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Inhibitory Plasticity: From Molecules to Computation and Beyond

机译:抑制塑性:从分子到计算及更远

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摘要

Synaptic plasticity is the cellular and molecular counterpart of learning and memory and, since its first discovery, the analysis of the mechanisms underlying long-term changes of synaptic strength has been almost exclusively focused on excitatory connections. Conversely, inhibition was considered as a fixed controller of circuit excitability. Only recently, inhibitory networks were shown to be finely regulated by a wide number of mechanisms residing in their synaptic connections. Here, we review recent findings on the forms of inhibitory plasticity (IP) that have been discovered and characterized in different brain areas. In particular, we focus our attention on the molecular pathways involved in the induction and expression mechanisms leading to changes in synaptic efficacy, and we discuss, from the computational perspective, how IP can contribute to the emergence of functional properties of brain circuits.
机译:突触可塑性是学习和记忆的细胞和分子对应,并且自第一次发现以来,突触强度长期变化的机制分析几乎完全专注于兴奋性联系。相反,抑制被认为是电路兴奋性的固定控制器。据最近,仅示出了抑制网络,通过驻留在其突触连接中的广泛机制来细化。在这里,我们审查了最近关于已经发现和特征在不同脑区域的抑制塑性(IP)形式的发现。特别是,我们将注意力集中在诱导和表达机制中所涉及的分子途径,导致突触疗效变化,我们讨论了IP如何有助于脑电路脑电路功能特性的出现。

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