依赖GABA的反应(4 - 6%),且这些反应均为神经元兴奋。目前的研究结果表明,胰岛素在体内对中枢神经元具有直接电生理效应,且这些效应受GABA能输入的高度影响。