Distinct patterns of connectivity with the motor cortex reflect different components of sensorimotor learning.

IF 9.8 1区 生物学 Q1 Agricultural and Biological Sciences PLoS Biology Pub Date : 2024-12-03 eCollection Date: 2024-12-01 DOI:10.1371/journal.pbio.3002934
Corson N Areshenkoff, Anouk J de Brouwer, Daniel J Gale, Joseph Y Nashed, Jonathan Smallwood, J Randall Flanagan, Jason P Gallivan
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Abstract

Sensorimotor learning is supported by multiple competing processes that operate concurrently, making it a challenge to elucidate their neural underpinnings. Here, using human functional MRI, we identify 3 distinct axes of connectivity between the motor cortex and other brain regions during sensorimotor adaptation. These 3 axes uniquely correspond to subjects' degree of implicit learning, performance errors and explicit strategy use, and involve different brain networks situated at increasing levels of the cortical hierarchy. We test the generalizability of these neural axes to a separate form of motor learning known to rely mainly on explicit processes and show that it is only the Explicit neural axis, composed of higher-order areas in transmodal cortex, that predicts learning in this task. Together, our study uncovers multiple distinct patterns of functional connectivity with motor cortex during sensorimotor adaptation, the component processes that these patterns support, and how they generalize to other forms of motor learning.

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与运动皮层的不同连接模式反映了感觉运动学习的不同组成部分。
感觉运动学习是由多个相互竞争的过程同时运作的,这使得阐明它们的神经基础成为一个挑战。在这里,使用人类功能MRI,我们确定了在感觉运动适应过程中运动皮层和其他大脑区域之间的3个不同的连接轴。这三个轴分别对应于被试的内隐学习、表现错误和外显策略使用的程度,并涉及位于皮层层次增加水平的不同大脑网络。我们测试了这些神经轴对一种独立形式的运动学习的普遍性,这种运动学习主要依赖于外显过程,并表明只有由跨模态皮层的高阶区域组成的外显神经轴才能预测这项任务中的学习。总之,我们的研究揭示了在感觉运动适应过程中与运动皮层的功能连接的多种不同模式,这些模式支持的组成过程,以及它们如何推广到其他形式的运动学习。
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来源期刊
PLoS Biology
PLoS Biology BIOCHEMISTRY & MOLECULAR BIOLOGY-BIOLOGY
CiteScore
15.40
自引率
2.00%
发文量
359
审稿时长
3-8 weeks
期刊介绍: PLOS Biology is the flagship journal of the Public Library of Science (PLOS) and focuses on publishing groundbreaking and relevant research in all areas of biological science. The journal features works at various scales, ranging from molecules to ecosystems, and also encourages interdisciplinary studies. PLOS Biology publishes articles that demonstrate exceptional significance, originality, and relevance, with a high standard of scientific rigor in methodology, reporting, and conclusions. The journal aims to advance science and serve the research community by transforming research communication to align with the research process. It offers evolving article types and policies that empower authors to share the complete story behind their scientific findings with a diverse global audience of researchers, educators, policymakers, patient advocacy groups, and the general public. PLOS Biology, along with other PLOS journals, is widely indexed by major services such as Crossref, Dimensions, DOAJ, Google Scholar, PubMed, PubMed Central, Scopus, and Web of Science. Additionally, PLOS Biology is indexed by various other services including AGRICOLA, Biological Abstracts, BIOSYS Previews, CABI CAB Abstracts, CABI Global Health, CAPES, CAS, CNKI, Embase, Journal Guide, MEDLINE, and Zoological Record, ensuring that the research content is easily accessible and discoverable by a wide range of audiences.
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