皮质脊髓-运动神经元配对刺激增强老年人弹道运动学习和皮质脊髓可塑性。

IF 4.7 2区 医学 Q1 NEUROSCIENCES
Jonas Rud Bjørndal, Lasse Jespersen, Mikkel Malling Beck, Anke Ninija Karabanov, Lasse Christiansen, Jesper Lundbye-Jensen
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引用次数: 0

摘要

成年后期伴随着体力运动能力的下降和神经可塑性的降低,这可能会影响运动练习和学习的效果。皮质神经元(CM)连接可以通过个体化配对皮质脊髓-运动神经元刺激(PCMS)非侵入性地靶向,以启动年轻人的弹道运动学习。然而,PCMS对老年人运动输出和弹道运动学习的启动效应尚不清楚。本研究的第一部分调查了年轻人(20-30岁)和老年人(65-75岁)的弹道运动表现和学习,研究了1周后快速食指屈曲和延迟保持的峰值加速度的变化。结果表明,与年轻人相比,老年人表现出更低的最大加速度和更小的练习进步,表明较差的学习和低水平的延迟记忆。本研究的第二部分探讨了PCMS对老年人运动学习和皮质脊髓兴奋性的影响。在整个实验过程中,通过记录第一背骨间的运动诱发电位来评估皮质脊髓兴奋性。与SHAM相比,PCMS增加了练习后的弹道学习和皮质脊髓兴奋性。重要的是,联合PCMS和运动训练也增强了长期记忆,7天后的表现仍然增强。这意味着PCMS有效地恢复了老年人原本缺失的长期学习。我们证明,PCMS启动伴随运动学习的经验依赖的可塑性,从而对老年人的运动表现产生长期的好处。这些发现强调了PCMS在增强老年人运动练习和功能能力方面的潜力。重点:成年后期与剧烈运动时脊髓运动神经元的激活减少有关,导致运动变慢和不精确。与年轻人(20-30岁)相比,老年人(65-75岁)的弹道运动表现较低;此外,老年人在练习中表现出较小的进步,记忆力也较差。单次皮质脊髓-运动神经元配对刺激(PCMS)增加皮质脊髓兴奋性,并启动老年人的弹道运动学习。单次PCMS可提高弹道运动学习后的长期记忆。我们提供了原理证明,PCMS代表了一种潜在的策略,可以增强运动练习的效果,并抵消与年龄相关的运动功能下降。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Paired corticospinal-motoneuronal stimulation enhances ballistic motor learning and corticospinal plasticity in older adults.

Late adulthood is accompanied by declines in manual motor performance and reduced neuroplasticity, which can influence the effects of motor practice and learning. Corticomotoneuronal (CM) connectivity can be targeted non-invasively through individualized paired corticospinal-motoneuronal stimulation (PCMS) to prime ballistic motor learning in young adults. However, the priming effects of PCMS on motor output and ballistic motor learning in older adults remain unexplored. Part one of this study investigates ballistic motor performance and learning in young (20-30 years) and older (65-75 years) adults as within-session changes in peak acceleration of rapid index finger flexions and delayed retention 1 week later. The results demonstrate that older adults display lower maximal acceleration compared to young adults and smaller improvements with practice, indicating inferior learning and low levels of delayed retention. Part two of the study investigates the effects of PCMS on motor learning and corticospinal excitability in older adults. Corticospinal excitability was assessed throughout the experiment by recording motor evoked potentials from the first dorsal interosseous. PCMS increased subsequent ballistic learning and corticospinal excitability after practice compared to SHAM. Importantly, combined PCMS and motor practice also enhanced long-term retention, and performance remained enhanced 7 days later. This means that PCMS effectively reinstated the otherwise absent long-term learning in older adults. We demonstrate that PCMS primes experience-dependent plasticity accompanying motor learning resulting in long-term benefits on motor performance in older adults. These findings highlight the potential of PCMS to enhance the effects of motor practice and benefit functional abilities in older adults. KEY POINTS: Late adulthood is associated with reduced activation of spinal motoneurons during vigorous movements, resulting in slower and less precise movements. Older adults (aged 65-75 years) display lower ballistic motor performance compared to younger adults (aged 20-30 years); furthermore, older adults exhibit smaller improvements during practice, and lower retention. A single session of paired corticospinal-motoneuronal stimulation (PCMS) increases corticospinal excitability and primes within-session ballistic motor learning in older adults. A single session of PCMS improves long-term retention following ballistic motor learning. We provide proof-of-principle that PCMS represents a potential strategy to enhance the effects of motor practice and counteract age-related decline in motor function.

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来源期刊
Journal of Physiology-London
Journal of Physiology-London 医学-神经科学
CiteScore
9.70
自引率
7.30%
发文量
817
审稿时长
2 months
期刊介绍: The Journal of Physiology publishes full-length original Research Papers and Techniques for Physiology, which are short papers aimed at disseminating new techniques for physiological research. Articles solicited by the Editorial Board include Perspectives, Symposium Reports and Topical Reviews, which highlight areas of special physiological interest. CrossTalk articles are short editorial-style invited articles framing a debate between experts in the field on controversial topics. Letters to the Editor and Journal Club articles are also published. All categories of papers are subjected to peer reivew. The Journal of Physiology welcomes submitted research papers in all areas of physiology. Authors should present original work that illustrates new physiological principles or mechanisms. Papers on work at the molecular level, at the level of the cell membrane, single cells, tissues or organs and on systems physiology are all acceptable. Theoretical papers and papers that use computational models to further our understanding of physiological processes will be considered if based on experimentally derived data and if the hypothesis advanced is directly amenable to experimental testing. While emphasis is on human and mammalian physiology, work on lower vertebrate or invertebrate preparations may be suitable if it furthers the understanding of the functioning of other organisms including mammals.
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