THE EFFECTS OF BUSPIRONE ON THE BEHAVIOR OF CONTROL AND STRESSED MICE

Citation
P. Pokk et A. Zharkovsky, THE EFFECTS OF BUSPIRONE ON THE BEHAVIOR OF CONTROL AND STRESSED MICE, Journal of Physiology and Pharmacology, 49(1), 1998, pp. 175-185
Citations number
50
Categorie Soggetti
Physiology
ISSN journal
08675910
Volume
49
Issue
1
Year of publication
1998
Pages
175 - 185
Database
ISI
SICI code
0867-5910(1998)49:1<175:TEOBOT>2.0.ZU;2-8
Abstract
The effects of buspirone on the locomotor activity and behaviour in th e plus-maze and hole-board tests were studied in control and small pla tform stressed mice. Small platform stress for 24 hours increased the locomotor activity of mice and induced anxiolytic-like effect in the p lus-maze and hole-board tests. Administration of buspirone either did not affect (2.0 and 4.0 mg/kg) or inhibited (8.0 mg/kg) locomotions in control animals. The inhibition of locomotor activity by buspirone wa s greater in small platform stressed mice. In control mice buspirone i n doses 2.0 and 4.0 mg/kg exerted anxiolytic effect in the plus-maze a nd hole board test that was reflected by an increase in the percentage of entries onto and the percentage of time spent on the open arms of the plus-maze and increased number of head-dippings in the hole-board test. In contrast, in small platform stressed mice, buspirone did not induce anxiolytic action in the plus-maze and hole-board tests at any dose tested. In doses 2.0 and 4.0 mg/kg buspirone produced a sedative effect that was reflected by a decrease in the total number of entries made onto the open and into the closed arms of the plus-maze and a de crease in the number of head-dippings and rearins in the hole-board te st. These data suggest that small platform stress induces a sensitizat ion of mice to the motor depressant effect of buspirone. At the same t ime small platform stress induces hyposensitivity to the anxiolytic ef fect of buspirone. It is proposed that these changes might be due to a lterations in the serotonergic transmission or to changes in the relea se of corticosterone.