Suzetrigine:首个获批用于治疗中度至重度急性疼痛的Nav1.8抑制剂。

IF 1.5 Q3 PHARMACOLOGY & PHARMACY
Drug Discoveries and Therapeutics Pub Date : 2025-03-06 Epub Date: 2025-02-27 DOI:10.5582/ddt.2025.01010
Shasha Hu, Dong Lyu, Jianjun Gao
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引用次数: 0

摘要

阿片类药物通常用于治疗中度至重度疼痛,但其使用与依赖性和其他不良反应有关。几十年来,用于治疗中度至重度疼痛的安全有效的非成瘾性替代品的开发进展有限。2025年1月30日,美国食品和药物管理局批准首个Nav1.8抑制剂suzetrigine用于治疗中至重度急性疼痛。Nav1.8是一种电压门控钠通道,在负责传递疼痛信号的外周伤害性神经元中选择性表达。suzetriine通过高度选择性抑制Nav1.8通道,有效缓解疼痛。与阿片类药物不同,这种药物不会在大脑中引起欣快感或兴奋,从而消除了对成瘾的担忧。suzetriine提供了一种新的治疗选择和多模式镇痛的潜在组合,有望改变急性疼痛管理和建立新的治疗标准。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Suzetrigine: The first Nav1.8 inhibitor approved for the treatment of moderate to severe acute pain.

Opioids are commonly prescribed for the management of moderate to severe pain, but their use is associated with dependency and other adverse effects. For decades, the development of safe and effective non-addictive alternatives for treating moderate to severe pain has seen limited progress. On January 30, 2025, the U.S. Food and Drug Administration approved suzetrigine, the first Nav1.8 inhibitor, for the treatment of moderate to severe acute pain. Nav1.8 is a voltage-gated sodium channel that is selectively expressed in peripheral nociceptive neurons, which are responsible for transmitting pain signals. By highly selectively inhibiting the Nav1.8 channel, suzetrigine can effectively alleviate pain. Unlike opioids, this drug does not induce euphoria or excitement in the brain, thereby eliminating concerns about addiction. Suzetrigine offers a novel therapeutic option and a potential combination for multimodal analgesia, with the promise of transforming acute pain management and establishing new treatment standards.

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来源期刊
Drug Discoveries and Therapeutics
Drug Discoveries and Therapeutics PHARMACOLOGY & PHARMACY-
CiteScore
3.20
自引率
3.20%
发文量
51
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