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[Afobazole decreases motor side effects induced by haloperidol]
Eksperimental'Naia I Klinicheskaia Farmakologiia
|April 2, 2009
Summary
Anxiolytic afobazole potentiates haloperidol effects in mice but reduces its extrapyramidal side effects in rats and mice with repeated dosing. This suggests afobazole
Area of Science:
- Neuropharmacology
- Behavioral Neuroscience
Context:
- Haloperidol, a typical antipsychotic, induces extrapyramidal symptoms (EPS) and motor disturbances.
- Afobazole is an anxiolytic drug with potential interactions with dopaminergic and sigma 1 receptors.
Purpose:
- To investigate the effects of afobazole on haloperidol-induced motor behaviors in rodents.
- To explore the potential of afobazole in mitigating haloperidol-induced side effects.
Summary:
- A single dose of afobazole (10 mg/kg) enhanced haloperidol's effect in the apomorphine-induced climbing test in mice but did not affect haloperidol-induced catalepsy.
- Repeated daily administration of afobazole (10 mg/kg) for five days reduced haloperidol-induced extrapyramidal effects in both rats and mice, without altering apomorphine-induced climbing.
- Afobazole's ability to reduce haloperidol-induced extrapyramidal disturbances may be linked to its agonist activity at sigma 1 receptors.
Impact:
- Afobazole demonstrates a dose- and duration-dependent modulation of haloperidol's effects.
- Findings suggest afobazole as a potential adjunct therapy to manage antipsychotic-induced motor side effects.
- The study highlights the role of sigma 1 receptors in mediating these neuropharmacological interactions.
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