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疼痛管理中的新型非阿片类镇痛药。

Novel non-opioid analgesics in pain management.

作者信息

Pulskamp Tariq G, Johnson Lucy M, Berlau Daniel J

机构信息

School of Pharmacy, Regis University, Denver, CO, USA.

出版信息

Pain Manag. 2024 Dec;14(12):641-651. doi: 10.1080/17581869.2024.2442292. Epub 2024 Dec 18.

DOI:10.1080/17581869.2024.2442292
PMID:39692452
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11702995/
Abstract

Effective pain management has long been hindered by the limitations and risks associated with opioid analgesics, necessitating the exploration of novel, non-opioid alternatives. A comprehensive literature search was conducted using PubMed and Google Scholar during October and November 2024 to identify studies on emerging non-opioid pain management therapeutics. This review evaluates three promising classes of mechanism-specific therapeutics: nerve growth factor (NGF) monoclonal antibodies, transient receptor potential vanilloid 1 (TRPV1) antagonists, and selective sodium channel blockers. By targeting distinct pathways involved in pain sensation, these therapies aim to provide relief for various pain types, including chronic, inflammatory, and neuropathic pain, with potentially fewer side effects. Through a detailed analysis of their mechanisms of action and current evidence, this review highlights the clinical potential of each class, addressing both their efficacy and safety challenges. Ultimately, these emerging therapies represent significant advancements in non-opioid pain management, with the potential to reshape standard approaches to patient care.

摘要

长期以来,阿片类镇痛药的局限性和风险一直阻碍着有效的疼痛管理,因此有必要探索新型的非阿片类替代药物。2024年10月至11月期间,利用PubMed和谷歌学术进行了全面的文献检索,以确定关于新兴非阿片类疼痛管理疗法的研究。本综述评估了三类有前景的作用机制特异性疗法:神经生长因子(NGF)单克隆抗体、瞬时受体电位香草酸亚型1(TRPV1)拮抗剂和选择性钠通道阻滞剂。通过针对疼痛感觉中涉及的不同途径,这些疗法旨在缓解各种类型的疼痛,包括慢性疼痛、炎症性疼痛和神经性疼痛,且副作用可能更少。通过对其作用机制和现有证据的详细分析,本综述突出了每类疗法的临床潜力,同时探讨了它们在疗效和安全性方面面临的挑战。最终,这些新兴疗法代表了非阿片类疼痛管理的重大进展,有可能重塑患者护理的标准方法。

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本文引用的文献

1
Discovery of Dual TRPA1 and TRPV1 Antagonists as Novel Therapeutic Agents for Pain.发现双重TRPA1和TRPV1拮抗剂作为新型疼痛治疗药物
Pharmaceuticals (Basel). 2024 Sep 13;17(9):1209. doi: 10.3390/ph17091209.
2
State-Dependent Inhibition of Nav1.8 Sodium Channels by VX-150 and VX-548.状态依赖抑制 Nav1.8 钠离子通道 VX-150 和 VX-548。
Mol Pharmacol. 2024 Nov 18;106(6):298-308. doi: 10.1124/molpharm.124.000944.
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Human heat sensation: A randomized crossover trial.人体热感觉:一项随机交叉试验。
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Nanomedicine and voltage-gated sodium channel blockers in pain management: a game changer or a lost cause?纳米医学与电压门控钠离子通道阻滞剂在疼痛管理中的应用:改变游戏规则还是错失良机?
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N Engl J Med. 2023 Aug 3;389(5):393-405. doi: 10.1056/NEJMoa2209870.
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A Randomized Placebo-Controlled Trial of the Anti-Nerve Growth Factor Antibody Tanezumab in Subjects With Cancer Pain Due to Bone Metastasis.一项抗神经生长因子抗体替扎尼珠单抗治疗骨转移癌痛受试者的随机安慰剂对照试验。
Oncologist. 2023 Dec 11;28(12):e1268-e1278. doi: 10.1093/oncolo/oyad188.
8
Topical Ocular TRPV1 Antagonist SAF312 (Libvatrep) for Postoperative Pain After Photorefractive Keratectomy.局部眼部 TRPV1 拮抗剂 SAF312(利伐曲普坦)治疗屈光性角膜切削术后疼痛。
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Computational design of peptides to target Na1.7 channel with high potency and selectivity for the treatment of pain.针对 Na1.7 通道进行高活性和高选择性的肽类药物设计,用于疼痛治疗。
Elife. 2022 Dec 28;11:e81727. doi: 10.7554/eLife.81727.
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A novel anti-NGF PEGylated Fab' provides analgesia with lower risk of adverse effects.一种新型抗神经生长因子聚乙二醇化 Fab' 提供镇痛作用,不良反应风险较低。
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