{"title":"Spinal nociceptive hypersensitivity induced by intramuscular capsaicin in rats subjected to multiple continuous stress.","authors":"Rikuo Yamamoto, Koji Wakatsuki, Masaya Yasui, Hiroki Ota, Kazue Mizumura, Toru Taguchi","doi":"10.1016/j.neures.2025.02.009","DOIUrl":null,"url":null,"abstract":"<p><p>Persistent physical and psychological stress is highly relevant to the development of chronic muscle pain; however, the neural mechanisms underlying stress-induced hyperalgesia remain largely unknown. This study aimed to elucidate the peripheral and spinal mechanisms of stress-induced muscle hyperalgesia using a rat model developed under multiple continuous stress (MCS) by keeping rats in a cage filled with shallow water (1.5cm in depth) for 5 or 6 days. In the MCS rats, intramuscular injection of capsaicin (300μM, 50μL), which activates TRPV1-positive muscular C-fiber nociceptors, increased pain-related facial expressions scored using a rat grimace scale. Intramuscular capsaicin injections induced significant c-Fos expression throughout the ipsilateral spinal dorsal horn (laminae I-VI) at segments L3-L5 in rats exposed to MCS, when compared to naïve control rats. Increased c-Fos expression was also observed on the contralateral side in the MCS group. Single-fiber electrophysiological recordings using ex vivo muscle-nerve preparations revealed that neither the general characteristics nor the responsiveness of muscular C-fibers to noxious stimuli were altered in the MCS group. These results indicate that spinal nociceptive hypersensitivity is associated with muscle pain induced by MCS. However, it is unlikely to be mediated by altered responses to muscular C-fiber nociceptors.</p>","PeriodicalId":19146,"journal":{"name":"Neuroscience Research","volume":" ","pages":""},"PeriodicalIF":2.4000,"publicationDate":"2025-03-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Neuroscience Research","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1016/j.neures.2025.02.009","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"NEUROSCIENCES","Score":null,"Total":0}
引用次数: 0
Abstract
Persistent physical and psychological stress is highly relevant to the development of chronic muscle pain; however, the neural mechanisms underlying stress-induced hyperalgesia remain largely unknown. This study aimed to elucidate the peripheral and spinal mechanisms of stress-induced muscle hyperalgesia using a rat model developed under multiple continuous stress (MCS) by keeping rats in a cage filled with shallow water (1.5cm in depth) for 5 or 6 days. In the MCS rats, intramuscular injection of capsaicin (300μM, 50μL), which activates TRPV1-positive muscular C-fiber nociceptors, increased pain-related facial expressions scored using a rat grimace scale. Intramuscular capsaicin injections induced significant c-Fos expression throughout the ipsilateral spinal dorsal horn (laminae I-VI) at segments L3-L5 in rats exposed to MCS, when compared to naïve control rats. Increased c-Fos expression was also observed on the contralateral side in the MCS group. Single-fiber electrophysiological recordings using ex vivo muscle-nerve preparations revealed that neither the general characteristics nor the responsiveness of muscular C-fibers to noxious stimuli were altered in the MCS group. These results indicate that spinal nociceptive hypersensitivity is associated with muscle pain induced by MCS. However, it is unlikely to be mediated by altered responses to muscular C-fiber nociceptors.
期刊介绍:
The international journal publishing original full-length research articles, short communications, technical notes, and reviews on all aspects of neuroscience
Neuroscience Research is an international journal for high quality articles in all branches of neuroscience, from the molecular to the behavioral levels. The journal is published in collaboration with the Japan Neuroscience Society and is open to all contributors in the world.