The rabbit has been used to model the potential effects of in utero ex
posure to cocaine on fetal and postnatal development, Special advantag
es of this animal model include the fact that cocaine can be easily ad
ministered intravenously, thus mimicking crack cocaine use by pregnant
women. Results indicate that at the dosage used (8 mg\kg of body weig
ht, given intravenously daily) gross teratologic defects do not develo
p. Cocaine-exposed pregnant does do not differ from controls in weight
gain or in the number of live kits delivered. Cocaine-exposed kits do
not differ from controls in survival or in postnatal weight gain. The
importance of this rabbit model is that offspring that have been expo
sed to these doses of cocaine in utero have a variety of abnormalities
in structure and function of the central nervous system in the absenc
e of any major teratologic defects.