在运动敏感神经元的多层网络中,尖峰时间依赖性可塑性部分补偿了神经延迟。

IF 4.3 2区 生物学
PLoS Computational Biology Pub Date : 2023-09-06 eCollection Date: 2023-09-01 DOI:10.1371/journal.pcbi.1011457
Charlie M Sexton, Anthony N Burkitt, Hinze Hogendoorn
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引用次数: 1

摘要

大脑实时表示外部世界的能力受到神经处理需要时间这一事实的影响。由于神经延迟随着信息在视觉系统中的传播而积累,因此在每个层次级别编码的表示都基于相对于外部世界逐渐过时的输入。这种“表征滞后”与定位移动物体的任务特别相关,因为物体的位置随着时间的变化而变化,其位置的神经表征可能滞后于其真实位置。汇聚的证据表明,大脑已经进化出了机制,可以通过推断运动物体沿其轨迹的位置来补偿其固有的延迟。我们之前已经展示了尖峰时间依赖性可塑性(STDP)如何通过将第二层神经元的感受野向移动刺激的相反方向移动,在速度调谐神经元的两层前馈网络中实现运动外推。目前的研究扩展了这项工作,对网络进行了两项重要的更改,使其更符合生物学:我们将网络扩展到多层,以反映视觉层次的深度,并实现了更逼真的突触时间过程。我们研究了STDP驱动的感受野在几个层面上的偏移的积累,观察到表征滞后的速度依赖性减少。这些结果突出了STDP作为延迟补偿的发展策略的作用,STDP纯粹沿着前馈路径运行。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Spike-timing dependent plasticity partially compensates for neural delays in a multi-layered network of motion-sensitive neurons.

Spike-timing dependent plasticity partially compensates for neural delays in a multi-layered network of motion-sensitive neurons.

Spike-timing dependent plasticity partially compensates for neural delays in a multi-layered network of motion-sensitive neurons.

Spike-timing dependent plasticity partially compensates for neural delays in a multi-layered network of motion-sensitive neurons.

The ability of the brain to represent the external world in real-time is impacted by the fact that neural processing takes time. Because neural delays accumulate as information progresses through the visual system, representations encoded at each hierarchical level are based upon input that is progressively outdated with respect to the external world. This 'representational lag' is particularly relevant to the task of localizing a moving object-because the object's location changes with time, neural representations of its location potentially lag behind its true location. Converging evidence suggests that the brain has evolved mechanisms that allow it to compensate for its inherent delays by extrapolating the position of moving objects along their trajectory. We have previously shown how spike-timing dependent plasticity (STDP) can achieve motion extrapolation in a two-layer, feedforward network of velocity-tuned neurons, by shifting the receptive fields of second layer neurons in the opposite direction to a moving stimulus. The current study extends this work by implementing two important changes to the network to bring it more into line with biology: we expanded the network to multiple layers to reflect the depth of the visual hierarchy, and we implemented more realistic synaptic time-courses. We investigate the accumulation of STDP-driven receptive field shifts across several layers, observing a velocity-dependent reduction in representational lag. These results highlight the role of STDP, operating purely along the feedforward pathway, as a developmental strategy for delay compensation.

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来源期刊
PLoS Computational Biology
PLoS Computational Biology 生物-生化研究方法
CiteScore
7.10
自引率
4.70%
发文量
820
期刊介绍: PLOS Computational Biology features works of exceptional significance that further our understanding of living systems at all scales—from molecules and cells, to patient populations and ecosystems—through the application of computational methods. Readers include life and computational scientists, who can take the important findings presented here to the next level of discovery. Research articles must be declared as belonging to a relevant section. More information about the sections can be found in the submission guidelines. Research articles should model aspects of biological systems, demonstrate both methodological and scientific novelty, and provide profound new biological insights. Generally, reliability and significance of biological discovery through computation should be validated and enriched by experimental studies. Inclusion of experimental validation is not required for publication, but should be referenced where possible. Inclusion of experimental validation of a modest biological discovery through computation does not render a manuscript suitable for PLOS Computational Biology. Research articles specifically designated as Methods papers should describe outstanding methods of exceptional importance that have been shown, or have the promise to provide new biological insights. The method must already be widely adopted, or have the promise of wide adoption by a broad community of users. Enhancements to existing published methods will only be considered if those enhancements bring exceptional new capabilities.
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