Targeting Na(v)1.8 with the nonopioid antagonist suzetrigine for analgesia: cause for optimism?

使用非阿片类拮抗剂苏泽三嗪靶向Na(v)1.8进行镇痛:前景乐观吗?

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Abstract

The opioid crisis has prompted an urgent search for nonopioid analgesics for both acute and chronic pain. Among these, sodium channel antagonists, particularly those targeting Na(v)1.7 and Na(v)1.8, have emerged as potential pain management solutions. Recent large trials have shown some efficacy of the new Na(v)1.8 allosteric inhibitor suzetrigine in acute postoperative pain, and ongoing studies are investigating its potential for painful diabetic neuropathy. If efficacy is confirmed, this type of drug might fill a significant gap in the treatment of acute and chronic pain, offering a safer alternative to opioids and marking the advent of a new class of nonopioid analgesics.

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