Pharmacology Update: Suzetrigine: A Novel NaV1.8 Sodium Channel Inhibitor for Acute Pain Management.

IF 1.4
Supriya Peshin, Claudia Villa Celi, Saima Rashid, Asti Rego, Steven J Baumrucker
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Abstract

Suzetrigine (formerly known as VX-548) is a novel sodium channel inhibitor that selectively targets NaV1.8, a key mediator in pain signal transmission, particularly in peripheral nociceptive neurons. This mechanism distinguishes suzetrigine from traditional opioid therapies, offering an effective alternative for acute pain management without the risks of addiction, sedation, or respiratory depression commonly associated with opioids. This literature review examines the pharmacology, mechanism of action, and clinical efficacy of suzetrigine, with an emphasis on its role in acute pain reduction, safety profile, and emerging clinical applications. Preclinical research on suzetrigine and earlier NaV1.8 inhibitors has demonstrated significant reductions in nociceptive behaviors in animal models of inflammatory and neuropathic pain, with minimal off-target effects on other sodium channels such as NaV1.7 and NaV1.9. Unlike opioids and nonsteroidal anti-inflammatory drugs (NSAIDs), suzetrigine acts by selectively inhibiting NaV1.8 channels, which play a specialized role in pain amplification, while sparing central nervous system pathways. In Phase 2 clinical trials involving patients undergoing bunionectomy and abdominoplasty, suzetrigine achieved significant reductions in postoperative pain compared to placebo and demonstrated analgesic efficacy comparable to hydrocodone/acetaminophen. This review highlights the advantages of suzetrigine over current pain management drugs, particularly its ability to relieve pain without side the unwanted side effects from opioids. Suzetrigine has been well-tolerated in both preclinical and clinical settings, with mild gastrointestinal symptoms reported as the most common adverse effect. Its selective mechanism makes suzetrigine a strong candidate for use in multimodal analgesic regimens, especially in postoperative care or among patients at risk for opioid misuse. In the context of the ongoing opioid crisis, suzetrigine represents a promising advancement in acute pain treatment. However, further research is needed to evaluate its long-term safety and efficacy, especially in chronic pain conditions and in combination with other analgesics. As its clinical use expands, suzetrigine may offer a critical tool for reducing opioid dependency across both acute and long-term pain management strategies.

药理学更新:suzetriine:一种用于急性疼痛管理的新型NaV1.8钠通道抑制剂。
Suzetrigine(原名VX-548)是一种新型钠通道抑制剂,可选择性靶向NaV1.8, NaV1.8是疼痛信号传递的关键介质,特别是外周伤害性神经元。这一机制将suzetriine与传统的阿片类药物疗法区分开来,为急性疼痛管理提供了一种有效的替代方案,而没有阿片类药物通常相关的成瘾、镇静或呼吸抑制风险。本文综述了舒三嗪的药理学、作用机制和临床疗效,重点介绍了舒三嗪在减轻急性疼痛方面的作用、安全性和临床应用。临床前研究表明,舒三嗪和早期的NaV1.8抑制剂可显著降低炎症性和神经性疼痛动物模型中的伤害性行为,对其他钠通道(如NaV1.7和NaV1.9)的脱靶作用最小。与阿片类药物和非甾体抗炎药(NSAIDs)不同,suzetriine通过选择性抑制NaV1.8通道起作用,而NaV1.8通道在疼痛放大中起特殊作用,同时保留中枢神经系统通路。在涉及拇囊炎切除术和腹部成形术患者的2期临床试验中,与安慰剂相比,suzetriine显著减少了术后疼痛,并证明了与氢可酮/对乙酰氨基酚相当的镇痛效果。这篇综述强调了suzetriine相对于目前的疼痛管理药物的优势,特别是它在没有阿片类药物副作用的情况下减轻疼痛的能力。suzetriine在临床前和临床环境中均具有良好的耐受性,最常见的不良反应是轻度胃肠道症状。其选择性机制使suzetriine成为多模式镇痛方案的有力候选方案,特别是在术后护理或有阿片类药物滥用风险的患者中。在持续的阿片类药物危机的背景下,suzetrigine代表了急性疼痛治疗的一个有希望的进展。然而,需要进一步的研究来评估其长期安全性和有效性,特别是在慢性疼痛条件下和与其他镇痛药合用。随着临床应用的扩大,suzetriine可能会在急性和长期疼痛管理策略中提供减少阿片类药物依赖的关键工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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