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Anti-allodynic and anti-hyperalgesic effects of nociceptin receptor antagonist, JTC-801, in rats after spinal nerve injury and inflammation.

Abstract
The effects of nociceptin/orphanin FQ (N/OFQ) peptide receptor antagonist JTC-801 on allodynia and hyperalgesia were examined in rats in order to explore the involvement of N/OFQ system in these pathological pain states. Tactile allodynia induced by L5/L6 spinal nerve ligation was reversed by both systemic (3-30 mg/kg) and spinal (22.5 and 45 pg) JTC-801 in a dose-dependent manner. Concerning hyperalgesia induced by formalin injection into the hindpaw, JTC-801 dose-dependently suppressed the second phase, but not the first phase, of the licking behavior. Furthermore, systemic JTC-801 reduced Fos-like immunoreactivity in the dorsal horn of the spinal cord (laminae I/II). In conclusion, N/OFQ receptor antagonist JTC-801 exerted anti-allodynic and anti-hyperalgesic effects in rats, suggesting that N/OFQ system might be involved in the modulation of neuropathic pain and inflammatory hyperalgesia.
AuthorsHisayoshi Tamai, Shigehito Sawamura, Kenji Takeda, Ryo Orii, Kazuo Hanaoka
JournalEuropean journal of pharmacology (Eur J Pharmacol) Vol. 510 Issue 3 Pg. 223-8 (Mar 14 2005) ISSN: 0014-2999 [Print] Netherlands
PMID15763246 (Publication Type: Journal Article)
Chemical References
  • Aminoquinolines
  • Benzamides
  • N-(4-amino-2-methylquinolin-6-yl)-2-(4-ethylphenoxymethyl)benzamide
  • Narcotic Antagonists
  • Proto-Oncogene Proteins c-fos
  • Receptors, Opioid
  • Nociceptin Receptor
  • Oprl protein, rat
Topics
  • Aminoquinolines (pharmacology)
  • Animals
  • Benzamides (pharmacology)
  • Hyperalgesia (physiopathology, prevention & control)
  • Hyperesthesia (physiopathology, prevention & control)
  • Male
  • Narcotic Antagonists
  • Neuritis (physiopathology, prevention & control)
  • Pain Measurement
  • Proto-Oncogene Proteins c-fos (metabolism)
  • Rats
  • Rats, Sprague-Dawley
  • Receptors, Opioid
  • Spinal Nerves (drug effects, injuries, physiopathology)
  • Touch
  • Nociceptin Receptor

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