The anxiolytic potential of the putative neuroleptic sertindole was as
sessed in various animal models of anxiety in rodents and in the marmo
set human threat test. Sertindole facilitates the exploratory behaviou
r of mice and rats in the black and white two-compartment box over a l
arge dose range. Sertindole is more potent than diazepam, i.e., minima
l effective doses (MED) in the mouse are 0.00023 nmol (0.1 ng/kg) and
0.46 mu mol/kg (0.13 mg/kg), respectively, and MED in the rat are 0.23
nmol/kg (0.10 mu g/kg) and 35 nmol/kg (10 mu g/kg), respectively. Ser
tindole increases the time that pairs of rats spend in active social i
nteraction (unfamiliar high light conditions) at extremely low doses (
MED = 0.000023 nmol/kg [0.01 ng/kg]) being some 19 million-fold more a
ctive than diazepam (MED = 0.44 mu mol/kg; 0.13 mg/kg). Sertindole inh
ibits isolation-induced aggressive behaviour in the mouse, but only at
high doses, and sertindole does not inhibit shock-induced suppression
of drinking or footshock-induced ultrasonic vocalization in the rat.
Sertindole similarly shows potent anxiolytic-like activity in the marm
oset human threat test (MED = 23 nmol/kg; 10 mu g/kg). The range betwe
en anxiolytic doses and sedative doses is very large for sertindole, i
.e., sedation is observed at 2,300 nmol/kg (1 mg/kg). (C) 1995 Wiley-L
iss, Inc.