Korean J Anesthesiol.  2007 Jan;52(1):81-90. 10.4097/kjae.2007.52.1.81.

Effect of Intrathecal COX Inhibitors on Inflammatory Pain and c-Fos Expression in Central Nervous System Induced by Formalin Injection in Rat

Affiliations
  • 1Department of Aneathesiology and Pain Medicine, College of Medicine, Korea University, Seoul, Korea. iloklee@korea.ac.kr

Abstract

BACKGROUND
Prostaglandins (PGs) play important roles in the transmission of nociceptive information in the spinal cord. PGs are produced by cyclooxygenase (COX). Two forms of COX have been identified: COX-1 and COX-2. c-Fos is a marker of neuronal activity related to the stimulation of primary sensory neuron. We investigated the effect of intrathecal non-selective COX inhibitor, selective COX-1 or COX-2 inhibitors on the inflammatory pain and c-Fos expression in the brain.
METHODS
A PE (polyethylene) intrathecal catheter was installed in male Sprague-Dawley rats (250-300 g). Control, nonselective COX inhibitor, COX-1 inhibitor, and COX-2 inhibitor groups (n = 8, each) received intrathecal dimethylsulfoxide (DMSO) solution, ketorolac 50microgram, SC-560 50microgram, or celecoxib 50microgram respectively 7 min before formalin injection. For formalin test, rats received 50microliter of 5% formalin in the right hindpaw subcutaneously. Pain-related behavior was quantified by counting the incidence of flinching for 60 minutes. c-Fos expression in the thalamus, hypothalamus, and amygdala was examined by immunohistochemistry.
RESULTS
Nonselective COX inhibitor and COX-2 inhibitor groups showed less frequent phase 2 flinching than the control (P < 0.05). But there was no significant differences in the expression of FLI in the thalamus, hypothalamus, and amygdala between control and experimental groups. And the expression of FLI was not correlated with flinching behavior.
CONCLUSIONS
These result represented that COX-2 would play important roles in the transmission of pain induced by formalin test and that FLI in thalamus, hypothalamus, and amygdala could not be a good parameter for evaluating central sensitization.

Keyword

brain; cyclooxygenase inhibitors; fos; gene; injection; spinal

MeSH Terms

Amygdala
Animals
Brain
Catheters
Central Nervous System Sensitization
Central Nervous System*
Cyclooxygenase 2 Inhibitors
Cyclooxygenase Inhibitors
Dimethyl Sulfoxide
Formaldehyde*
Humans
Hypothalamus
Immunohistochemistry
Incidence
Ketorolac
Male
Neurons
Pain Measurement
Prostaglandin-Endoperoxide Synthases
Prostaglandins
Rats*
Rats, Sprague-Dawley
Sensory Receptor Cells
Spinal Cord
Thalamus
Celecoxib
Cyclooxygenase 2 Inhibitors
Cyclooxygenase Inhibitors
Dimethyl Sulfoxide
Formaldehyde
Ketorolac
Prostaglandin-Endoperoxide Synthases
Prostaglandins
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