Opioidergic and adrenergic modulation of formalin-evoked spinal c-fos mRNAexpression and nocifensive behavior in the rat

Citation
S. Sawamura et al., Opioidergic and adrenergic modulation of formalin-evoked spinal c-fos mRNAexpression and nocifensive behavior in the rat, EUR J PHARM, 379(2-3), 1999, pp. 141-149
Citations number
57
Categorie Soggetti
Pharmacology & Toxicology
Journal title
EUROPEAN JOURNAL OF PHARMACOLOGY
ISSN journal
00142999 → ACNP
Volume
379
Issue
2-3
Year of publication
1999
Pages
141 - 149
Database
ISI
SICI code
0014-2999(19990827)379:2-3<141:OAAMOF>2.0.ZU;2-B
Abstract
Fos protein expression has been used to reflect neuronal activation in pain processing pathways although analgesics may uncouple behavioral and Fos re sponses. We determine whether formalin-induced spinal c-fos mRNA expression (Northern blotting) correlates with nocifensive behavior following pretrea tment with morphine, the alpha(2)-adrenoceptor agonist dexmedetomidine. or their respective antagonists naloxone and atipamezole. Both opiate and alph a(2)-adrenoceptor agonists reduced formalin-induced c-fos gene transcriptio n and nocifensive behavior via their cognate receptors. Unexpectedly, block ade of either the opiate or alpha(2)-adrenergic receptors, alone, caused an increase in formalin-evoked c-fos mRNA: while blocking the opiate receptor had no effect on formalin-induced behavior, alpha(2)-adrenoceptor block ha d an analgesic effect, indicating discordance between c-fos message transcr iption and nocifensive behavior. We concluded that the formalin-induced spi nal c-fos signal was a poor predictor of the behavioral response to pharmac ological manipulation of pain processing pathways. (C) 1999 Elsevier Scienc e B.V. All rights reserved.