Oliva Valeria, Bédard Sandrine, Kaptan Merve, Pfyffer Dario, Chy Brett, Aufrichtig Susanna, Berhe Nazrawit, Chaudhari Akshay S, Tharin Suzanne, Hu Serena S, Ratliff John, Smith Zachary A, Smith Andrew C, Glover Gary H, Mackey Sean, Law Christine S W, Weber Kenneth A
bioRxiv. 2025 Feb 27:2025.02.27.640504. doi: 10.1101/2025.02.27.640504.
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. This study pioneers the use of simultaneous brain-spinal cord fMRI to comprehensively map hand function, offering novel insights into coordinated motor processing across the central nervous system.
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 SIGNA Premier scanner equipped with a 21-channel head-neck coil. Participants performed a force-matching task at 10%, 20%, and 30% of maximum voluntary contraction using a hand dynamometer. For the finger tapping task, participants completed button-presses at 1 Hz with a 5-button response pad for three task levels: single-digit response with the second digit only (low), single-digit response with all digits in a sequential order (medium), single-digit response with all digits in a random order (high). Visual cues and feedback were provided during the tasks.Brain and spinal cord images were processed separately using FSL and the Spinal Cord Toolbox, with motion correction, physiological noise filtering, and spatial normalization to standard templates. Subject level activity maps were generated and entered into group level analyses to explore both activations and deactivations. For the brain, we used a mixed effect design with a voxelwise threshold of Z score > 3.10 and cluster threshold of p < 0.05. For the spinal cord, we used a fixed effect design with a voxelwise threshold of Z score > 1.64 and cluster threshold of p < 0.05. Region of interest (ROI) analyses were conducted to examine localized changes in activation across 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 was present in the high task level of 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 inhibition patterns across motor and sensory regions. Interhemispheric inhibition, reflected in right M1 deactivation, likely 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 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.
Our simultaneous brain-spinal cord fMRI approach provides novel insights into the neural coordination of hand function, enhancing our understanding of motor control and its modulation. This approach may offer a foundation for studying motor dysfunction in conditions such as stroke, spinal cord injury, and neurodegenerative diseases.
手部运动控制依赖于调节肌肉活动的复杂脑 - 脊髓相互作用。脑、脊髓和周围神经的损伤会破坏手部功能,导致无力和协调性受损。功能磁共振成像(fMRI)可以绘制与运动相关的神经活动图,并有可能表征手部无力和协调性下降的潜在机制。尽管脑运动控制已得到广泛研究,但脊髓机制仍有待进一步探索。在这里,我们使用同步脑 - 脊髓fMRI,通过力量匹配和手指敲击任务来绘制整个中枢神经系统中与手部力量和灵活性相关的神经活动图。本研究率先使用同步脑 - 脊髓fMRI全面绘制手部功能图,为中枢神经系统的协调运动处理提供了新的见解。
我们使用配备21通道头颈线圈的3T GE SIGNA Premier扫描仪,对28名右利手健康志愿者(年龄:40.0±13.8岁,14名女性,14名男性)进行了同步脑 - 脊髓fMRI检查。参与者使用握力计在最大自主收缩的10%、20%和30%水平上执行力量匹配任务。对于手指敲击任务,参与者使用5键响应垫以1Hz的频率完成按键操作,共有三个任务水平:仅用食指进行单指响应(低)、按顺序用所有手指进行单指响应(中)、随机用所有手指进行单指响应(高)。任务过程中提供视觉提示和反馈。脑和脊髓图像分别使用FSL和脊髓工具箱进行处理,包括运动校正、生理噪声滤波以及对标准模板的空间归一化。生成个体水平的活动图并进行组水平分析,以探索激活和去激活情况。对于脑,我们采用混合效应设计,体素水平阈值为Z分数>3.10,聚类阈值为p<0.05。对于脊髓,我们采用固定效应设计,体素水平阈值为Z分数>1.64,聚类阈值为p<0.05。进行感兴趣区域(ROI)分析以检查各任务水平下激活的局部变化。
两项任务均在脑和脊髓的运动和感觉区域引发激活,在整个任务水平上,左侧初级运动皮层(M1)、左侧初级感觉皮层(S1)和右侧脊髓灰质呈现分级反应。两项任务中右侧M1和S1也出现去激活。在力量匹配任务的高任务水平中,左侧脊髓灰质出现去激活。ROI分析结果补充了组水平的活动图。
我们的研究提供了手部功能中脑 - 脊髓相互作用的详细图谱,揭示了运动和感觉区域的分级神经激活和抑制模式。右侧M1去激活所反映的半球间抑制可能在单侧任务中限制了无关的运动输出。对于力量匹配,脊髓左侧腹角和背角的去激活首次证明了单侧运动任务期间运动区域的抑制延伸至脊髓。这种抑制是由脑的直接下行调制还是脊髓中的中间神经元抑制导致,仍有待研究。这些发现扩展了我们对中枢运动控制机制的理解,并可为运动障碍个体的康复策略提供参考。
我们的同步脑 - 脊髓fMRI方法为手部功能的神经协调提供了新的见解,增强了我们对运动控制及其调节的理解。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。