Wk. Cullen et Mj. Rowan, GEPIRONE AND 1-(2-PYRIMIDINYL)-PIPERAZINE-INDUCED REDUCTION OF AVERSIVELY EVOKED ULTRASONIC VOCALIZATION IN THE RAT, Pharmacology, biochemistry and behavior, 48(1), 1994, pp. 301-306
Ultrasonic (22 kHz) vocalisation in response to a mildly aversive foot
shock was measured in the dark compartment of a light-dark box both i
mmediately and 24 h after the shock. Gepirone (1 and 5 mg/kg, IP) prod
uced a reduction in the duration of vocalisation at both times. Althou
gh a metabolic inhibitor, proadifen (40 mg/kg) did not reduce this eff
ect of gepirone, the gepirone hepatic metabolite, 1-(2-pyrimidinyl)-pi
perazine (1-PP, 1 mg/kg), was also active in the test. Performance of
a 24 h step-through passive avoidance task was impaired by gepirone on
ly at a dose, 5 mg/kg, which also reduced spontaneous locomotor and re
aring activity in the apparatus. It would appear that mild foot shock-
evoked ultrasonic vocalisation may provide a more sensitive indicator
of the effect of gepirone and related drugs on the affective response
of rats to aversive stimulation.