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关于联想学习的生理学和解剖学研究:与 W.T. Greenough 的学习研究的融合。

Physiological and anatomical studies of associative learning: Convergence with learning studies of W.T. Greenough.

机构信息

Department of Psychology, Beckman Institute for Advanced Science and Technology, University of Illinois at Urbana-Champaign, USA.

出版信息

Dev Psychobiol. 2011 Jul;53(5):489-504. doi: 10.1002/dev.20554.

DOI:10.1002/dev.20554
PMID:21678397
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3632307/
Abstract

The quest to understand how the brain is able to store information for later retrieval has been pursued by many scientists through the years. Although many have made very significant contributions to the field and our current understanding of the process, few have played as pivotal a role in advancing our understanding as William T. Greenough. The current report will utilize associative learning, a training paradigm that has greatly assisted in our understanding of memory consolidation, to demonstrate how findings emerging from the Greenough laboratory helped to not only shape our current understanding of learning induced anatomical plasticity, but to also launch future analyses into the molecular players involved in this process, especially the Fragile X Mental Retardation Protein.

摘要

多年来,许多科学家一直在探索大脑如何存储信息以备后用。尽管许多人对该领域做出了非常重大的贡献,并且我们目前对这一过程的理解也有所加深,但在推动我们对记忆巩固的理解方面,几乎没有人能像威廉·T·格林诺那样起到关键作用。本报告将利用联想学习,这一训练范例极大地帮助我们理解了记忆巩固,来展示格林诺实验室的研究结果不仅如何帮助我们塑造了目前对学习诱导的解剖可塑性的理解,而且还为这一过程中涉及的分子参与者,特别是脆性 X 智力迟钝蛋白的未来分析奠定了基础。

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本文引用的文献

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Senescent synapses and hippocampal circuit dynamics.衰老突触和海马体电路动态。
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Synapse distribution suggests a two-stage model of dendritic integration in CA1 pyramidal neurons.突触分布表明CA1锥体神经元树突整合的两阶段模型。
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Learning-related postburst afterhyperpolarization reduction in CA1 pyramidal neurons is mediated by protein kinase A.CA1锥体神经元中与学习相关的爆发后超极化减少由蛋白激酶A介导。
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