MK801, an NMDA antagonist, blocks acquisition of a spatial task but does not block maternal experience effects.

Two studies were conducted to determine the effect on learning and memory of MK801, an N-methyl-D-aspartate (NMDA) antagonist that acts through noncompetitive blockade of the ion channel associated with the NMDA receptor. In the first study we found a dose-dependent impairment in the acquisition of a modified radial-arm maze task, resulting from injections (IP) of MK801 10 minutes prior to training. The retention of that learning, as measured by the amount of training required for reacquisition on the following day, was unaffected by the drug. In contrast, in the second study, MK801 did not block the experience-based facilitation of maternal responding seen 8 days after one hour of exposure to pups: experienced dams showed facilitated onset of maternal behavior, relative to inexperienced dams, regardless of the drug they received. However, injections of MK-801, either just before or just after the maternal experience, did lead to some deficits in maternal responding on the first day of testing. We have previously shown that these maternal experience effects are blocked by injections (ICV, SC) of cycloheximide, a protein synthesis inhibitor. These results suggest that the NMDA system does not mediate all, if any, of cycloheximide's effects on maternal experience and, furthermore, that the NMDA system may mediate some but not all forms of learning.

Effects of cycloheximide on the retention of olfactory learning and maternal experience effects in postpartum rats.

We have previously shown that cycloheximide, a protein synthesis inhibitor, blocks retention of experimentally based material responding in postpartum rats. In the following study, we investigated further the effect of this drug on maternal experience effects and, in particular, on the retention of olfactory learning. Dams were injected SC with cycloheximide or saline following a one-hour maternal experience with pups scented with one of two artificial odorants. When tested eight days later, saline but not cycloheximide animals demonstrated a preference for the odor which they had experience on pups. Animals were then tested for maternal responsiveness with pups that were scented with an odor that was either the same or different from the one used in the maternal experience. All animals receiving cycloheximide, regardless of the pup odor at testing, exhibited long latencies to become maternal, replicating our earlier finding that the retention of learning in maternal behavior is susceptible to disruption by protein synthesis inhibitors. A similar disruption of the experience effect was found when the pup odor at testing was different from the exposure odor. This suggests that olfactory learning may normally play a role in the mediation of postpartum experience effects.

Fetal uterine position affects copulation and scent marking by adult male gerbils.

Those male Mongolian gerbils (Meriones unguiculatus) that as fetuses resided in uterine locations adjacent to no females, when adult, scent marked more frequently, mounted estrous females with shorter latencies, and ejaculated after fewer intromissions than did those male gerbils that as fetuses resided in uterine locations adjacent to two females. Both the scent-marking frequencies and copulatory patterns of adult males were positively correlated with three indices of their circulating levels of testosterone: ventral gland size, anogenital distance, and relative testes weights. Also, those males that scent marked relatively frequently copulated more reliably than did those males that scent marked relatively infrequently.