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Combination Intrathecal Drug Therapy Strategies for Pain Management.鞘内药物治疗联合策略用于疼痛管理。
Pain Physician. 2021 Dec;24(8):549-569.
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LncRNA NEAT1/miR-128-3p/AQP4 axis regulating spinal cord injury-induced neuropathic pain progression.长链非编码 RNA NEAT1/miR-128-3p/AQP4 轴调控脊髓损伤诱导的神经性疼痛进展。
J Neuroimmunol. 2021 Feb 15;351:577457. doi: 10.1016/j.jneuroim.2020.577457. Epub 2020 Dec 9.
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Knockdown of miR-130a-3p alleviates spinal cord injury induced neuropathic pain by activating IGF-1/IGF-1R pathway.敲低 miR-130a-3p 通过激活 IGF-1/IGF-1R 通路缓解脊髓损伤诱导的神经性疼痛。
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Intrathecal Drug Delivery for Chronic Pain Syndromes: A Review of Considerations in Practice Management.鞘内药物递送治疗慢性疼痛综合征:实践管理中的注意事项综述。
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Intrathecal Injection of SIRT1-modified Human Mesenchymal Stem Cells Alleviates Neuropathic Pain in Rat.鞘内注射 SIRT1 修饰的人骨髓间充质干细胞缓解大鼠神经病理性疼痛。
J Mol Neurosci. 2021 May;71(5):972-980. doi: 10.1007/s12031-020-01717-2. Epub 2020 Oct 2.
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Chronic Pain After Spinal Cord Injury: Is There a Role for Neuron-Immune Dysregulation?脊髓损伤后的慢性疼痛:神经元-免疫失调是否起作用?
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Modulation of neuroglial interactions using differential target multiplexed spinal cord stimulation in an animal model of neuropathic pain.使用针对不同靶点的脊髓刺激的方法调节神经胶质细胞相互作用,建立神经性疼痛动物模型。
Mol Pain. 2020 Jan-Dec;16:1744806920918057. doi: 10.1177/1744806920918057.
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Simultaneous intrathecal injection of muscimol and endomorphin-1 alleviates neuropathic pain in rat model of spinal cord injury.鞘内注射 muscimol 和内吗啡肽-1 缓解脊髓损伤大鼠模型的神经病理性疼痛。
Brain Behav. 2020 May;10(5):e01576. doi: 10.1002/brb3.1576. Epub 2020 Mar 18.
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The long-term analgesic effect of intrathecal baclofen on neuropathic pain in patients with spinal cord injury.鞘内注射巴氯芬对脊髓损伤患者神经性疼痛的长期镇痛效果。
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Glia to neuron ratio in the posterior aspect of the human spinal cord at thoracic segments relevant to spinal cord stimulation.人类胸段脊髓与脊髓刺激相关的后角神经胶质与神经元比值。
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脊髓损伤后神经病理性疼痛鞘内管理的新证据

Emerging Evidence for Intrathecal Management of Neuropathic Pain Following Spinal Cord Injury.

作者信息

Karri Jay, Doan James, Vangeison Christian, Catalanotto Marissa, Nagpal Ameet S, Li Sheng

机构信息

Division of Pain Medicine, Department of Anesthesiology and Critical Care Medicine, Johns Hopkins University School of Medicine, Baltimore, MD, United States.

Department of Physical Medicine and Rehabilitation, Harvard Medical School, Boston, MA, United States.

出版信息

Front Pain Res (Lausanne). 2022 Jul 28;3:933422. doi: 10.3389/fpain.2022.933422. eCollection 2022.

DOI:10.3389/fpain.2022.933422
PMID:35965596
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9371595/
Abstract

A high prevalence of patients with spinal cord injury (SCI) suffer from chronic neuropathic pain. Unfortunately, the precise pathophysiological mechanisms underlying this phenomenon have yet to be clearly elucidated and targeted treatments are largely lacking. As an unfortunate consequence, neuropathic pain in the population with SCI is refractory to standard of care treatments and represents a significant contributor to morbidity and suffering. In recent years, advances from SCI-specific animal studies and translational models have furthered our understanding of the neuronal excitability, glial dysregulation, and chronic inflammation processes that facilitate neuropathic pain. These developments have served advantageously to facilitate exploration into the use of neuromodulation as a treatment modality. The use of intrathecal drug delivery (IDD), with novel pharmacotherapies, to treat chronic neuropathic pain has gained particular attention in both pre-clinical and clinical contexts. In this evidence-based narrative review, we provide a comprehensive exploration into the emerging evidence for the pathogenesis of neuropathic pain following SCI, the evidence basis for IDD as a therapeutic strategy, and novel pharmacologics across impactful animal and clinical studies.

摘要

脊髓损伤(SCI)患者中慢性神经性疼痛的患病率很高。不幸的是,这一现象背后的确切病理生理机制尚未完全阐明,而且在很大程度上缺乏针对性的治疗方法。因此,SCI患者群体中的神经性疼痛对标准护理治疗无效,是导致发病和痛苦的一个重要因素。近年来,针对SCI的动物研究和转化模型取得的进展,加深了我们对促进神经性疼痛的神经元兴奋性、胶质细胞失调和慢性炎症过程的理解。这些进展有助于推动对神经调节作为一种治疗方式的探索。在临床前和临床环境中,使用鞘内药物递送(IDD)和新型药物疗法来治疗慢性神经性疼痛受到了特别关注。在这篇基于证据的叙述性综述中,我们全面探讨了SCI后神经性疼痛发病机制的新证据、IDD作为一种治疗策略的证据基础,以及在有影响力的动物和临床研究中的新型药物。