Xiangsunze Zeng,Rosa I Martinez-Garcia,Shamsuddin A Bhuiyan,Keunjung Heo,Natalie MacKinnon-Booth,Elke Bentley,Emily Shea,Kangling Wu,Omer Barkai,Bruna Lenfers Turnes,Selwyn S Jayakar,Barbara Gomez-Eslava,Mustafa Q Hameed,Celine Santiago,Karina Lezgiyeva,Emmanuella Osei-Asante,Ivan Furfaro,Alexander Rotenberg,Benjamin R Johnston,Brian J Wainger,William Renthal,Stéphanie P Lacour,David D Ginty,Clifford J Woolf
bioRxiv the preprint server for biology(2025)
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摘要
Spontaneous pain is a very common but poorly understood consequence of peripheral nerve injury. We developed a system for measuring spontaneous pain-related behaviors in mice over months, which revealed that limb flicks-emerging predominantly 2 months post-injury-reflect spontaneous pain, and that neuromas are the drivers of this component of neuropathic pain. In vivo dorsal root ganglion imaging showed that small-diameter sensory neurons are the source of spontaneous ectopic neuroma activity and are different from the intact neurons that drive stimulus-evoked pain. Cell-specific optogenetic stimulation studies identified that injured SSTR2 + sensory axons in neuromas are the triggers of spontaneous limb flicks/neuropathic pain. These findings reveal the mechanisms of spontaneous neuropathic pain and open new therapeutic opportunities.