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Dulawa SC, Geyer MA. 
“Psychopharmacology of prepulse inhibition in mice”. 
Chin J Physiol. 1996;39(3):139-46.
The attenuation of the startle response termed 'prepulse inhibition' (PPI) occurs when an abrupt startling stimulus is preceded 30-500 msec by a barely detectable prestimulus or 'prepulse'. PPI provides a measure of sensorimotor gating, which is a short time-constant central processing mechanism that is disrupted in patients with schizophrenia, and a number of other neuropsychiatric disorders. The present experiments examined normal PPI in the mouse, and assessed the effects of apomorphine, d-amphetamine, PCP, and MDMA on mouse PPI. As predicted, mice demonstrated robust and reliable PPI, and each compound tested disrupted PPI. As with rats, 2.0 mg/kg apomorphine, 10.0 mg/kg PCP, and 10.0 mg/kg MDMA disrupted PPI significantly, while 5.0 mg/kg d-amphetamine produced a large reduction of PPI that approached significance. Our findings suggest that the mouse may provide another model system for the study of sensorimotor gating mechanisms.
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