Recent evidence has shown that perinatal administration of zidovudine (AZT)
to HIV-infected mothers reduces the risk of maternal-infant transmission o
f the virus. Treatment of pregnant seropositive women with AZT is becoming
a common medical practice, despite the paucity of information about the pot
ential neurotoxic/behavioral-teratogenic effects of AZT on the developing o
rganism. The aim of the present study is to evaluate in mice the short-, me
dium-, and long-term effects of prenatal exposure to AZT on neurobehavioral
development. Pregnant mice were given 0.2, 0.4, and 2.0 mg/ml AZT in drink
ing water from day 10 of gestation to delivery. Offspring's viability was s
everely affected in the 2.0 mg/ml AZT group. Thus, behavioral analysis was
carried out in offspring of 0.2 and 0.4 mg/ml AZT treated females only. Som
e limited but significant alterations were found, such as stunted body weig
ht, delayed appearance of the pole-grasping reflex, and a slight impairment
in the acquisition phase of a passive avoidance response. Moreover, sexual
differences in some items of the social behavior repertoire appeared to be
affected by AZT treatment. (C) 1999 Elsevier Science Inc. All rights reser
ved.