Optogenetic Neuronal Stimulation Promotes Functional Recovery After Spinal Cord Injury

• Published in: Frontiers in neuroscience Vol. 15; p. 640255
• Main Authors: Deng, Wei-Wei, Wu, Guang-Yan, Min, Ling-Xia, Feng, Zhou, Chen, Hui, Tan, Ming-Liang, Sui, Jian-Feng, Liu, Hong-Liang, Hou, Jing-Ming
• Format: Journal Article
• Language: English
• Published: Switzerland Frontiers Research Foundation 09.04.2021; Frontiers Media S.A
• Subjects: Animals; Brain research; Brain-derived neurotrophic factor; Clinical trials; Cortex (motor); Excitability; functional recovery; GAP-43 protein; glutaminergic neurons; Lasers; Light; Medical research; motor cortex; Motor evoked potentials; Nerve growth factor; Neurons; Neuroscience; optogenetics; Recovery of function; Spinal cord injuries; spinal cord injury; Transcranial magnetic stimulation; China; spinal cord injury; motor cortex; functional recovery; glutaminergic neurons; optogenetics
• ISSN: 1662-4548; 1662-453X; 1662-453X
• DOI: 10.3389/fnins.2021.640255

Although spinal cord injury (SCI) is the main cause of disability worldwide, there is still no definite and effective treatment method for this condition. Our previous clinical trials confirmed that the increased excitability of the motor cortex was related to the functional prognosis of patients with SCI. However, it remains unclear which cell types in the motor cortex lead to the later functional recovery. Herein, we applied optogenetic technology to selectively activate glutamate neurons in the primary motor cortex and explore whether activation of glutamate neurons in the primary motor cortex can promote functional recovery after SCI in rats and the preliminary neural mechanisms involved. Our results showed that the activation of glutamate neurons in the motor cortex could significantly improve the motor function scores in rats, effectively shorten the incubation period of motor evoked potentials and increase motor potentials' amplitude. In addition, hematoxylin-eosin staining and nerve fiber staining at the injured site showed that accurate activation of the primary motor cortex could effectively promote tissue recovery and neurofilament growth (GAP-43, NF) at the injured site of the spinal cord, while the content of some growth-related proteins (BDNF, NGF) at the injured site increased. These results suggested that selective activation of glutamate neurons in the primary motor cortex can promote functional recovery after SCI and may be of great significance for understanding the neural cell mechanism underlying functional recovery induced by motor cortex stimulation.