Sensory Reinforced Corticostriatal Plasticity.

IF 4.8 2区 医学 Q1 NEUROSCIENCES Current Neuropharmacology Pub Date : 2024-01-01 DOI:10.2174/1570159X21666230801110359
Nicolas Vautrelle, Véronique Coizet, Mariana Leriche, Lionel Dahan, Jan M Schulz, Yan-Feng Zhang, Abdelhafid Zeghbib, Paul G Overton, Enrico Bracci, Peter Redgrave, John N J Reynolds
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Abstract

Background: Regional changes in corticostriatal transmission induced by phasic dopaminergic signals are an essential feature of the neural network responsible for instrumental reinforcement during discovery of an action. However, the timing of signals that are thought to contribute to the induction of corticostriatal plasticity is difficult to reconcile within the framework of behavioural reinforcement learning, because the reinforcer is normally delayed relative to the selection and execution of causally-related actions.

Objective: While recent studies have started to address the relevance of delayed reinforcement signals and their impact on corticostriatal processing, our objective was to establish a model in which a sensory reinforcer triggers appropriately delayed reinforcement signals relayed to the striatum via intact neuronal pathways and to investigate the effects on corticostriatal plasticity.

Methods: We measured corticostriatal plasticity with electrophysiological recordings using a light flash as a natural sensory reinforcer, and pharmacological manipulations were applied in an in vivo anesthetized rat model preparation.

Results: We demonstrate that the spiking of striatal neurons evoked by single-pulse stimulation of the motor cortex can be potentiated by a natural sensory reinforcer, operating through intact afferent pathways, with signal timing approximating that required for behavioural reinforcement. The pharmacological blockade of dopamine receptors attenuated the observed potentiation of corticostriatal neurotransmission.

Conclusion: This novel in vivo model of corticostriatal plasticity offers a behaviourally relevant framework to address the physiological, anatomical, cellular, and molecular bases of instrumental reinforcement learning.

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感官强化皮质突触可塑性
背景:相位多巴胺能信号诱导的皮层传导的区域性变化是发现动作过程中负责工具性强化的神经网络的一个基本特征。然而,被认为有助于诱导皮层可塑性的信号的时间很难在行为强化学习的框架内进行协调,因为强化物通常相对于因果相关行动的选择和执行是延迟的:虽然最近的研究已经开始探讨延迟强化信号的相关性及其对皮层可塑性处理的影响,但我们的目的是建立一个模型,在该模型中,感觉强化物会触发适当延迟的强化信号,并通过完整的神经元通路传递到纹状体,同时研究其对皮层可塑性的影响:方法:我们使用闪光作为自然感觉强化剂,通过电生理记录测量了大脑皮层的可塑性,并在体内麻醉大鼠模型制备中进行了药理操作:结果:我们证明了运动皮层单脉冲刺激所诱发的纹状体神经元尖峰激增可以通过完整的传入通路得到自然感觉强化剂的增强,信号时间与行为强化所需的时间近似。对多巴胺受体的药物阻断减弱了所观察到的皮层神经递质的增效作用:结论:这一新型体内皮质可塑性模型为研究工具强化学习的生理、解剖、细胞和分子基础提供了一个与行为相关的框架。
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来源期刊
Current Neuropharmacology
Current Neuropharmacology 医学-神经科学
CiteScore
8.70
自引率
1.90%
发文量
369
审稿时长
>12 weeks
期刊介绍: Current Neuropharmacology aims to provide current, comprehensive/mini reviews and guest edited issues of all areas of neuropharmacology and related matters of neuroscience. The reviews cover the fields of molecular, cellular, and systems/behavioural aspects of neuropharmacology and neuroscience. The journal serves as a comprehensive, multidisciplinary expert forum for neuropharmacologists and neuroscientists.
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