Beyond synaptic plasticity: a summary of a linear model of the cerebellar locomotor computation.

IF 2.9 3区 医学 Q2 NEUROSCIENCES
Frontiers in Neural Circuits Pub Date : 2026-05-12 eCollection Date: 2026-01-01 DOI:10.3389/fncir.2026.1815319
Mike Gilbert, Anders Rasmussen
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引用次数: 0

Abstract

We present a summary of ideas that attempt to explain how the locomotor cerebellum may represent and process information. It includes the proposals that (i) the main network computation is a passive and unlearned effect of cell type morphologies and neural architecture; (ii) information has topographically defined spatial dimensions; (iii) it is coded at collective level, at any instant, in any random sample of functionally grouped signals; (iv) topographical organization extends outside the cerebellum and maps to the peripheral nervous system; and (v) learning and memory are at microzone level and in a supplementary role. The aim is to provide competition for traditional learning models and to challenge some common assumptions. We have found that the main resistance to the proposals is in these areas: loyalty to the traditional model; mathematically, the computation is unexpectedly unsophisticated; on the face of it, the mechanism is resource-heavy; we propose that neuroanatomy automates motor coordination and converts feedback into motor output in real time. Some of the ideas are contentious. We argue, nonetheless, that the proposals can explain the evidence.

超越突触可塑性:小脑运动计算的线性模型综述。
我们提出了一个想法的总结,试图解释运动小脑如何代表和处理信息。它包括以下建议:(i)主要网络计算是细胞类型形态和神经结构的被动和非学习效应;信息具有地形上确定的空间维度;(iii)在任何时刻,在功能分组信号的任意随机样本中,在集体水平上进行编码;(iv)地形组织延伸到小脑之外并映射到周围神经系统;(五)学习和记忆处于微区水平,起补充作用。其目的是为传统的学习模式提供竞争,并挑战一些常见的假设。我们发现,对这些建议的主要阻力在于以下几个方面:对传统模式的忠诚;在数学上,计算出乎意料地简单;从表面上看,该机制资源繁重;我们建议神经解剖学自动化运动协调,并将反馈实时转换为运动输出。其中一些观点是有争议的。尽管如此,我们认为这些建议可以解释证据。
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来源期刊
CiteScore
6.00
自引率
5.70%
发文量
135
审稿时长
4-8 weeks
期刊介绍: Frontiers in Neural Circuits publishes rigorously peer-reviewed research on the emergent properties of neural circuits - the elementary modules of the brain. Specialty Chief Editors Takao K. Hensch and Edward Ruthazer at Harvard University and McGill University respectively, are supported by an outstanding Editorial Board of international experts. This multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics and the public worldwide. Frontiers in Neural Circuits launched in 2011 with great success and remains a "central watering hole" for research in neural circuits, serving the community worldwide to share data, ideas and inspiration. Articles revealing the anatomy, physiology, development or function of any neural circuitry in any species (from sponges to humans) are welcome. Our common thread seeks the computational strategies used by different circuits to link their structure with function (perceptual, motor, or internal), the general rules by which they operate, and how their particular designs lead to the emergence of complex properties and behaviors. Submissions focused on synaptic, cellular and connectivity principles in neural microcircuits using multidisciplinary approaches, especially newer molecular, developmental and genetic tools, are encouraged. Studies with an evolutionary perspective to better understand how circuit design and capabilities evolved to produce progressively more complex properties and behaviors are especially welcome. The journal is further interested in research revealing how plasticity shapes the structural and functional architecture of neural circuits.
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