Journal
BASIC & CLINICAL PHARMACOLOGY & TOXICOLOGY
Volume 112, Issue 3, Pages 192-197Publisher
WILEY-BLACKWELL
DOI: 10.1111/bcpt.12017
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Funding
- Special Program on University Medicine of the Swiss National Science Foundation [33CM30]
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Facilitation of spinal GABAergic inhibition with benzodiazepines (BZDs) reverses pain sensitization in animals; however, the use of BZDs in man is limited by their sedative effect. The antihyperalgesic effects of GABAA agonists are mediated by GABAA receptors containing 2 subunits, whereas sedation is linked to 1 subunit-containing receptors. 2 and 3 selective GABAA receptor modulators have been tested in animals but are not yet available for use in human beings. Clobazam is a 1,5-BZD, which exhibits less cognitive side effects than other benzodiazepines. Here, we studied its antihyperalgesic effects in a mouse model of neuropathic pain. Clobazam showed a dose-dependent antihyperalgesic effect in the chronic constriction injury (CCI) model of neuropathic pain, peaking at 1hr after administration and lasting for 4hr with no relevant sedation at a dose of 3mg/kg. At higher doses, the antihyperalgesic effect was stronger, but sedation became significant. The blood and brain kinetics of clobazam were linear over the range of doses tested with a short half-life of the parent compound and a ready penetration of the bloodbrain barrier. Clobazam blood concentrations decreased rapidly, falling below the limit of detection at 120min. after drug application. Its main metabolite, N-desmethyl-clobazam, showed more delayed and prolonged pharmacokinetics, partly explaining why antihyperalgesia persisted when clobazam was no longer detectable in the blood. Considering its therapeutic margin and its pharmacokinetic properties, clobazam would be a valuable compound to assess the role of the GABAergic pathway in pain transmission in human beings.
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