Transformation of neural coding for vibrotactile stimuli along the ascending somatosensory pathway.

IF 14.7 1区 医学 Q1 NEUROSCIENCES Neuron Pub Date : 2024-10-09 Epub Date: 2024-08-06 DOI:10.1016/j.neuron.2024.07.005
Kuo-Sheng Lee, Alastair J Loutit, Dominica de Thomas Wagner, Mark Sanders, Mario Prsa, Daniel Huber
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Abstract

In mammals, action potentials fired by rapidly adapting mechanosensitive afferents are known to reliably time lock to the cycles of a vibration. How and where along the ascending neuraxis is the peripheral afferent temporal code transformed into a rate code are currently not clear. Here, we probed the encoding of vibrotactile stimuli with electrophysiological recordings along major stages of the ascending somatosensory pathway in mice. We discovered the main transformation step was identified at the level of the thalamus, and parvalbumin-positive interneurons in thalamic reticular nucleus participate in sharpening frequency selectivity and in disrupting the precise spike timing. When frequency-specific microstimulation was applied within the brainstem, it generated frequency selectivity reminiscent of real vibration responses in the somatosensory cortex and could provide informative and robust signals for learning in behaving mice. Taken together, these findings could guide biomimetic stimulus strategies to activate specific nuclei along the ascending somatosensory pathway for neural prostheses.

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振动触觉刺激神经编码沿着体感上升通路的转变。
在哺乳动物中,由快速适应的机械敏感传入神经发射的动作电位能够可靠地锁定振动周期的时间。目前尚不清楚外周传入的时间编码如何以及在哪条神经轴上被转化为速率编码。在这里,我们通过对小鼠体感上升通路主要阶段的电生理记录,探究了振动触觉刺激的编码。我们发现,主要的转换步骤是在丘脑水平上确定的,丘脑网状核中的副发光素阳性中间神经元参与了频率选择性的锐化,并破坏了精确的尖峰计时。当频率特异性微刺激应用于脑干时,它所产生的频率选择性让人联想到体感皮层中的真实振动反应,并能为行为小鼠的学习提供信息和稳健的信号。综上所述,这些发现可以指导生物仿真刺激策略,激活神经假体升序躯体感觉通路上的特定神经核。
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来源期刊
Neuron
Neuron 医学-神经科学
CiteScore
24.50
自引率
3.10%
发文量
382
审稿时长
1 months
期刊介绍: Established as a highly influential journal in neuroscience, Neuron is widely relied upon in the field. The editors adopt interdisciplinary strategies, integrating biophysical, cellular, developmental, and molecular approaches alongside a systems approach to sensory, motor, and higher-order cognitive functions. Serving as a premier intellectual forum, Neuron holds a prominent position in the entire neuroscience community.
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