电刺激受伤的神经促进动物和人类的恢复。

IF 4.7 2区 医学 Q1 NEUROSCIENCES Journal of Physiology-London Pub Date : 2024-12-22 DOI:10.1113/JP286566
Tessa Gordon
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引用次数: 0

摘要

延迟手术修复损伤的人类周围神经后,经常出现不良的功能结果,导致生长相关基因的进行性下调,同时在没有目标接触的神经元的慢性轴切、慢性远端神经残端去神经支配和慢性肌肉去神经支配的每种实验条件下,神经元再生能力也会降低。短暂(1小时)低频(20赫兹)电刺激(ES)加速了横断神经显微外科修复手术部位再生轴突的生长。运动项目也促进神经再生,其中ES和运动相结合是最有效的。完整神经(CES)的ES调节病变在手术修复远端神经损伤后加速轴突生长和再生速度,而修复的损伤神经的ES仅加速轴突生长。与仅加速轴突生长的修复损伤神经相比,在手术修复远端神经损伤后,CES加速了轴突生长和再生速度。马尾损伤患者的永久性失神经肌肉收缩力丧失,并伴有严重的肌肉质量损失,粗细可收缩纤维紊乱,以及控制钙向纤维输送的肌浆网紊乱,可通过为期2年的股四头肌每日ES计划得到缓解。这些发现为神经肌肉系统损伤患者的恢复和康复带来了希望。重点:慢性神经轴切术、自体神经移植物中的雪旺细胞去神经支配和肌肉去神经支配可以复制受损周围神经延迟手术修复后的不良功能结果。生长相关基因表达的指数下降伴随着再生能力的下降。短暂的(1小时)低频(20赫兹)电刺激(ES)产生动作电位传导到神经元体,即使在延迟手术后,也能加速横断神经手术修复部位再生轴突的生长。同样的ES方案可加速接受腕管综合征释放手术的慢性神经损伤患者的肌肉神经再生。一项为期2年的马尾损伤患者永久性失神经股四头肌每日ES计划恢复了其收缩性和组织。
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Electrical stimulation of injured nerves promotes recovery in animals and humans.

The frequent poor functional outcomes after delayed surgical repair of injured human peripheral nerves results in progressive downregulation of growth-associated genes in parallel with reduced neuronal regenerative capacity under each of the experimental conditions of chronic axotomy of neurones that remain without target contact, chronic distal nerve stump denervation, and chronic muscle denervation. Brief (1 h) low-frequency (20 Hz) electrical stimulation (ES) accelerates the outgrowth of regenerating axons across the surgical site of microsurgical repair of a transected nerve. Exercise programmes also promote nerve regeneration with the combination of ES and exercise being the most effective. An ES conditioning lesion of intact nerve (CES) accelerates both axonal outgrowth and regeneration rate after the surgical repair of a more distal injury to the nerve, in contrast to ES of a repaired injury nerve that accelerates only the axon outgrowth. A CES accelerates both axonal outgrowth and regeneration rate after the surgical repair of a more distal injury to the nerve, in contrast to ES of a repaired injury nerve that accelerates only the axon outgrowth. The loss of contractility of permanently denervated muscles in cauda equinae-injured patients with accompanying severe loss of muscle mass, disarray of thick and thin contractile filaments, and disorganization of the sarcoplasmic reticulum that controls calcium delivery to the filaments, is alleviated by a 2-year programme of daily ES of the quadriceps muscle. These findings hold promise for recovery and rehabilitation in patients who suffer injury to the neuromuscular system. KEY POINTS: Poor functional outcomes after delayed surgical repair of injured human peripheral nerves are replicated by chronic neuronal axotomy, Schwann cell denervation in a nerve autograft, and muscle denervation. Exponential decline in expression of growth-associated genes accompanies the same decline in regenerative capacity. Brief (1 h) low-frequency (20 Hz) electrical stimulation (ES) that generates action potential conduction to the neuronal soma accelerates the outgrowth of regenerating axons across the surgical repair site of the transected nerve, even after delayed surgery. The same ES regimen accelerates muscle reinnervation in patients with chronic nerve injury who undergo carpal tunnel syndrome release surgery. A 2-year programme of daily ES of permanently denervated quadriceps muscles in cauda equinae-injured patients reinstated their contractility and organization.

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来源期刊
Journal of Physiology-London
Journal of Physiology-London 医学-神经科学
CiteScore
9.70
自引率
7.30%
发文量
817
审稿时长
2 months
期刊介绍: The Journal of Physiology publishes full-length original Research Papers and Techniques for Physiology, which are short papers aimed at disseminating new techniques for physiological research. Articles solicited by the Editorial Board include Perspectives, Symposium Reports and Topical Reviews, which highlight areas of special physiological interest. CrossTalk articles are short editorial-style invited articles framing a debate between experts in the field on controversial topics. Letters to the Editor and Journal Club articles are also published. All categories of papers are subjected to peer reivew. The Journal of Physiology welcomes submitted research papers in all areas of physiology. Authors should present original work that illustrates new physiological principles or mechanisms. Papers on work at the molecular level, at the level of the cell membrane, single cells, tissues or organs and on systems physiology are all acceptable. Theoretical papers and papers that use computational models to further our understanding of physiological processes will be considered if based on experimentally derived data and if the hypothesis advanced is directly amenable to experimental testing. While emphasis is on human and mammalian physiology, work on lower vertebrate or invertebrate preparations may be suitable if it furthers the understanding of the functioning of other organisms including mammals.
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