EFFECTS OF CHLORDIAZEPOXIDE, BUSPIRONE AND THE 5-HT(3) RECEPTOR ANTAGONIST, BRL-46470, ON THE BEHAVIOR OF ESTROUS AND DIESTRUS FEMALE MICE WHEN ENCOUNTERING MALE PARTNERS
B. Gao et Mg. Cutler, EFFECTS OF CHLORDIAZEPOXIDE, BUSPIRONE AND THE 5-HT(3) RECEPTOR ANTAGONIST, BRL-46470, ON THE BEHAVIOR OF ESTROUS AND DIESTRUS FEMALE MICE WHEN ENCOUNTERING MALE PARTNERS, Neuropharmacology, 32(10), 1993, pp. 969-975
Ethological procedures were employed to examine the differences in beh
aviour between oestrous and dioestrous control mice, and to investigat
e the changes to behavioural responsiveness in oestrous and dioestrous
mice induced by treatment with the anxiolytic compounds, chlordiazepo
xide (CDP, 21.5mg/1), buspirone (12.8mg/1) and the 5-HT3 receptor anta
gonist, BRL 46470 (40,ug/1). Compounds were given in drinking fluid fo
r 6-8 days prior to behavioural observations (average daily intake: CD
P-5 mg/kg; buspirone-2.5 mg/kg; BRL 46470-10 mug/kg). Behaviour of the
females was examined in the ''approach-avoidance'' situation of 5 min
encounters with an unfamiliar male in a neutral cage. Oestrous contro
ls spent more time in social investigation, sniffing of the substrate
and scanning than dioestrous controls and spent less time in digging a
nd exploration. Each of the anxiolytic compounds, CDP, buspirone and B
RL 46470, significantly raised the duration of social investigation bo
th in oestrous and dioestrous females. Each of these compounds also in
creased the duration of ''digging'' by oestrous females, and duration
of the social element ''investigate'' in dioestrous females. Effects o
n the occurrence of other individual elements within each behavioural
category depended on the anxiolytic compound administered and the stag
e of the ovarian cycle at the time of testing. There were few signific
ant differences between the behaviour of the male partners in each gro
up. It is concluded that in this paradigm both oestrous and dioestrous
females are sensitive to the enhancement of social investigation by a
nxiolytic compounds and that the use of female mice in this test situa
tion may provide a potentially useful method in drug screening.