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Hebb 式条件作用增强活体皮层刺激的检测阈值。

Enhanced detection threshold for in vivo cortical stimulation produced by Hebbian conditioning.

机构信息

Department of Physiology, Feinberg School of Medicine, Northwestern University, 303 E. Chicago Ave., Chicago, IL 60611, USA.

出版信息

J Neural Eng. 2011 Feb;8(1):016011. doi: 10.1088/1741-2560/8/1/016011. Epub 2011 Jan 21.

DOI:10.1088/1741-2560/8/1/016011
PMID:21252415
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3056083/
Abstract

Normal brain function requires constant adaptation, as an organism learns to associate important sensory stimuli with the appropriate motor actions. Neurological disorders may disrupt these learned associations and require the nervous system to reorganize itself. As a consequence, neural plasticity is a crucial component of normal brain function and a critical mechanism for recovery from injury. Associative, or Hebbian, pairing of pre- and post-synaptic activity has been shown to alter stimulus-evoked responses in vivo; however, to date, such protocols have not been shown to affect the animal's subsequent behavior. We paired stimulus trains separated by a brief time delay to two electrodes in rat sensorimotor cortex, which changed the statistical pattern of spikes during subsequent behavior. These changes were consistent with strengthened functional connections from the leading electrode to the lagging electrode. We then trained rats to respond to a microstimulation cue, and repeated the paradigm using the cue electrode as the leading electrode. This pairing lowered the rat's ICMS-detection threshold, with the same dependence on intra-electrode time lag that we found for the functional connectivity changes. The timecourse of the behavioral effects was very similar to that of the connectivity changes. We propose that the behavioral changes were a consequence of strengthened functional connections from the cue electrode to other regions of sensorimotor cortex. Such paradigms might be used to augment recovery from a stroke, or to promote adaptation in a bidirectional brain-machine interface.

摘要

正常的大脑功能需要不断的适应,因为生物体学会将重要的感觉刺激与适当的运动动作联系起来。神经紊乱可能会破坏这些已习得的联系,需要神经系统重新组织自身。因此,神经可塑性是正常大脑功能的关键组成部分,也是从损伤中恢复的关键机制。已经表明,前突触和后突触活动的联想性或海伯配对会改变体内刺激诱发的反应;然而,迄今为止,这些方案尚未显示会影响动物随后的行为。我们将刺激训练与短时间延迟配对到大鼠感觉运动皮层的两个电极上,这改变了随后行为期间的尖峰统计模式。这些变化与从领先电极到滞后电极的功能连接增强一致。然后,我们训练大鼠对微刺激线索做出反应,并使用线索电极作为领先电极重复该范式。这种配对降低了大鼠的 ICMS 检测阈值,与我们在功能连接变化中发现的电极内时间延迟的依赖性相同。行为效应的时程与连接变化非常相似。我们提出,行为变化是从线索电极到感觉运动皮层其他区域的功能连接增强的结果。这种范例可能用于增强中风后的恢复,或促进双向脑机接口的适应。

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