The antinociceptive effect of intrathecal administration of epibatidine with clonidine or neostigmine in the formalin test in rats

Citation
At. Hama et al., The antinociceptive effect of intrathecal administration of epibatidine with clonidine or neostigmine in the formalin test in rats, PAIN, 91(1-2), 2001, pp. 131-138
Citations number
47
Categorie Soggetti
Neurology,"Neurosciences & Behavoir
Journal title
PAIN
ISSN journal
03043959 → ACNP
Volume
91
Issue
1-2
Year of publication
2001
Pages
131 - 138
Database
ISI
SICI code
0304-3959(200103)91:1-2<131:TAEOIA>2.0.ZU;2-F
Abstract
The analgesic effect of intrathecal injection of epibatidine, clonidine and neostigmine, compounds that elevate ACh, was examined in the formalin test , a model of post-injury central sensitization in the rat. The compounds we re injected alone and in combination. Intrathecal injection of epibatidine alone did not alter pain behaviors, compared to vehicle-treated rats. Intra thecal injection of clonidine dose-dependently reduced tonic pain behaviors (ED50 +/- 95% confidence limits = 6.7 +/- 4.8 mug). The combination of clo nidine and epibatidine (C:E), in the ratio of 26:1, dose-dependently reduce d tonic pain behaviors; and the ED50 of C:E was 1.1 +/- 0.98 mug a signific ant 6-fold leftward shift of the dose response curve, compared with clonidi ne alone. The antinociceptive effect of C:E (26:1) was attenuated by pre-tr eatment with the nAChR antagonist mecamylamine. Neostigmine dose-dependentl y reduced tonic pain behaviors (ED50 = 1.5 +/- 1.3 mug). The combination of neostigmine and epibatidine, in a ratio of 8:1, significantly shifted the dose response curve 4-fold to the left (ED50 = 0-4 +/- 0.3 mug). The effect is mediated in part by the activation of the nAChR and possibly by the enh anced release of ACh. These data demonstrate significant enhancement of the antinociceptive effects of spinally delivered analgesics by a nAChR agonis t, suggesting that this class of compounds may have utility as adjuvants wh en combined with conventional therapeutics. (C) 2001 International Associat ion for the Study of Pain. Published by Elsevier Science B.V. All rights re served.