Active motor preparation drives corticospinal facilitation during interception planning.

IF 2.3 3区 医学 Q3 NEUROSCIENCES
Journal of neurophysiology Pub Date : 2026-09-01 Epub Date: 2026-08-19 DOI:10.1152/jn.00017.2026
Justin R McCurdy, Brendan Jarvis, Emma Whitman, Krithi Ariga, Asher Khan, Deborah A Barany
{"title":"Active motor preparation drives corticospinal facilitation during interception planning.","authors":"Justin R McCurdy, Brendan Jarvis, Emma Whitman, Krithi Ariga, Asher Khan, Deborah A Barany","doi":"10.1152/jn.00017.2026","DOIUrl":null,"url":null,"abstract":"<p><p>Intercepting a moving target requires integrating visual motion information with motor preparation, yet how active motor preparation and gaze strategy jointly shape corticospinal excitability during interception planning remains unclear. We applied single-pulse transcranial magnetic stimulation over primary motor cortex to probe corticospinal excitability while participants either prepared to intercept a moving target or passively viewed its motion. Targets moved at one of two speeds, and participants judged target speed relative to a reference after each trial. Across blocks, participants were instructed to either smoothly pursue the target or fixate their eyes on the interception zone. Motor-evoked potentials were elicited at baseline, after task instruction, early during target motion, or shortly before target arrival. Task and gaze strategy interacted to influence both perceptual judgments and corticospinal excitability. Preparing to intercept produced a robust facilitation of corticospinal excitability immediately before movement onset, regardless of gaze strategy. In contrast, corticospinal excitability during passive viewing did not differ from baseline. Smooth pursuit improved perceptual accuracy and reduced interception timing error compared with fixation but did not independently influence corticospinal facilitation. These findings demonstrate that active motor preparation is the primary determinant of the transition to a state of facilitated excitability during interception planning, whereas eye movements modulate perceptual estimates and support behavioral performance.<b>NEW & NOTEWORTHY</b> This study dissociates the contributions of visual tracking, eye movements, and active motor preparation to corticospinal excitability during interception. Here, we show that corticospinal facilitation emerges primarily when an action is planned, whereas passive viewing remains at baseline despite identical visual input. Smooth pursuit enhanced perceptual accuracy and interception timing but had a limited effect on corticospinal excitability, highlighting active motor preparation as the key driver of corticospinal output.</p>","PeriodicalId":16563,"journal":{"name":"Journal of neurophysiology","volume":" ","pages":"1098-1109"},"PeriodicalIF":2.3000,"publicationDate":"2026-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of neurophysiology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1152/jn.00017.2026","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/8/19 0:00:00","PubModel":"Epub","JCR":"Q3","JCRName":"NEUROSCIENCES","Score":null,"Total":0}
引用次数: 0

Abstract

Intercepting a moving target requires integrating visual motion information with motor preparation, yet how active motor preparation and gaze strategy jointly shape corticospinal excitability during interception planning remains unclear. We applied single-pulse transcranial magnetic stimulation over primary motor cortex to probe corticospinal excitability while participants either prepared to intercept a moving target or passively viewed its motion. Targets moved at one of two speeds, and participants judged target speed relative to a reference after each trial. Across blocks, participants were instructed to either smoothly pursue the target or fixate their eyes on the interception zone. Motor-evoked potentials were elicited at baseline, after task instruction, early during target motion, or shortly before target arrival. Task and gaze strategy interacted to influence both perceptual judgments and corticospinal excitability. Preparing to intercept produced a robust facilitation of corticospinal excitability immediately before movement onset, regardless of gaze strategy. In contrast, corticospinal excitability during passive viewing did not differ from baseline. Smooth pursuit improved perceptual accuracy and reduced interception timing error compared with fixation but did not independently influence corticospinal facilitation. These findings demonstrate that active motor preparation is the primary determinant of the transition to a state of facilitated excitability during interception planning, whereas eye movements modulate perceptual estimates and support behavioral performance.NEW & NOTEWORTHY This study dissociates the contributions of visual tracking, eye movements, and active motor preparation to corticospinal excitability during interception. Here, we show that corticospinal facilitation emerges primarily when an action is planned, whereas passive viewing remains at baseline despite identical visual input. Smooth pursuit enhanced perceptual accuracy and interception timing but had a limited effect on corticospinal excitability, highlighting active motor preparation as the key driver of corticospinal output.

在截击计划期间,主动运动准备驱动皮质脊髓促进。
拦截移动目标需要将视觉运动信息与运动准备相结合,但在拦截计划期间,主动运动准备和凝视策略如何共同塑造皮质脊髓兴奋性尚不清楚。当参与者准备拦截移动目标或被动观看其运动时,我们在初级运动皮层上应用单脉冲经颅磁刺激来探测皮质脊髓的兴奋性。目标以两种速度中的一种移动,参与者在每次试验后判断目标相对于参考的速度。在各个街区,参与者被指示要么平稳地追逐目标,要么把眼睛盯在拦截区。运动诱发电位在基线、任务指示后、目标运动早期或目标到达前不久被激发。任务和凝视策略相互作用影响知觉判断和皮质脊髓兴奋性。无论凝视策略如何,在运动开始之前,准备拦截会产生强大的皮质脊髓兴奋性促进。相比之下,被动观看期间的皮质脊髓兴奋性与基线没有差异。与固定相比,平滑追踪提高了知觉准确性,减少了拦截时间误差,但不独立影响皮质脊髓促进。这些发现表明,在拦截计划期间,主动运动准备是过渡到易兴奋状态的主要决定因素,而眼动调节知觉估计并支持行为表现。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Journal of neurophysiology
Journal of neurophysiology 医学-神经科学
CiteScore
4.80
自引率
8.00%
发文量
255
审稿时长
2-3 weeks
期刊介绍: The Journal of Neurophysiology publishes original articles on the function of the nervous system. All levels of function are included, from the membrane and cell to systems and behavior. Experimental approaches include molecular neurobiology, cell culture and slice preparations, membrane physiology, developmental neurobiology, functional neuroanatomy, neurochemistry, neuropharmacology, systems electrophysiology, imaging and mapping techniques, and behavioral analysis. Experimental preparations may be invertebrate or vertebrate species, including humans. Theoretical studies are acceptable if they are tied closely to the interpretation of experimental data and elucidate principles of broad interest.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信
小红书