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在体显示人类皮质脊髓束的微观结构躯体定位图谱。

In vivo mapping of microstructural somatotopies in the human corticospinal pathways.

机构信息

Learning Research and Development Center, University of Pittsburgh, 3939 O'Hara St., Pittsburgh, PA 15260, USA.

出版信息

J Neurophysiol. 2011 Jan;105(1):336-46. doi: 10.1152/jn.00698.2010. Epub 2010 Nov 10.

DOI:10.1152/jn.00698.2010
PMID:21068263
Abstract

The human corticospinal pathway is organized in a body-centric (i.e., somatotopic) manner that begins in cortical cell bodies and is maintained in the axons as they project through the midbrain on their way to spinal motor neurons. The subcortical segment of this somatotopy has been described using histological methods on non-human primates but only coarsely validated from lesion studies in human patient populations. Using high definition fiber tracking (HDFT) techniques, we set out to provide the first in vivo quantitative description of the midbrain somatotopy of corticospinal fibers in humans. Multi-shell diffusion imaging and deterministic fiber tracking were used to map white matter bundles that originate in the neocortex, navigate complex fiber crossings, and project through the midbrain. These fiber bundles were segmented into premotor (dorsal premotor, ventral premotor, and supplementary motor area) and primary motor sections based on the cortical origin of each fiber streamline. With HDFT, we were able to reveal several unique corticospinal patterns, including the cortical origins of ventral premotor fibers and small (∼ 1-2 mm) shifts in the midbrain location of premotor versus primary motor cortex fibers. More importantly, within the relatively small diameter of the pyramidal tracts (∼ 5 mm), we were able to map and quantify the direction of the corticospinal somatotopy. These results show how an HDFT approach to white matter mapping provides the first in vivo, quantitative mapping of subcortical corticospinal topographies at resolutions previously only available with postmortem histological techniques.

摘要

人类皮质脊髓通路以身体为中心(即躯体定位)的方式组织,从皮质细胞体开始,并在轴突中保持,因为它们从中脑投射到脊髓运动神经元。使用非人类灵长类动物的组织学方法已经描述了这种躯体定位的皮质下节段,但仅在人类患者群体的病变研究中进行了粗略验证。使用高清晰度纤维跟踪 (HDFT) 技术,我们旨在提供人类皮质脊髓纤维中脑躯体定位的第一个体内定量描述。多壳扩散成像和确定性纤维跟踪用于绘制起源于新皮质的白质束,这些白质束在穿过中脑时会进行复杂的纤维交叉。这些纤维束根据每条纤维流线的皮质起源分为运动前区(背侧运动前区、腹侧运动前区和补充运动区)和初级运动区。通过 HDFT,我们能够揭示出几种独特的皮质脊髓模式,包括腹侧运动前纤维的皮质起源以及运动前区和初级运动区纤维在中脑位置的微小(约 1-2 毫米)变化。更重要的是,在相对较小的锥体束直径(约 5 毫米)内,我们能够绘制和量化皮质脊髓躯体定位的方向。这些结果表明,HDFT 方法如何对白质进行映射,从而以前仅通过死后组织学技术才能实现的分辨率提供了体内亚皮质皮质脊髓地形图的首次定量映射。

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