This study examined the effect of cocaine on cell proliferation in the feta
l monkey cerebral wall. Pregnant monkeys received cocaine daily (10 mg/kg,
orally, in fruit treats, at 07.00 h and 19.00 h) beginning on the 40th day
of pregnancy (E40). The control animals received fruit treats only. One set
of monkeys was used to examine the state of cell proliferation in the feta
l cerebral wall at peak cocaine levels. These animals were injected with [H
-3]thymidine intravenously on E73, 1.5 h after the morning drug or placebo
administration. Another set of monkeys was used to determine the state of c
ell proliferation after cocaine concentration declined to ineffective level
s. These animals were injected with [3H]thymidine on the same day of pregna
ncy 10 h after the treatment, Cesarean sections were performed 40 min after
the radioisotope injection, The right hemispheres were processed for autor
adiography. The left hemispheres were used for biochemical analysis of the
radioisotope incorporation into DNA. The third set of monkeys was used to d
etermine whether chronic cocaine treatment extends the timing of neocortica
l neuronogenesis, These monkeys received their final cocaine treatment on E
102 (the last day of normal neocortical neuronogenesis) and were injected w
ith [3H]thymidine 24 h later. On E113, the fetal brains were processed for
emulsion autoradiography. We found a significant decrease in the density of
[H-3]thymidine-labeled cells and in the levels of this radioisotope incorp
oration into DNA in the fetal cerebral wall 1.5 h after cocaine administrat
ion. In contrast, 10 h after cocaine administration we detected a significa
ntly elevated density of radiolabeled cells, and abnormally high levels of
[3H]thymidine incorporation into DNA, This suggests that chronic intermitte
nt administration of cocaine results in significant periodic fluctuations i
n cell production within the fetal cortical proliferative zones, We detecte
d no cocaine-induced extension in neocortical neuronogenesis.