A variety of drug classes, including psychomotor stimulants and antide
pressants, interact with monoamine transporters in order to exert thei
r effects. Although these transporters have been extensively character
ized in the adult brain, little is known about uptake mechanisms in th
e fetal system. High affinity dopamine (DA) and serotonin (5-HT) uptak
e in the striatum and frontal cortex, respectively, were examined in r
at fetuses (embryonic day 20; E-2O). These results were then compared
to uptake in adult rat synaptosomal preparations of the same regions.
The data indicate that the fetal (E-20) uptake mechanism is sodium-dep
endent. Furthermore, the potency of various agents to inhibit transpor
ter function was assessed. These drugs produced a concentration-depend
ent inhibition of uptake, and the resulting IC50 values were not signi
ficantly different from those obtained in the adult preparations. Our
results provide evidence that the affinity of monoamine uptake inhibit
ors for fetal (E-20) DA and 5-HT transporters is similar to that obser
ved with adult transporters. This observation has broad implications w
hen considering neuronal development and in utero exposure to drugs th
at exert their effects through these transporters.