晚期髓鞘形成的活动调节是人类神经系统中的一种可塑性机制吗?

Neuron glia biology Pub Date : 2009-05-01 Epub Date: 2009-09-29 DOI:10.1017/S1740925X09990330
Fredrik Ullén
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引用次数: 60

摘要

各种动物模型的研究表明,神经元活动可以影响髓鞘形成过程。这种机制是否存在于人类中,它们是否不仅在早期发育中,而且在青少年和成人中调解经验驱动的白质可塑性?虽然目前还没有直接的证据证明这一点,但这里回顾的一些发现与这一观点是一致的。首先,尸检和神经成像研究表明,人类白质的发育是一个漫长的过程,一直持续到成年。第二,白质结构的发育变化和个体差异与神经活动和行为的差异有关。最后,对长期训练效果的研究,特别是对音乐家的研究,表明了训练和白质结构之间的密切关系。最后,我简要地讨论了可能支持这些发现的白质可塑性的类型,强调了间接髓鞘形成可塑性(髓鞘与轴突本身平行生长)和直接髓鞘形成可塑性(髓鞘厚度独立于轴突直径调节)之间的区别。
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Is activity regulation of late myelination a plastic mechanism in the human nervous system?

Studies on various animal models have established that neuronal activity can influence the myelination process. Are such mechanisms present in humans, and do they mediate experience-driven white matter plasticity not only during early development but also in adolescents and adults? While there is as yet no direct evidence for this, a number of findings - reviewed here - are consistent with this idea. First, postmortem and neuroimaging studies show that the human white matter development is a protracted process that continues well into adulthood. Second, developmental changes and individual differences in white matter structure are related to differences in neural activity and behavior. Finally, studies on effects of long-term training, in particular in musicians, show strong relations between training and white matter structure. I conclude by briefly discussing possible types of white matter plasticity that could underlie these findings, emphasizing a distinction between indirect myelination plasticity, where the myelin sheath grows in parallel with the axon itself, and direct myelination plasticity, where the myelin sheath thickness is modulated independently of axonal diameter.

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Neuron glia biology
Neuron glia biology 医学-神经科学
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