Suzetrigine: The first Nav1.8 inhibitor approved for the treatment of moderate to severe acute pain

被引:0
|
作者
Hu, Shasha [1 ]
Lyu, Dong [2 ]
Gao, Jianjun [3 ]
机构
[1] Qingdao Univ, Dept Pathol, Affiliated Hosp, Qingdao, Shandong, Peoples R China
[2] Qingdao Univ, Weihai Cent Hosp, Dept Burn & Plast Surg, Weihai, Shandong, Peoples R China
[3] Qingdao Univ, Sch Pharm, Dept Pharmacol, Qingdao, Shandong, Peoples R China
关键词
Opioids; Nav1.8; pain; postoperative; painful diabetic peripheral neuropathy (DPN); painful lumbosacral radiculopathy (LSR);
D O I
10.5582/ddt.2025.01010
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
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 nonaddictive 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.
引用
收藏
页数:3
相关论文
共 50 条
  • [41] Optogenetic Inhibition of Nav1.8 Expressing Corneal Afferents Reduces Persistent Dry Eye Pain
    Mecum, Neal E.
    Russell, Rachel
    Lee, Jun
    Sullivan, Cara
    Meng, Ian D.
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2021, 62 (14)
  • [42] Melatonin attenuated chronic visceral pain by reducing Nav1.8 expression and nociceptive neuronal sensitization
    Lv, Meng-Dan
    Wei, Ying-Xue
    Chen, Jian-Peng
    Cao, Ming-Yao
    Wang, Qian-Liang
    Hu, Shufen
    MOLECULAR PAIN, 2023, 19
  • [43] Inhibition of neuropathic pain by decreased expression of the tetrodotoxin-resistant sodium channel, NaV1.8
    Lai, J
    Gold, MS
    Kim, CS
    Bian, D
    Ossipov, MH
    Hunter, JC
    Porreca, F
    PAIN, 2002, 95 (1-2) : 143 - 152
  • [44] THE DISCOVERY OF HIGHLY SELECTIVE NaV1.8 MODULATORS WITH GOOD PHARMACOKINETIC PROPERTIES FOR CHRONIC MIXED PAIN
    Kemp, Mark
    DRUGS OF THE FUTURE, 2009, 34 : 16 - 17
  • [45] Pain behavior in SCN9A (Nav1.7) and SCN10A (Nav1.8) mutant rodent models
    Xue, Yaping
    Chidiac, Celeste
    Herault, Yann
    Gaveriaux-Ruff, Claire
    NEUROSCIENCE LETTERS, 2021, 753
  • [46] Correlation of Nav1.8 and Nav1.9 sodium channel expression with neuropathic pain in human subjects with lingual nerve neuromas
    Bird, Emma V.
    Christmas, Claire R.
    Loescher, Alison R.
    Smith, Keith G.
    Robinson, Peter P.
    Black, Joel A.
    Waxman, Stephen G.
    Boissonade, Fiona M.
    MOLECULAR PAIN, 2013, 9
  • [47] Lidocaine reduces pain behaviors by inhibiting the expression of Nav1.7 and Nav1.8 and diminishing sympathetic sprouting in SNI rats
    Li, Xiaoxiao
    Chen, Han
    Zhu, Yujing
    Li, Yanyan
    Zhang, Tan
    Tang, Jun
    MOLECULAR PAIN, 2022, 18
  • [48] Histamine Modulation of Acute Nociception Involves Regulation of Nav1.8 in Primary Afferent Neurons in Mice
    Yu, Jie
    Fang, Qi
    Lou, Guo-Dong
    Shou, Wen-Ting
    Yue, Jia-Xing
    Tang, Ying-Ying
    Hou, Wei-Wei
    Xu, Tian-Le
    Ohtsu, Hiroshi
    Zhang, Shi-Hong
    Chen, Zhong
    CNS NEUROSCIENCE & THERAPEUTICS, 2013, 19 (09) : 649 - 658
  • [49] Histamine modulation of acute nociception involves regulation of Nav1.8 in primary afferent neurons in mice
    于捷
    Hiroshi Ohtsu
    中国药理学与毒理学杂志, 2012, 26 (03) : 432 - 433
  • [50] Roles of ASIC3, TRPV1, and NaV1.8 in the transition from acute to chronic pain in a mouse model of fibromyalgia
    Chen, Wei-Nan
    Lee, Cheng-Han
    Lin, Shing-Hong
    Wong, Chia-Wen
    Sun, Wei-Hsin
    Wood, John N.
    Chen, Chih-Cheng
    MOLECULAR PAIN, 2014, 10