Stage‐dependent C‐reflex, pain‐like behavior and opioid analgesia during the induction of chronic arthritis in rats. (21st August 2014)

• Record Type: Journal Article
• Authors: Alvarez, Pedro; Hernández, Alejandro; Constandil, Luis; Infante, Claudio; Pelissier, Teresa
• Is Part Of: European journal of neuroscience. Volume 40:Number 8(2014:Oct.)
• Page Start: 3264
• Page End: 3272
• Publication Date: 2014-08-21
• Subjects: Nervous system -- Periodicals; 612.8
• DOI: 10.1111/ejn.12685
• Languages: English
• ISSNs: 0953-816X

Abstract

<abstract abstract-type="main" id="ejn12685-abs-0001"> <title>Abstract</title> <p>Chronic arthritis (CA) is a common clinical entity associated with persistent pain and limited response to opioid analgesic therapy. However, it is unknown whether these features of CA change depending on its stage of evolution. To address this, in a well‐established animal model of CA we studied the time course of electromyographic responses to electrical stimulation of C fibers (C‐reflex), pain‐like behavior as a response to mechanical nociceptive stimulation, and the inhibition of both responses by a prototypic opioid analgesic, morphine. To induce CA, rats received a single injection of complete Freund's adjuvant into the ankle joint and the C‐reflex responses to electrical stimuli or the nociceptive response to paw pressure test were studied 2, 4 or 6 weeks later. The C‐reflexes evoked by threshold and supra‐threshold electrical stimulation exhibited progressive increases together with enhancement of the nociceptive behavior to mechanical stimulation during induction of monoarthritis. Notably, while systemic morphine produced antinociceptive effects upon both experimental approaches, the effects were markedly reduced during the early stages of CA but enhanced at later stages. These data indicate that C‐reflex and pain‐like responses evolve in parallel, and are inhibited by morphine in a stage‐dependent manner through the induction of CA. The present results may contribute to explain the enhanced pain response and variable analgesic efficacy of opioids that characterize arthritic pain in humans.</p> </abstract>