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Gabapentin and Pregabalin Inhibit the Itch-Associated Response Induced by the Repeated Application of Oxazolone in Mice

Authors :
Yukihito Tsukumo
Yuichi Matsumoto
Hiroko Miura
Hiroshi Yano
Haruhiko Manabe
Source :
Journal of Pharmacological Sciences, Vol 115, Iss 1, Pp 27-35 (2011)
Publication Year :
2011
Publisher :
Elsevier, 2011.

Abstract

We investigated the effects of gabapentin and pregabalin on the itch-associated response in a mouse model of chronic dermatitis induced by the repeated application of 4-ethoxymethylene-2-phenyl-2-oxazolin-5-one (oxazolone). Challenging the mice with oxazolone-induced chronic dermatitis with the oxazolone evoked severe and transient scratching behavior until 1 h after the application of oxazolone. Thereafter, a more mild and continuous scratching behavior was also observed for at least 8 h. Both severe and continuous scratching behaviors were suppressed by systemic injection of gabapentin and pregabalin. This effect of these compounds was correlated with its affinity for the α2δ subunit of voltage-gated Ca2+ channels. Intrathecal injection, but not peripheral treatment, with gabapentin inhibited the scratching behavior in this model. Gabapentin failed to suppress the scratching behavior induced by the intradermal injection of compound 48/80 in normal mice. The expression of the α2δ-1 subunit in dorsal root ganglion (DRG) from mice following repeated application of oxazolone was significantly higher than that from normal mice. These results suggest that gabapentin and pregabalin show an anti-pruritic activity through α2δ-subunit binding, and the up-regulation of the α2δ-1 subunit in DRG may therefore play an important role in its anti-pruritic activity. Keywords:: gabapentin, pregabalin, pruritus, α2δ-1 subunit, oxazolone

Subjects

Subjects :
Therapeutics. Pharmacology
RM1-950

Details

Language :
English
ISSN :
13478613
Volume :
115
Issue :
1
Database :
Directory of Open Access Journals
Journal :
Journal of Pharmacological Sciences
Publication Type :
Academic Journal
Accession number :
edsdoj.69c03da19ad4bc385443820d53cb4a4
Document Type :
article
Full Text :
https://doi.org/10.1254/jphs.10173FP