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本文引用的文献

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Structural and functional bases for individual differences in motor learning.个体运动学习差异的结构和功能基础。
Hum Brain Mapp. 2011 Mar;32(3):494-508. doi: 10.1002/hbm.21037.
2
Rapid-onset central motor plasticity in multiple sclerosis.多发性硬化症中的快速发作中枢运动可塑性。
Neurology. 2010 Mar 2;74(9):728-35. doi: 10.1212/WNL.0b013e3181d31dcf.
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Trial-to-trial variability of single cells in motor cortices is dynamically modified during visuomotor adaptation.在视觉运动适应过程中,运动皮层单个细胞的逐次试验变异性会被动态改变。
J Neurosci. 2009 Dec 2;29(48):15053-62. doi: 10.1523/JNEUROSCI.3011-09.2009.
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Dynamics of motor-related functional integration during motor sequence learning.运动序列学习过程中运动相关功能整合的动力学。
Neuroimage. 2010 Jan 1;49(1):759-66. doi: 10.1016/j.neuroimage.2009.08.048. Epub 2009 Aug 28.
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Neural substrates of practice structure that support future off-line learning.支持未来离线学习的实践结构的神经基础。
J Neurophysiol. 2009 Oct;102(4):2462-76. doi: 10.1152/jn.00315.2009. Epub 2009 Aug 19.
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What does a structured review of the effectiveness of exercise interventions for persons with multiple sclerosis tell us about the challenges of designing trials?对针对多发性硬化症患者的运动干预效果进行的结构化综述能让我们了解到设计试验存在哪些挑战?
Mult Scler. 2009 Apr;15(4):412-21. doi: 10.1177/1352458508101877.
7
Learning of a sequential motor skill comprises explicit and implicit components that consolidate differently.学习连续性运动技能包括明确和隐性两个不同巩固方式的组成部分。
J Neurophysiol. 2009 May;101(5):2218-29. doi: 10.1152/jn.01138.2007. Epub 2008 Dec 10.
8
Abnormal connectivity of the sensorimotor network in patients with MS: a multicenter fMRI study.多发性硬化症患者感觉运动网络的异常连接:一项多中心功能磁共振成像研究。
Hum Brain Mapp. 2009 Aug;30(8):2412-25. doi: 10.1002/hbm.20679.
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Remyelination in the CNS: from biology to therapy.中枢神经系统中的髓鞘再生:从生物学到治疗
Nat Rev Neurosci. 2008 Nov;9(11):839-55. doi: 10.1038/nrn2480.
10
Structural connectivity influences brain activation during PVSAT in Multiple Sclerosis.在多发性硬化症中,结构连接性会影响静息态动脉自旋标记灌注期间的脑激活。
Neuroimage. 2009 Jan 1;44(1):9-15. doi: 10.1016/j.neuroimage.2008.08.015. Epub 2008 Aug 26.

多发性硬化症患者运动技能学习的保持。

Preservation of motor skill learning in patients with multiple sclerosis.

机构信息

Oxford Centre for Functional MRI of the Brain (FMRIB), Department of Clinical Neurology, University of Oxford, Oxford, UK.

出版信息

Mult Scler. 2011 Jan;17(1):103-15. doi: 10.1177/1352458510381257. Epub 2010 Sep 10.

DOI:10.1177/1352458510381257
PMID:20834040
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3671324/
Abstract

BACKGROUND

Several studies have demonstrated benefits of rehabilitation in multiple sclerosis (MS). However, the neuroscientific foundations for rehabilitation in MS are poorly established.

OBJECTIVES

As rehabilitation and motor learning share similar mechanisms of brain plasticity, we test whether the dynamics of skill learning are preserved in MS patients relative to controls.

METHODS

MS patients and controls learned a repeating sequence of hand movements and were assessed for short-term learning. Long-term learning was tested in another cohort of patients and controls practising the same sequence daily for two weeks.

RESULTS

Despite differences in baseline performance, the dynamics and extent of improvements were comparable between MS and control groups for both the short- and long-term learning. Even the most severely damaged patients were capable of performance improvements of similar magnitude to that seen in controls. After one week of training patients performed as well as the controls at baseline.

CONCLUSIONS

Mechanisms for short- and long-term plasticity may compensate for impaired functional connectivity in MS to mediate behavioural improvements. Future studies are needed to define the neurobiological substrates of this plasticity and the extent to which mechanisms of plasticity in patients may be distinct from those used for motor learning in controls.

摘要

背景

多项研究已经证明康复对多发性硬化症(MS)有多种益处。然而,MS 康复的神经科学基础尚未得到充分确立。

目的

由于康复和运动学习具有相似的大脑可塑性机制,我们测试了 MS 患者相对于对照组是否保留了技能学习的动态。

方法

MS 患者和对照组学习重复的手部运动序列,并评估短期学习情况。另一组患者和对照组则在两周内每天练习相同的序列,以测试长期学习。

结果

尽管基线表现存在差异,但 MS 和对照组在短期和长期学习中,改善的动态和程度相当。即使是受损最严重的患者,其表现改善的幅度也与对照组相似。经过一周的训练,患者的表现与对照组在基线时一样好。

结论

短期和长期可塑性的机制可能会补偿 MS 中功能连接的损伤,从而介导行为改善。未来的研究需要确定这种可塑性的神经生物学基础,以及患者的可塑性机制在多大程度上与对照组用于运动学习的机制不同。