体感丘脑触觉加工的皮质丘脑调节。

IF 4.7 2区 医学 Q1 NEUROSCIENCES
Avisar Einav, Rony Azouz
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引用次数: 0

摘要

大脑对感觉信息的处理涉及前馈和反馈途径之间复杂的相互作用,包括皮质丘脑反馈。虽然从皮层第6层到感觉丘脑的反馈是已知的调节感觉信号,但其确切的功能仍然是难以捉摸的。本研究利用轻麻醉大鼠体内电生理记录,探讨第6层反馈对腹侧后内侧核感觉传递的影响。通过在丘脑记录过程中局部给药,我们研究了丘脑皮质神经元如何影响触觉刺激转化为神经元放电特征。我们的研究结果表明,在低刺激强度下,增加皮质动力可以增强丘脑的反应强度,但在高刺激强度下会降低丘脑的反应强度,而减少皮质动力则会产生相反的效果。此外,我们观察到皮层对丘脑神经元的双向影响延伸到刺激大小依赖的感觉适应和第6层动力学的爆发倾向调节。具体来说,在低刺激强度下,皮质动力增强会降低丘脑的感觉适应性,增加突发倾向,在高刺激强度下没有观察到变化,而皮质动力减弱则会产生相反的效果。我们发现丘脑神经元可以区分刺激,皮层的影响随刺激强度的变化而变化。增强的皮质动力在低强度下增强辨别,而减弱的动力则有相反的效果。我们的研究结果表明,皮层对腹侧后内侧核触觉转换的控制不是二进制开关,而是一个动态调制器,根据皮层动态实时调节丘脑转换。这种机制可以很好地调节感官处理以满足环境和行为的需求。重点:该研究通过检查大脑区域之间的相互作用来研究大脑中的触摸处理。具体来说,我们研究皮层第6层如何影响丘脑的感觉信号处理。我们用药物控制第六层的活动,观察丘脑触觉反应的变化。皮层活动的增加增强了弱触摸信号,但抑制了丘脑中的强触摸信号;较低的活动则产生相反的效果。在低刺激强度下,增加的皮质动力学降低了丘脑的感觉适应性,增加了爆发倾向,而在高刺激强度下没有变化。研究表明,大脑对处理感官信息的控制不仅仅是一个开/关开关,而是一个动态系统,可以根据不同的情况进行实时调整。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Corticothalamic modulation of somatosensory thalamic tactile processing

Corticothalamic modulation of somatosensory thalamic tactile processing
The brain's processing of sensory information involves intricate interactions between feedforward and feedback pathways, including corticothalamic feedback. Although feedback from cortical Layer 6 to the sensory thalamus is known to regulate sensory signalling, its precise function remains elusive. This study delves into the impact of Layer 6 feedback on sensory transmission in the ventral posteromedial nucleus using in vivo electrophysiology recordings in lightly anesthetized rats. By local administration of drugs to the barrel cortex during thalamic recordings, we investigate how corticothalamic neurons influence the transformation of tactile stimuli into neuronal discharge characteristics. Our findings reveal that increasing cortical dynamics enhances thalamic response magnitude at low stimulus intensities but decreases it at high intensities, whereas reducing cortical dynamics produces the opposite effect. Moreover, we observe bidirectional cortical influence on thalamic neurons extending to stimulus magnitude-dependent sensory adaptation and burst propensity modulation by Layer 6 dynamics. Specifically, increased cortical dynamics reduce thalamic sensory adaptation and increase burst propensity at low stimulus intensities, with no observed change at high intensities, whereas decreased cortical dynamics elicit opposite effects. We show that thalamic neurons can discriminate between stimuli, with cortical influence varying by stimulus intensity. Increased cortical dynamics enhances discrimination at low intensities, whereas reduced dynamics has the opposite effect. Our findings suggest that cortical control of ventral posteromedial nucleus tactile transformation is not a binary switch but a dynamic modulator, adjusting thalamic transformations in real time based on cortical dynamics. This mechanism finely tunes sensory processing to meet environmental and behavioural demands.

Key points

  • The study investigates touch processing in the brain by examining interactions between brain regions. Specifically, we study how cortical Layer 6 influences sensory signal processing in the thalamus.
  • We manipulated Layer 6 activity with drugs and observed resulting changes in thalamic touch responses.
  • Increased cortical activity enhanced weak touch signals but dampened strong ones in the thalamus; lower activity had the opposite effect.
  • Increased cortical dynamics reduced thalamic sensory adaptation and increased burst propensity at low stimulus intensities, with no change at high intensities.
  • The study shows that the brain's control over how it processes sensory information is not just an on/off switch but a dynamic system that adjusts in real time to different situations.
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来源期刊
Journal of Physiology-London
Journal of Physiology-London 医学-神经科学
CiteScore
9.70
自引率
7.30%
发文量
817
审稿时长
2 months
期刊介绍: The Journal of Physiology publishes full-length original Research Papers and Techniques for Physiology, which are short papers aimed at disseminating new techniques for physiological research. Articles solicited by the Editorial Board include Perspectives, Symposium Reports and Topical Reviews, which highlight areas of special physiological interest. CrossTalk articles are short editorial-style invited articles framing a debate between experts in the field on controversial topics. Letters to the Editor and Journal Club articles are also published. All categories of papers are subjected to peer reivew. The Journal of Physiology welcomes submitted research papers in all areas of physiology. Authors should present original work that illustrates new physiological principles or mechanisms. Papers on work at the molecular level, at the level of the cell membrane, single cells, tissues or organs and on systems physiology are all acceptable. Theoretical papers and papers that use computational models to further our understanding of physiological processes will be considered if based on experimentally derived data and if the hypothesis advanced is directly amenable to experimental testing. While emphasis is on human and mammalian physiology, work on lower vertebrate or invertebrate preparations may be suitable if it furthers the understanding of the functioning of other organisms including mammals.
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