同时使用脑脊髓功能MRI绘制手功能图。

Imaging neuroscience (Cambridge, Mass.) Pub Date : 2025-10-03 eCollection Date: 2025-01-01 DOI:10.1162/IMAG.a.159
Valeria Oliva, Sandrine Bédard, Merve Kaptan, Dario Pfyffer, Brett Chy, Susanna Aufrichtig, Nazrawit Berhe, Akshay S Chaudhari, Suzanne Tharin, Serena S Hu, John Ratliff, Zachary A Smith, Andrew C Smith, Gary H Glover, Sean Mackey, Christine S W Law, Kenneth A Weber Ii
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引用次数: 0

摘要

手部运动控制依赖于复杂的脑脊髓相互作用,从而调节肌肉活动。脑、脊髓和周围神经的损伤可导致手的功能受损,从而导致虚弱和协调性受损。功能磁共振成像(fMRI)可以绘制运动相关的神经活动,并可能表征手无力和协调能力下降的机制。尽管脑运动控制已被广泛研究,脊髓机制仍较少探索。在这里,我们同时使用脑脊髓功能磁共振成像来绘制中枢神经系统中与手的力量和灵活性相关的神经活动,使用力量匹配和手指敲击任务。我们使用3T GE扫描仪对28名右撇子健康志愿者(年龄:40.0±13.8岁,女14名,男14名)同时进行脑脊髓功能磁共振成像。参与者在最大自愿收缩的10%、20%和30%时执行力匹配任务。对于手指敲击任务,参与者完成三个任务级别的按键:只有第二个数字的单位数反应,所有数字按顺序的单位数反应,以及所有数字按随机顺序的单位数反应。脑和脊髓图像分别处理,并评估激活和失活。还进行了兴趣区域(ROI)分析,以探索跨任务级别激活的局部变化。两项任务都激发了大脑和脊髓的运动和感觉区域的激活,在不同的任务水平上,左初级运动(M1)、左初级感觉(S1)皮层和右脊髓灰质的反应是分级的。右侧M1和S1的失活也出现在这两个任务中。在力匹配任务中,左侧脊髓灰质失活与任务水平成比例。ROI分析结果补充了组级活动图。我们的研究提供了手功能中脑脊髓相互作用的详细图谱,揭示了运动和感觉区域的神经激活和失活模式。右侧M1失活可能是单侧任务中限制外部运动输出的半球间抑制的证据。对于力匹配,脊髓左腹角和背角的失活提供了第一个证据,证明单侧运动任务中运动区域的抑制延伸到脊髓。这种抑制是否来自大脑的直接下行调节或脊髓的神经元间抑制仍有待研究。这些发现扩大了我们对中枢运动控制机制的理解,并可以为运动障碍患者的康复策略提供信息。这种方法可能为研究中风、脊髓损伤和神经退行性疾病等情况下的运动功能障碍提供基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Mapping hand function with simultaneous brain-spinal cord functional MRI.

Hand motor control depends on intricate brain-spinal cord interactions that regulate muscle activity. Hand function can be disrupted by injury to the brain, spinal cord, and peripheral nerves leading to weakness and impaired coordination. Functional MRI (fMRI) can map motor-related neural activity and potentially characterize the mechanisms underlying hand weakness and diminished coordination. Although brain motor control has been extensively studied, spinal cord mechanisms remain less explored. Here we use simultaneous brain-spinal cord fMRI to map neural activity related to hand strength and dexterity across the central nervous system using force matching and finger tapping tasks. We performed simultaneous brain-spinal cord fMRI in 28 right-handed healthy volunteers (age: 40.0 ± 13.8 years, 14 females, 14 males) using a 3T GE scanner. Participants performed a force-matching task at 10%, 20%, and 30% of maximum voluntary contraction. For the finger tapping task, participants completed button presses for three task levels: single-digit response with the second digit only, single-digit response with all digits in a sequential order, and single-digit response with all digits in a random order. Brain and spinal cord images were processed separately and assessed both activations and deactivations. Region of interest (ROI) analyses were also conducted to explore localized changes in activation across the task levels. Both tasks elicited activation in motor and sensory regions of the brain and spinal cord, with graded responses in the left primary motor (M1), left primary sensory (S1) cortex, and right spinal cord gray matter across task levels. Deactivation of the right M1 and S1 was also present for both tasks. Deactivation of the left spinal cord gray matter that scaled with task level was seen in the force matching task. The ROI analysis findings complemented the group level activity maps. Our study provides a detailed map of brain-spinal cord interactions in hand function, revealing graded neural activation and deactivation patterns across motor and sensory regions. Right M1 deactivation is likely evidence of interhemispheric inhibition that restricts extraneous motor output during unilateral tasks. For force matching, the deactivation of the left ventral and dorsal horns of the spinal cord provides the first evidence that the inhibition of motor areas during a unilateral motor task extends to the spinal cord. Whether this inhibition results from direct descending modulation from the brain or interneuronal inhibition in the spinal cord remains to be interrogated. These findings expand our understanding of central motor control mechanisms and could inform rehabilitation strategies for individuals with motor impairments. This approach may offer a foundation for studying motor dysfunction in conditions such as stroke, spinal cord injury, and neurodegenerative diseases.

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