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外周N-甲基-D-天冬氨酸(NMDA)受体在瘙痒和疼痛中的作用:一项叙述性综述

The Role of Peripheral N-Methyl-D-Asparate (NMDA) Receptors in Itch and Pain: A Narrative Review.

作者信息

Tanaka Ryusuke, Lo Vecchio Silvia, Aliotta Giulia Erica, Arendt-Nielsen Lars

机构信息

Department of Health Science and Technology, Center for Neuroplasticity and Pain (CNAP), Aalborg University, Aalborg, Denmark.

Department of Anesthesiology and Resuscitology, Shinshu University School of Medicine, Matsumoto, Japan.

出版信息

Eur J Pain. 2025 Aug;29(7):e70082. doi: 10.1002/ejp.70082.

Abstract

BACKGROUND AND OBJECTIVE

NMDA receptors, predominantly located in the central nervous system and known for their roles in synaptic plasticity and central sensitisation of pain and itch, are also expressed in peripheral sensory neurons. Emerging evidence suggests that peripheral NMDA receptors contribute to pathological pain and potentially itch, identifying them as promising therapeutic targets. The aim of this review is to explore the role of peripheral NMDA receptors in pain and itch and to summarise the effectiveness of topical NMDA antagonists in managing these sensations.

DATABASES AND DATA TREATMENT

This review was conducted through a systematic search of the PubMed database using MeSH terms and keywords related to 'peripheral NMDA receptors', 'pain', 'itch' and 'topical ketamine'. Additional references were included based on expert knowledge and reference tracking. Only English-language articles were considered.

RESULTS

Animal studies demonstrate that peripheral NMDA receptors are involved in inflammatory and certain neuropathic pain models, with antagonists showing analgesic effects. Limited studies also suggest their role in non-histaminergic itch through glutamate signalling. In humans, topical ketamine has shown mixed results for pain relief, and preliminary clinical reports suggest potential antipruritic effects. However, controlled clinical trials, particularly for itch, are lacking.

CONCLUSION

Peripheral NMDA receptors are involved in the transmission and sensitisation of both pain and itch, especially under pathological conditions. While topical ketamine may offer therapeutic benefits, particularly for non-histaminergic itch and neuropathic pain, further clinical research is necessary to confirm its efficacy, safety and optimal use.

SIGNIFICANCE STATEMENT

This review highlights the underexplored role of peripheral NMDA receptors in itch, especially non-histaminergic pathways, and synthesises emerging evidence for their therapeutic potential. By comparing pain and itch mechanisms, it suggests that topical ketamine could serve as novel treatments for refractory itch and localised pain, warranting further clinical investigation.

摘要

背景与目的

N-甲基-D-天冬氨酸(NMDA)受体主要位于中枢神经系统,以其在突触可塑性以及疼痛和瘙痒的中枢敏化中的作用而闻名,同时也在外周感觉神经元中表达。新出现的证据表明,外周NMDA受体促成病理性疼痛,并可能与瘙痒有关,这使其成为有前景的治疗靶点。本综述的目的是探讨外周NMDA受体在疼痛和瘙痒中的作用,并总结局部应用NMDA拮抗剂在处理这些感觉方面的有效性。

数据库与数据处理

本综述通过使用与“外周NMDA受体”、“疼痛”、“瘙痒”和“局部应用氯胺酮”相关的医学主题词(MeSH)和关键词,对PubMed数据库进行系统检索。基于专家知识和参考文献追踪纳入了其他参考文献。仅考虑英文文章。

结果

动物研究表明,外周NMDA受体参与炎症性和某些神经性疼痛模型,拮抗剂显示出镇痛作用。有限的研究还表明它们通过谷氨酸信号传导在非组胺能性瘙痒中发挥作用。在人类中,局部应用氯胺酮在缓解疼痛方面结果不一,初步临床报告表明其可能有止痒作用。然而,缺乏对照临床试验,尤其是针对瘙痒的试验。

结论

外周NMDA受体参与疼痛和瘙痒的传递与敏化,尤其是在病理条件下。虽然局部应用氯胺酮可能具有治疗益处,特别是对于非组胺能性瘙痒和神经性疼痛,但需要进一步的临床研究来确认其疗效、安全性和最佳用法。

意义声明

本综述强调了外周NMDA受体在瘙痒(尤其是非组胺能途径)中未被充分探索的作用,并综合了关于其治疗潜力的新证据。通过比较疼痛和瘙痒机制,提示局部应用氯胺酮可作为难治性瘙痒和局部疼痛的新型治疗方法,值得进一步临床研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee74/12279002/b1fb622743ef/EJP-29-0-g001.jpg

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