Uramaru Koichi, Abe Hiroki, Nakajima Waki, Ota Wataru, Suzuki Michiaki, Yokoyama Osamu, Yamamoto Tetsuya, Nishimura Yukio, Takahashi Takuya
Department of Physiology, Yokohama City University Graduate School of Medicine, Yokohama 236-0004, Japan.
Department of Neurosurgery, Yokohama City University Graduate School of Medicine, Yokohama 236-0004, Japan.
Brain Commun. 2025 Mar 13;7(2):fcaf036. doi: 10.1093/braincomms/fcaf036. eCollection 2025.
While spinal cord injury (SCI) aggravates the quality of life in humans by severe paralysis, clinical intervention to promote functional recovery from SCI is limited. We recently identified a small compound, edonerpic maleate (edonerpic MA), which accelerates training-dependent motor functional recovery from brain damage in rodents (cryo-genic cortical injury) and non-human primates (internal capsule haemorrhage) by the facilitation of experience-dependent synaptic trafficking of glutamate α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptors. In the present study, we investigated whether edonerpic MA accelerates functional recovery after SCI in non-human primates. Six adult monkeys () received a unilateral SCI between the C6 and C7 segment. After the SCI, upper limb motor function was immediately impaired and the animals were assigned to receive vehicle ( = 3) or 3 mg/kg/day edonerpic maleate ( = 3) by intramuscular injection for 2 months. The rehabilitative training and evaluation of behaviour using the slit task were performed 5 days a week for 2 months after SCI. The edonerpic MA-treated group showed significantly improved grasping movements than the control group. After recovery reached a plateau, we examined the somatotopic map of the contralesional primary motor cortex (M1) using intracortical microstimulation. The motor representation of wrist territory at contralesional M1 was larger in the edonerpic MA-treated group than in the control group. We concluded that edonerpic MA accelerates the recovery of grasping movements after SCI, accompanied by cortical somatotopic reorganization. Since edonerpic MA enhances recovery from damage in the central nervous system at multiple levels, treatment with edonerpic MA combined with rehabilitative training may represent a novel therapy for not only stroke but also for SCI.
虽然脊髓损伤(SCI)通过严重瘫痪降低了人类的生活质量,但促进SCI功能恢复的临床干预措施有限。我们最近发现了一种小分子化合物,马来酸依度那匹(edonerpic MA),它通过促进依赖经验的谷氨酸α-氨基-3-羟基-5-甲基-4-异恶唑丙酸受体的突触转运,加速了啮齿动物(低温性皮质损伤)和非人类灵长类动物(内囊出血)脑损伤后依赖训练的运动功能恢复。在本研究中,我们调查了马来酸依度那匹是否能加速非人类灵长类动物SCI后的功能恢复。六只成年猴子()在C6和C7节段之间接受了单侧SCI。SCI后,上肢运动功能立即受损,动物被分配接受载体(=3)或通过肌肉注射给予3mg/kg/天的马来酸依度那匹(=3),持续2个月。SCI后每周5天进行康复训练,并使用狭缝任务对行为进行评估,持续2个月。马来酸依度那匹治疗组的抓握动作明显比对照组改善。恢复达到平台期后,我们使用皮质内微刺激检查了对侧初级运动皮层(M1)的躯体定位图。马来酸依度那匹治疗组对侧M1处腕部区域的运动代表区比对照组大。我们得出结论,马来酸依度那匹加速了SCI后抓握动作的恢复,并伴有皮质躯体定位重组。由于马来酸依度那匹在多个水平上增强了中枢神经系统损伤后的恢复,马来酸依度那匹联合康复训练治疗不仅可能是中风的一种新疗法,也可能是SCI的新疗法。