Neural Mechanisms Underlying Functional Plasticity of the Human Brain

人脑功能可塑性背后的神经机制

基本信息

  • 批准号:
    RGPIN-2016-05343
  • 负责人:
  • 金额:
    $ 1.82万
  • 依托单位:
  • 依托单位国家:
    加拿大
  • 项目类别:
    Discovery Grants Program - Individual
  • 财政年份:
    2020
  • 资助国家:
    加拿大
  • 起止时间:
    2020-01-01 至 2021-12-31
  • 项目状态:
    已结题

项目摘要

Learning and skill acquisition rely to a large extent on implicit processes that occur independent of conscious awareness, both on short and long timescales. An example on a short timescale is repetition priming (RP) improved performance in identifying, producing, or classifying a stimulus upon repetition of the same or a related stimulus. Neuroimaging reveals that RP is often accompanied by repetition suppression (RS) reduced neural activation in parts of the brain that are critical for the task at hand. Despite 20 years of research, the link between RP and RS remains elusive. Many theories have focused on changes in local activity within discrete brain regions. However, an alternative explanation is that RS might be a consequence of more efficient communication across large-scale cortical networks. By this account, repetition leads to more efficient coupling across brain regions (functional connectivity: FC), which simultaneously reduces local neural activity and enhances cognitive performance. However, there is little direct evidence to support this hypothesis to date. Thus, there is a critical need for studies that directly test this hypothesis to elucidate the neural mechanism underlying this fundamental process. Regarding longer timescales, evidence demonstrates that spontaneous fluctuations of brain activity across large-scale networks play a fundamental role in learning and skill acquisition as well. While these patterns of activity persist, largely independent of ongoing thoughts, they are also modulated by experienc to some extent, and this modulation has an impact on future behaviour and performance. Little is known about how this intrinsic activity interacts with RP or RS, but this could be a fundamental mechanism underlying long-term functional plasticity in the brain; thus, there is a critical need for studies that elucidate the relationship between repeated experiences, patterns of intrinsic activity, and long-term behavioural facilitation. This research proposal has 2 primary objectives: 1) To determine if RP and RS reflect neural efficiency due to enhanced FC, and if they interact with long-term neurocognitive plasticity reflected by intrinsic activity, using fMRI. 2) To establish causal cortico-cortical and brain-behaviour relationships that lead to both short- and long-term neurocognitive plasticity by experimentally modulating brain activity using transcranial magnetic stimulation. The long-term objective is to develop a comprehensive model that characterizes and quantifies the causal interrelationships between implicit processes acting on different timescales, to understand how neurocognitive plasticity shapes cognitive performance over time. This work will produce critically needed insight into these fundamental processes, of which we currently know little, and will have a significant impact on the fields of human learning and cognition.
学习和技能获取在很大程度上依赖于独立于意识意识而发生的内隐过程,无论是短期还是长期。短时间尺度上的一个例子是重复启动(RP)在重复相同或相关刺激时提高了识别、产生或分类刺激的性能。神经影像学显示,RP 通常伴随着重复抑制 (RS),从而减少了大脑中对当前任务至关重要的部分的神经激活。尽管经过 20 年的研究,RP 和 RS 之间的联系仍然难以捉摸。许多理论都关注离散大脑区域内局部活动的变化。然而,另一种解释是,RS 可能是大规模皮层网络更有效通信的结果。由此看来,重复会导致大脑区域之间更有效的耦合(功能连接:FC),同时减少局部神经活动并增强认知能力。然而,迄今为止,几乎没有直接证据支持这一假设。因此,迫切需要直接检验这一假设的研究,以阐明这一基本过程背后的神经机制。对于更长的时间尺度,有证据表明,大规模网络中大脑活动的自发波动在学习和技能获取中也发挥着重要作用。虽然这些活动模式持续存在,很大程度上独立于正在进行的想法,但它们也在某种程度上受到经验的调节,并且这种调节对未来的行为和表现有影响。人们对这种内在活动如何与 RP 或 RS 相互作用知之甚少,但这可能是大脑长期功能可塑性的基本机制。因此,迫切需要进行研究来阐明重复经历、内在活动模式和长期行为促进之间的关系。该研究计划有两个主要目标: 1) 使用 fMRI 确定 RP 和 RS 是否反映了 FC 增强带来的神经效率,以及它们是否与内在活动反映的长期神经认知可塑性相互作用。 2)通过使用经颅磁刺激实验调节大脑活动,建立因果皮质-皮质和大脑-行为关系,从而导致短期和长期神经认知可塑性。 长期目标是开发一个综合模型,描述和量化作用于不同时间尺度的隐性过程之间的因果关系,以了解神经认知可塑性如何随着时间的推移塑造认知表现。这项工作将对这些我们目前知之甚少的基本过程产生急需的洞察力,并将对人类学习和认知领域产生重大影响。

项目成果

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Stevens, William其他文献

Effects of aspirin on dementia and cognitive function in diabetic patients: the ASCEND trial.
  • DOI:
    10.1093/eurheartj/ehac179
  • 发表时间:
    2022-06-01
  • 期刊:
  • 影响因子:
    39.3
  • 作者:
    Parish, Sarah;Mafham, Marion;Offer, Alison;Barton, Jill;Wallendszus, Karl;Stevens, William;Buck, Georgina;Haynes, Richard;Collins, Rory;Bowman, Louise;Armitage, Jane
  • 通讯作者:
    Armitage, Jane

Stevens, William的其他文献

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{{ truncateString('Stevens, William', 18)}}的其他基金

Enhanced Neuroimaging Infrastructure for Innovative Visual Neuroscience
增强创新视觉神经科学的神经影像基础设施
  • 批准号:
    RTI-2023-00465
  • 财政年份:
    2022
  • 资助金额:
    $ 1.82万
  • 项目类别:
    Research Tools and Instruments
Neural Mechanisms Underlying Functional Plasticity of the Human Brain
人脑功能可塑性背后的神经机制
  • 批准号:
    RGPIN-2016-05343
  • 财政年份:
    2022
  • 资助金额:
    $ 1.82万
  • 项目类别:
    Discovery Grants Program - Individual
Neural Mechanisms Underlying Functional Plasticity of the Human Brain
人脑功能可塑性背后的神经机制
  • 批准号:
    RGPIN-2016-05343
  • 财政年份:
    2021
  • 资助金额:
    $ 1.82万
  • 项目类别:
    Discovery Grants Program - Individual
Neural Mechanisms Underlying Functional Plasticity of the Human Brain
人脑功能可塑性背后的神经机制
  • 批准号:
    RGPIN-2016-05343
  • 财政年份:
    2019
  • 资助金额:
    $ 1.82万
  • 项目类别:
    Discovery Grants Program - Individual
Neural Mechanisms Underlying Functional Plasticity of the Human Brain
人脑功能可塑性背后的神经机制
  • 批准号:
    RGPIN-2016-05343
  • 财政年份:
    2018
  • 资助金额:
    $ 1.82万
  • 项目类别:
    Discovery Grants Program - Individual
Neural Mechanisms Underlying Functional Plasticity of the Human Brain
人脑功能可塑性背后的神经机制
  • 批准号:
    RGPIN-2016-05343
  • 财政年份:
    2017
  • 资助金额:
    $ 1.82万
  • 项目类别:
    Discovery Grants Program - Individual
Neural Mechanisms Underlying Functional Plasticity of the Human Brain
人脑功能可塑性背后的神经机制
  • 批准号:
    RGPIN-2016-05343
  • 财政年份:
    2016
  • 资助金额:
    $ 1.82万
  • 项目类别:
    Discovery Grants Program - Individual

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