Possible involvement of prolonging spinal µ‐opioid receptor desensitization in the development of antihyperalgesic tolerance to µ‐opioids under a neuropathic pain‐like state. (4th August 2011)

• Record Type: Journal Article
• Authors: Narita, Minoru; Imai, Satoshi; Nakamura, Atsushi; Ozeki, Ayumi; Asato, Megumi; Rahmadi, Mahardian; Sudo, Yuka; Hojo, Minoru; Uezono, Yasuhito; Devi, Lakshmi A.; Kuzumaki, Naoko; Suzuki, Tsutomu
• Is Part Of: Addiction biology. Volume 18:Number 4(2013:Jul.)
• Page Start: 614
• Page End: 622
• Publication Date: 2011-08-04
• Subjects: Substance abuse -- Periodicals; Substance abuse -- Physiological aspects -- Periodicals; Substance-Related Disorders -- periodicals; 616.86
• DOI: 10.1111/j.1369-1600.2011.00354.x
• Languages: English
• ISSNs: 1355-6215

Abstract

<abstract abstract-type="main" xml:lang="en"> <title>ABSTRACT</title> <p>In the present study, we investigated the possible development of tolerance to the antihyperalgesic effect of µ‐opioid receptor (MOR) agonists under a neuropathic pain‐like state. Repeated treatment with fentanyl, but not morphine or oxycodone, produced a rapid development of tolerance to its antihyperalgesic effect in mice with sciatic nerve ligation. Like the behavioral study, G‐protein activation induced by fentanyl was significantly reduced in membranes obtained from the spinal cord of nerve‐ligated mice with in vivo repeated injection of fentanyl. In β‐endorphin‐knockout mice with nerve ligation, developed tolerance to the antihyperalgesic effect of fentanyl was abolished, and reduced G‐protein activation by fentanyl after nerve ligation with fentanyl was reversed to the normal level. The present findings indicate that released β‐endorphin within the spinal cord may be implicated in the rapid development of tolerance to fentanyl under a neuropathic pain‐like state.</p> </abstract>