Animal studies as well as clinical studies have suggested that the bra
in 5-HT system is important for the regulation of voluntary ethanol in
take and preference. Previous studies have suggested that 5-HT1A recep
tor agonists may reduce ethanol preference in rats. In the present stu
dy on mice, the 5-HT1A receptor agonists (8-OH-DPAT), ipsapirone, and
buspirone all antagonized the locomotor activity (LMA) stimulatory eff
ect of ethanol (2.5 g/kg). The present results provide further support
for the notion that the LMA-increasing effect of ethanol may be homol
ogous to its reinforcing properties and that 5-HT1A receptor agonists
may counteract these properties as well.