ABSTRACT
Retinoic acid (RA) is a biologically active form of vitamin A. Teratogenicity has been observed in pregnant mammals exposed to high doses of vitamin A. We investigated the distribution of nitrergic neurons in rat prefrontal cortex (PFC) at developmental stages 7 days to young adulthood under physiological conditions and after prenatal application of all trans-RA. The neurons were studied histochemically using NADPH-diaphorase, which stains neurons dark blue. We found that nitrergic neurons differentiate rapidly and reach structural maturity by the end of the second week of postnatal development. We found that the processes of the neurons of nitrergic neurons of 14-day-old rats in the RA group were shorter than those of the control group. Our findings suggest that excess RA during the prenatal period may influence the development and morphology of NADPH-diaphorase positive neurons, probably by RA-specific receptors in the PFC of 14-day-old rats. RA receptors may be the main effector molecules responsible for the changes of dendrite length induced by all-trans RA. During later development, changes are not observed, probably due to maturation of the nervous system.
