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对皮质中突触可塑性的调节需要了解所有相关因素。

Modulation of Synaptic Plasticity in the Cortex Needs to Understand All the Players.

作者信息

Meunier Claire N J, Chameau Pascal, Fossier Philippe M

机构信息

Institut de Neurosciences Paris-Saclay (NeuroPSI), UMR 91197 CNRS-Université Paris-Saclay Paris, France.

Swammerdam Institute for Life Sciences, Center for NeuroScience, University of Amsterdam Amsterdam, Netherlands.

出版信息

Front Synaptic Neurosci. 2017 Feb 1;9:2. doi: 10.3389/fnsyn.2017.00002. eCollection 2017.

Abstract

The prefrontal cortex (PFC) is involved in cognitive tasks such as working memory, decision making, risk assessment and regulation of attention. These functions performed by the PFC are supposed to rely on rhythmic electrical activity generated by neuronal network oscillations determined by a precise balance between excitation and inhibition balance (E/I balance) resulting from the coordinated activities of recurrent excitation and feedback and feedforward inhibition. Functional alterations in PFC functions have been associated with cognitive deficits in several pathologies such as major depression, anxiety and schizophrenia. These pathological situations are correlated with alterations of different neurotransmitter systems (i.e., serotonin (5-HT), dopamine (DA), acetylcholine…) that result in alterations of the E/I balance. The aim of this review article is to cover the basic aspects of the regulation of the E/I balance as well as to highlight the importance of the complementarity role of several neurotransmitters in the modulation of the plasticity of excitatory and inhibitory synapses. We illustrate our purpose by recent findings that demonstrate that 5-HT and DA cooperate to regulate the plasticity of excitatory and inhibitory synapses targeting layer 5 pyramidal neurons (L5PyNs) of the PFC and to fine tune the E/I balance. Using a method based on the decomposition of the synaptic conductance into its excitatory and inhibitory components, we show that concomitant activation of D1-like receptors (D1Rs) and 5-HTRs, through a modulation of NMDA receptors, favors long term potentiation (LTP) of both excitation and inhibition and consequently does not modify the E/I balance. We also demonstrate that activation of D2-receptors requires functional 5-HTRs to shift the E-I balance towards more inhibition and to favor long term depression (LTD) of excitatory synapses through the activation of glycogen synthase kinase 3β (GSK3β). This cooperation between different neurotransmitters is particularly relevant in view of pathological situations in which alterations of one neurotransmitter system will also have consequences on the regulation of synaptic efficacy by other neurotransmitters. This opens up new perspectives in the development of therapeutic strategies for the pharmacological treatment of neuronal disorders.

摘要

前额叶皮质(PFC)参与诸如工作记忆、决策、风险评估和注意力调节等认知任务。PFC执行的这些功能被认为依赖于由神经网络振荡产生的节律性电活动,这种振荡由循环兴奋与反馈和前馈抑制的协同活动所决定的兴奋与抑制平衡(E/I平衡)的精确平衡所决定。PFC功能的改变与几种疾病(如重度抑郁症、焦虑症和精神分裂症)中的认知缺陷有关。这些病理情况与不同神经递质系统(即血清素(5-HT)、多巴胺(DA)、乙酰胆碱……)的改变相关,这些改变会导致E/I平衡的改变。这篇综述文章的目的是涵盖E/I平衡调节的基本方面,并强调几种神经递质在调节兴奋性和抑制性突触可塑性中的互补作用的重要性。我们通过最近的研究结果来说明我们的目的,这些结果表明5-HT和DA协同调节靶向PFC第5层锥体神经元(L5PyNs)的兴奋性和抑制性突触的可塑性,并微调E/I平衡。使用一种基于将突触电导分解为其兴奋性和抑制性成分的方法,我们表明,通过对NMDA受体的调节,D1样受体(D1Rs)和5-羟色胺受体(5-HTRs)的同时激活有利于兴奋和抑制的长期增强(LTP),因此不会改变E/I平衡。我们还证明,D2受体的激活需要功能性5-HTRs来将E-I平衡向更多抑制方向转变,并通过激活糖原合酶激酶3β(GSK3β)来促进兴奋性突触的长期抑制(LTD)。鉴于一种神经递质系统的改变也会对其他神经递质对突触效能的调节产生影响的病理情况,不同神经递质之间的这种协同作用尤为重要。这为神经疾病的药物治疗策略的开发开辟了新的前景。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/47b8/5285384/a8e760112b5b/fnsyn-09-00002-g0001.jpg

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