Hachmann Jan T, Jeong Ju Ho, Grahn Peter J, Mallory Grant W, Evertz Loribeth Q, Bieber Allan J, Lobel Darlene A, Bennet Kevin E, Lee Kendall H, Lujan J Luis
Department of Neurologic Surgery, Mayo Clinic, Rochester, Minnesota, United States of America ; Mayo Graduate School, Mayo Clinic, Rochester, Minnesota, United States of America.
PLoS One. 2013 Dec 5;8(12):e81443. doi: 10.1371/journal.pone.0081443. eCollection 2013.
Restoration of movement following spinal cord injury (SCI) has been achieved using electrical stimulation of peripheral nerves and skeletal muscles. However, practical limitations such as the rapid onset of muscle fatigue hinder clinical application of these technologies. Recently, direct stimulation of alpha motor neurons has shown promise for evoking graded, controlled, and sustained muscle contractions in rodent and feline animal models while overcoming some of these limitations. However, small animal models are not optimal for the development of clinical spinal stimulation techniques for functional restoration of movement. Furthermore, variance in surgical procedure, targeting, and electrode implantation techniques can compromise therapeutic outcomes and impede comparison of results across studies. Herein, we present a protocol and large animal model that allow standardized development, testing, and optimization of novel clinical strategies for restoring motor function following spinal cord injury. We tested this protocol using both epidural and intraspinal stimulation in a porcine model of spinal cord injury, but the protocol is suitable for the development of other novel therapeutic strategies. This protocol will help characterize spinal circuits vital for selective activation of motor neuron pools. In turn, this will expedite the development and validation of high-precision therapeutic targeting strategies and stimulation technologies for optimal restoration of motor function in humans.
通过对周围神经和骨骼肌进行电刺激,已实现脊髓损伤(SCI)后运动功能的恢复。然而,诸如肌肉疲劳快速出现等实际限制阻碍了这些技术的临床应用。最近,在啮齿动物和猫科动物模型中,直接刺激α运动神经元已显示出在引发分级、可控和持续肌肉收缩方面的前景,同时克服了其中一些限制。然而,小型动物模型对于开发用于运动功能恢复的临床脊髓刺激技术并非最佳选择。此外,手术程序、靶点和电极植入技术的差异可能会影响治疗效果,并妨碍不同研究结果之间的比较。在此,我们介绍一种方案和大型动物模型,可用于标准化开发、测试和优化脊髓损伤后恢复运动功能的新型临床策略。我们在猪脊髓损伤模型中使用硬膜外刺激和脊髓内刺激对该方案进行了测试,但该方案适用于开发其他新型治疗策略。该方案将有助于确定对运动神经元池选择性激活至关重要的脊髓回路特征。反过来,这将加快高精度治疗靶向策略和刺激技术的开发与验证,以实现人类运动功能的最佳恢复。