Department of Neurosurgery, Center for Translational Neural Prosthetics and Interfaces, Houston Methodist Research Institute, 6550 Fannin Street, Houston, TX 77030, United States; Department of Neurosurgery, Center for Neuroregeneration, Houston Methodist Research Institute, 6550 Fannin Street, Houston, TX 77030, United States.
Department of Neurosurgery, Center for Translational Neural Prosthetics and Interfaces, Houston Methodist Research Institute, 6550 Fannin Street, Houston, TX 77030, United States; Neuroscience Department, International School for Advanced Studies (SISSA), Bonomea, Trieste, Italy.
J Neurosci Methods. 2024 May;405:110104. doi: 10.1016/j.jneumeth.2024.110104. Epub 2024 Mar 5.
Preclinical models are essential for identifying changes occurring after neurologic injury and assessing therapeutic interventions. Yucatan miniature pigs (minipigs) have brain and spinal cord dimensions like humans and are useful for laboratory-to-clinic studies. Yet, little work has been done to map spinal sensorimotor distributions and identify similarities and differences between the porcine and human spinal cords.
To characterize efferent and afferent signaling, we implanted a conventional 32-contact, four-column array into the dorsal epidural space over the lumbosacral spinal cord, spanning the L5-L6 vertebrae, in two Yucatan minipigs. Spinally evoked motor potentials were recorded bilaterally in four hindlimb muscles during stimulation delivered from different array locations. Then, cord dorsum potentials were recorded via the array by stimulating the left and right tibial nerves.
Utilizing epidural spinal stimulation, we achieved selective left, right, proximal, and distal activation in the hindlimb muscles. We then determined the selectivity of each muscle as a function of stimulation location which relates to the distribution of the lumbar motor pools.
Mapping motoneuron distribution to hindlimb muscles and recording responses to peripheral nerve stimulation in the dorsal epidural space reveals insights into ascending and descending signal propagation in the lumbar spinal cord. Clinical-grade arrays have not been utilized in a porcine model.
These results indicate that efferent and afferent spinal sensorimotor networks are spatially distinct, provide information about the organization of motor pools in the lumbar enlargement, and demonstrate the feasibility of using clinical-grade devices in large animal research.
临床前模型对于识别神经损伤后发生的变化和评估治疗干预措施至关重要。尤卡坦小型猪(迷你猪)的大脑和脊髓尺寸与人类相似,可用于实验室到临床的研究。然而,很少有研究致力于绘制脊髓感觉运动分布图谱,并确定猪和人类脊髓之间的相似性和差异性。
为了描述传出和传入信号,我们将传统的 32 个接触点、四列阵列植入到两个尤卡坦迷你猪的腰骶部背侧硬膜外腔,跨越 L5-L6 椎骨。在刺激来自不同阵列位置时,双侧后肢肌肉记录到脊髓诱发的运动电位。然后,通过刺激左右胫神经,通过阵列记录脊髓背侧电位。
利用硬膜外脊髓刺激,我们实现了对后肢肌肉的选择性左、右、近和远侧激活。然后,我们根据刺激位置确定了每个肌肉的选择性,这与腰运动池的分布有关。
将运动神经元分布映射到后肢肌肉,并记录背侧硬膜外空间中对周围神经刺激的反应,揭示了对腰椎脊髓中上行和下行信号传播的深入了解。临床级别的阵列尚未在猪模型中得到应用。
这些结果表明,传出和传入的脊髓感觉运动网络在空间上是不同的,提供了关于腰膨大运动池组织的信息,并证明了在大型动物研究中使用临床级设备的可行性。