Drug-induced potentiation of prepulse inhibition of acoustic startle reflex in mice: a model for detecting antipsychotic activity?

Rationale: Schizophrenic patients typically have impaired startle habituati on (SH) and prepulse inhibition of the startle reflex (PPI). PPI can be dis rupted in rats by psychomimetics, and drug-induced reversal of this deficit is considered to predict potential antipsychotic properties. Certain strai ns of mice, such as C57BL/6J, naturally display poor PPI. Objective: To tes t whether mice spontaneously showing low levels of PPI might prove a useful tool for detecting novel antipsychotics. Methods: PPI and SH were evaluate d in four strains of mice: BALB/cByJ, MORO, 129/SvEv and C57BL/6J. The effe cts of antipsychotic [haloperidol (1, 3 and 6 mg/kg), clozapine (0.3, 1, 3 and 30 mg/kg) and risperidone (0.1, 0.3 and 1 mg/kg,)] and non-antipsychoti c [diazepam (3, 10 and 30 mg/kg), buspirone (1, 3 and 10 mg/kg), desipramin e (3, 10 and 30 mg/kg), morphine (3, 10 and 30 mg/kg) and scopolamine (0.3, 1 and 3 mg/kg)] drug treatments were studied on PPI. Results: Haloperidol (6 mg/kg), clozapine (3 and 30 mg/kg), and risperidone (1 mg/kg) all signif icantly enhanced PPI in C57BL/6J. All non-antipsychotics failed to improve PPI in this strain, except diazepam. Facilitation of PPI was also obtained in the other strains; however, clear interstrain differences were observed depending on the class of antipsychotic used and on the level of prepulse i ntensity. Conclusion: Anti psychotic-induced facilitation of PPI is clearly detected in mice naturally exhibiting poor levels of sensorimotor gating ( e.g., C57BL/6J), but is also observed in other strains of mice. The use of this procedure as a potential screening test for detecting novel antipsycho tic medications is discussed.