Abstract | BACKGROUND: METHODS: Twenty-four young male Sprague-Dawley rats received L5 single spinal-nerve injury. Nerve-injured rats (6 per group) received repeated intraperitoneal administrations of meloxicam (1, 2, or 4 mg/kg) or vehicle 0, 12, 24, and 36 hours after nerve injury. Tactile allodynia was quantified for 4 weeks by use of von Frey filaments. RESULTS: In animals given 2 mg/kg and 4 mg/kg, hind-paw withdrawal thresholds 4 weeks after nerve injury were significantly higher compared with those of the vehicle-treated animals. The area under the time-effect curve from preinjury to 4 weeks after nerve injury values were significantly higher in animals treated with 4 mg/kg of meloxicam compared with animals treated with vehicle. CONCLUSION: Systemic administration of 2 mg/kg and 4 mg/kg of meloxicam at an early stage after nerve injury attenuated the development of tactile allodynia. These results suggest that COX-2 may be at least in part involved in the development of tactile allodynia in an L5 single spinal-nerve injury model.
|
Authors | Masahiro Takahashi, Masahiko Kawaguchi, Keiji Shimada, Toshikatsu Nakashima, Hitoshi Furuya |
Journal | Regional anesthesia and pain medicine
(Reg Anesth Pain Med)
2005 Jul-Aug
Vol. 30
Issue 4
Pg. 351-5
ISSN: 1098-7339 [Print] England |
PMID | 16032587
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
|
Chemical References |
- Analgesics, Non-Narcotic
- Cyclooxygenase 2 Inhibitors
- Cyclooxygenase Inhibitors
- Thiazines
- Thiazoles
- Cyclooxygenase 2
- Prostaglandin-Endoperoxide Synthases
- Meloxicam
|
Topics |
- Analgesics, Non-Narcotic
(pharmacology)
- Animals
- Cyclooxygenase 2
- Cyclooxygenase 2 Inhibitors
- Cyclooxygenase Inhibitors
(pharmacology)
- Male
- Meloxicam
- Pain
(prevention & control)
- Prostaglandin-Endoperoxide Synthases
(physiology)
- Rats
- Rats, Sprague-Dawley
- Spinal Nerves
(injuries)
- Thiazines
(pharmacology)
- Thiazoles
(pharmacology)
|