There is increasing evidence that genetic factors can influence indivi
dual differences in vulnerability to drugs of abuse(1,2). Serotonin (5
-hydroxytryptamine, 5-HT), acting through many receptors can modulate
the activity of neural reward pathways and thus the effects of various
drugs of abuse(3-8). Here we examine the effects of cocaine in mice l
acking one of the serotonin-receptor subtypes, the 5-HT1B receptor(9).
We show that mice lacking 5-HT1B display increased locomotor response
s to cocaine and that they are more motivated to self-administer cocai
ne. We propose that even drug-naive 5-HT1B-knockout mice are in a beha
vioural and biochemical state that resembles that of wild-type mice se
nsitized to cocaine by repeated exposure to the drug. This altered sta
te might be responsible for their increased vulnerability to cocaine.