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体内树突活动的抑制调节。

Inhibitory Regulation of Dendritic Activity in vivo.

机构信息

Institute for Physiology, University of Bern Bern, Switzerland.

出版信息

Front Neural Circuits. 2012 May 25;6:26. doi: 10.3389/fncir.2012.00026. eCollection 2012.

Abstract

The spatiotemporal control of neuronal excitability is fundamental to the inhibitory process. We now have a wealth of information about the active dendritic properties of cortical neurons including axonally generated sodium action potentials as well as local sodium spikelets generated in the dendrites, calcium plateau spikes, and NMDA spikes. All of these events have been shown to be highly modified by the spatiotemporal pattern of nearby inhibitory input which can drastically change the output firing mode of the neuron. This means that particular populations of interneurons embedded in the neocortical microcircuitry can more precisely control pyramidal cell output than has previously been thought. Furthermore, the output of any given neuron tends to feed back onto inhibitory circuits making the resultant network activity further dependent on inhibition. Network activity is therefore ultimately governed by the subcellular microcircuitry of the cortex and it is impossible to ignore the subcompartmentalization of inhibitory influence at the neuronal level in order to understand its effects at the network level. In this article, we summarize the inhibitory circuits that have been shown so far to act on specific dendritic compartments in vivo.

摘要

神经元兴奋性的时空控制是抑制过程的基础。我们现在已经掌握了大量关于皮质神经元的活跃树突特性的信息,包括轴突产生的钠动作电位,以及在树突中产生的局部钠棘波、钙峰棘波和 NMDA 棘波。所有这些事件都被证明受到附近抑制性输入的时空模式的高度调节,这种调节可以极大地改变神经元的输出放电模式。这意味着嵌入新皮质微电路中的特定中间神经元群体可以比以前认为的更精确地控制锥体神经元的输出。此外,任何给定神经元的输出往往会反馈到抑制性回路中,从而使网络活动进一步依赖于抑制。因此,网络活动最终由皮质的亚细胞微电路控制,为了理解其在网络水平上的影响,不可能忽略神经元水平上抑制影响的亚区化。在本文中,我们总结了迄今为止在体内作用于特定树突隔室的抑制性回路。

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