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.
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Authors | Hisayoshi Tamai, Shigehito Sawamura, Kenji Takeda, Ryo Orii, Kazuo Hanaoka |
Journal | European journal of pharmacology
(Eur J Pharmacol)
Vol. 510
Issue 3
Pg. 223-8
(Mar 14 2005)
ISSN: 0014-2999 [Print] Netherlands |
PMID | 15763246
(Publication Type: Journal Article)
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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
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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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