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Functional basis of associative learning and their relationships with long-term potentiation evoked in the involved neural circuits: Lessons from studies in behaving mammals

机译:联想学习的功能基础及其在涉及的神经回路中引起的长期增强的关系:来自行为哺乳动物的研究经验

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While contemporary neuroscience is paying increasing attention to subcellular and molecular events and other intracellular phenomena underlying the acquisition, storage, and retrieval of newly acquired motor and cognitive abilities, parallel attention should be paid to the study of the electrophysiological phenomena taking place at selected cortical and subcortical neuronal and synaptic sites during the precise moment of learning acquisition, extinction, and recall. These in vivo approaches to the study of learning and memory processes will allow the proper integration of the important information collected from in vitro and delayed molecular studies. Here, we summarize studies in behaving mammals carried out in our laboratory during the past ten years on the relationships between experimentally evoked long-term potentiation (LTP) and activity-dependent changes in synaptic strength taking place in hippocampal, prefrontal and related cortical and subcortical circuits during the acquisition of classical eyeblink conditioning or operant learning tasks. These studies suggest that different hippocampal synapses are selectively modified in strength during the acquisition of classical, but not instrumental, learning tasks. In contrast, selected prefrontal and striatum synapses are more directly modified by operant conditioning. These studies also show that besides N-methyl-D-aspartate (NMDA) receptors, many other neurotransmitter, intracellular mediating, and transcription factors participate in these two types of associative learning. Although experimentally evoked LTP seems to prevent the acquisition of classical eyeblink conditioning when induced at selected hippocampal synapses, it proved to be ineffective in preventing the acquisition of operant conditioned tasks when induced at numerous hippocampal, prefrontal, and striatal sites. The differential roles of these cortical structures during these two types of associative learning are discussed, and a diagrammatic representation of their respective functions is presented. (C) 2015 The Authors. Published by Elsevier Inc.
机译:当当代神经科学越来越关注亚细胞和分子事件以及其他新获得的运动和认知能力的获取,储存和恢复背后的细胞内现象时,应同时注意研究在选定皮层和大脑皮层发生的电生理现象。皮层下神经元和突触位点在学习习性,消亡和记忆的精确时刻。这些用于学习和记忆过程的体内方法将允许适当整合从体外和延迟分子研究中收集的重要信息。在这里,我们总结了过去十年来在实验室中进行的行为哺乳动物研究,这些研究涉及实验诱发的长期增强(LTP)与海马,前额叶及相关皮质和皮质下皮质发生的突触强度的活动依赖性变化之间的关系。采集经典眨眼条件或操作学习任务期间的电路。这些研究表明,不同的海马突触在学习经典而非学习性学习任务的过程中选择性地改变了强度。相反,选择的前额叶和纹状体突触可通过手术条件更直接地修饰。这些研究还表明,除了N-甲基-D-天冬氨酸(NMDA)受体外,许多其他神经递质,细胞内介导和转录因子也参与了这两种类型的联想学习。尽管在选定的海马突触中诱导诱发的LTP似乎阻止了经典眨眼条件的获得,但事实证明,在许多海马,前额叶和纹状体诱导时,LTP不能有效地阻止操作性条件任务的获得。讨论了这两种联想学习过程中这些皮质结构的不同作用,并给出了它们各自功能的示意图。 (C)2015作者。由Elsevier Inc.发布

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