中国神经再生研究(英文版) ›› 2026, Vol. 21 ›› Issue (8): 3336-3348.doi: 10.4103/NRR.NRR-D-25-00553

• 综述:脊髓损伤修复保护与再生 • 上一篇    下一篇

脊髓刺激术:脊髓损伤后慢性疼痛缓解的新兴策略

  

  • 出版日期:2026-08-18 发布日期:2026-04-23
  • 基金资助:
    辽宁省教育厅重点攻关项目(2024C011)及大连医科大学第一附属医院与大连化学物理研究所医产联合创新基金项目(DMU-1&DICP UN202311)

Spinal cord stimulation: emerging strategy for chronic pain relief after spinal cord injury

Qiwen Wang1, #, Ying Zhang1, 2, #, Huifeng Zhang1, 2, Zhonghai Li1, *   

  1. 1Department of Orthopedics, First Affiliated Hospital of Dalian Medical University, Dalian, Liaoning Province, China; 
    2Dalian Medical University, Dalian, Liaoning Province, China
  • Online:2026-08-18 Published:2026-04-23
  • Contact: Zhonghai Li, PhD, lizhonghaispine@126.com.
  • Supported by:
    This work was supported by Key Tackling Project of the Education Department of Liaoning Province, No. 2024C011; and the Medical-Industrial Joint Innovation Funding Project of the First Hospital of Dalian Medical University and Dalian Institute of Chemical Physics, No. DMU-1&DICP UN202311 (both to ZL).

摘要:

 脊髓损伤后的慢性疼痛指的是在脊髓损伤后持续或反复出现的疼痛,表现为灼烧感、刺痛感和电击感。近期多项研究表明,脊髓刺激是治疗脊髓损伤后慢性疼痛的有效方法。文章的目的是介绍脊髓刺激技术、脊髓损伤的临床表现以及脊髓刺激在脊髓损伤治疗中的作用,并讨论脊髓刺激在治疗脊髓损伤后疼痛中的机制及临床应用情况。脊髓刺激的机制主要涉及3个方面:神经调控、神经化学调节以及抗炎和神经修复作用。在神经调控方面,脊髓刺激基于疼痛的闸门控制理论,它通过激活大直径Aβ神经纤维,促进脊髓中γ-氨基丁酸(GABA)能抑制性中间神经元释放抑制性神经递质,从而阻断小直径C纤维传递的疼痛信号。神经化学研究表明,脊髓刺激可调节脊髓内神经递质的平衡,增加抑制性神经递质(如GABA、血清素和乙酰胆碱)的释放,同时降低兴奋性神经递质的水平。此外,脊髓刺激还具有显著的抗炎和神经保护作用,可下调促炎因子水平、上调抗炎因子表达、缓解神经炎症反应,并通过促进神经营养因子的分泌和轴突再生修复受损的神经回路。因此,脊髓刺激在脊髓损伤后疼痛的临床治疗中已展现出显著疗效,但仍存在局限性,如仍存在临床研究样本量较小且异质性高,以及长期疗效数据不足的缺陷。未来研究应开展多中心大样本随机对照试验,并建立长期随访机制以提升循证医学证据。


https://orcid.org/0000-0003-4735-1193 (Zhonghai Li)

关键词: 慢性疼痛, 电刺激疗法, γ-氨基丁酸能神经元, 神经炎症性疾病, 神经病理性疼痛, 神经可塑性, 神经保护, 疼痛管理, 脊髓损伤, 脊髓刺激

Abstract: Chronic pain following a spinal cord injury refers to pain that persists or recurs after the injury. This pain can manifest as burning, stinging, or sensations similar to electric shocks. Recent studies have shown that spinal cord stimulation is an effective way to treat chronic pain after spinal cord injury. The purpose of this review is to introduce the technique of spinal cord stimulation, the clinical manifestations of spinal cord injury, and the role of spinal cord stimulation in the treatment of spinal cord injury. The mechanism and clinical application of spinal cord stimulation in the treatment of pain after spinal cord injury are discussed. The mechanism of spinal cord stimulation primarily involves three aspects: neuromodulation, neurochemical regulation, and anti-inflammatory effects, along with nerve repair. In terms of neuromodulation, spinal cord stimulation is based on the gate control theory of pain. It activates large-diameter Aβ nerve fibers to promote the release of inhibitory neurotransmitters by gamma-aminobutyric acidergic inhibitory interneurons in the spinal cord, thereby blocking the transmission of pain signals from small-diameter C fibers. Neurochemical studies indicate that spinal cord stimulation can regulate the balance of neurotransmitters within the spinal cord, increasing the release of inhibitory neurotransmitters such as gamma-aminobutyric acid, serotonin, and acetylcholine while reducing the levels of excitatory neurotransmitters. Additionally, spinal cord stimulation exhibits significant anti-inflammatory and neuroprotective effects, downregulating pro-inflammatory factor levels, upregulating anti-inflammatory factor expression, alleviating neuroinflammatory responses, and repairing damaged neural circuits by promoting the secretion of neurotrophic factors and axonal regeneration. Spinal cord stimulation have demonstrated remarkable efficacy in the clinical treatment of pain after spinal cord injury, but there are still limitations such as small sample size and high heterogeneity in clinical studies, as well as insufficient long-term efficacy data. Future research should conduct multi-center large-sample randomized controlled trials, and establish long-term follow-up mechanisms to improve evidence-based medical evidence.

Key words: chronic pain, electric stimulation therapy, GABAergic neurons, nerve regeneration, neuroinflammatory diseases, neuronal plasticity, neuropathic pain, neuroprotection, pain management, spinal cord injuries, spinal cord stimulation