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A Biophysical Model of Synaptic Plasticity and Metaplasticity Can Account for the Dynamics of the Backward Shift of Hippocampal Place Fields

机译:突触可塑性和可塑性的生物物理模型可以解释海马位场向后移动的动力学

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摘要

Hippocampal place cells in the rat undergo experience-dependent changes when the rat runs stereotyped routes. One such change, the backward shift of the place field center of mass, has been linked by previous modeling efforts to spike-timing–dependent plasticity (STDP). However, these models did not account for the termination of the place field shift and they were based on an abstract implementation of STDP that ignores many of the features found in cortical plasticity. Here, instead of the abstract STDP model, we use a calcium-dependent plasticity (CaDP) learning rule that can account for many of the observed properties of cortical plasticity. We use the CaDP learning rule in combination with a model of metaplasticity to simulate place field dynamics. Without any major changes to the parameters of the original model, the present simulations account both for the initial rapid place field shift and for the subsequent slowing down of this shift. These results suggest that the CaDP model captures the essence of a general cortical mechanism of synaptic plasticity, which may underlie numerous forms of synaptic plasticity observed both in vivo and in vitro.
机译:当大鼠运行定型路线时,大鼠中的海马位置细胞会经历依赖于经验的变化。一种这样的变化,即位置场重心的向后偏移,已被以前的建模工作与依赖于峰值定时的可塑性(STDP)联系在一起。但是,这些模型并未考虑到位置场偏移的终止,它们基于STDP的抽象实现而忽略了皮质可塑性中的许多特征。在这里,代替抽象的STDP模型,我们使用依赖于钙的可塑性(CaDP)学习规则,该规则可以解释皮层可塑性的许多观察特性。我们将CaDP学习规则与可塑性模型结合使用,以模拟场所动态。在没有对原始模型的参数进行任何重大更改的情况下,当前的仿真既考虑了初始快速放置场偏移,又考虑了随后该偏移的减慢。这些结果表明,CaDP模型捕获了突触可塑性的一般皮质机制的实质,这可能是在体内和体外观察到的多种形式的突触可塑性的基础。

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