Endocannabinoïdes et NeuroAdaptation, NeuroCentre Magendie INSERM U862, Bordeaux, France.
Front Neuroendocrinol. 2011 Jan;32(1):25-42. doi: 10.1016/j.yfrne.2010.07.004. Epub 2010 Jul 18.
There is overwhelming evidence for multiple effects of stress on excitatory transmission and synaptic plasticity in the hippocampus. These interactions between stress and hippocampal glutamatergic neurons play a role in the cognitive and emotional consequences of aversive stimuli. Stress impacts on excitatory synapses are mediated by a complex set of neurohormones and neurotransmitters, among which corticosteroid hormones secreted from the adrenal cortex play a crucial role. Most effects of corticosteroid hormones are mediated by their binding to cytosolic mineralocorticoid (MR) and glucocorticoid receptors (GR), which after translocation to the nucleus, regulate the transcription of target genes. Recent electrophysiological and live imaging experiments have however provided experimental data which reinforce the hypothesis that beside these delayed effects, corticosteroid hormones may also act rapidly through membrane receptors. The first goal of this review is to detail the tonic and intrinsic effects of corticosteroid hormones on hippocampal excitatory transmission, glutamate receptor trafficking and expression, and synaptic plasticity, paying attention to their temporality (rapid and transient effects followed by slow and persistent genomic effects). Its second goal is to dissect the extent to which acute/repeated stress influences hippocampal excitatory synapses and whether these are accounted for by corticosteroid hormones.
有大量证据表明,压力对海马体中的兴奋性传递和突触可塑性有多种影响。这些压力与海马体谷氨酸能神经元之间的相互作用,在厌恶刺激的认知和情绪后果中发挥作用。应激对兴奋性突触的影响是由一系列复杂的神经激素和神经递质介导的,其中肾上腺皮质分泌的皮质类固醇激素起着关键作用。皮质类固醇激素的大多数作用都是通过与细胞质中的盐皮质激素 (MR) 和糖皮质激素受体 (GR) 结合来介导的,这些受体在转位到细胞核后,调节靶基因的转录。然而,最近的电生理学和活体成像实验提供了实验数据,这些数据强化了这样一种假设,即除了这些延迟效应之外,皮质类固醇激素还可能通过膜受体迅速发挥作用。这篇综述的第一个目标是详细描述皮质类固醇激素对海马体兴奋性传递、谷氨酸受体转运和表达以及突触可塑性的紧张和内在作用,同时注意它们的时效性(快速和短暂的效应,随后是缓慢和持久的基因组效应)。其第二个目标是剖析急性/重复应激如何影响海马体兴奋性突触,以及这些影响是否归因于皮质类固醇激素。