Event Abstract Back to Event Associative learning enhances the survival of new neurons in the male and female hippocampus Christina Dalla1, 2* and Tracey J. Shors2 1 Medical School, University of Athens, Department of Pharmacology, Greece 2 Rutgers University, Department of Psychology and Centre for Neurosciences, United States Two decades ago, it was discovered that certain areas of the adult brain give birth to new neurons, a phenomenon called adult neurogenesis. Research in animals has shown that many of these new cells die within a few weeks, unless the animals learn certain types of complex tasks or are living in an enriched environment. Studies from our lab have shown that new cells in the hippocampus, a brain region involved in learning and memory, are more likely to survive if the animals learn a type of task that is difficult to learn. Specifically, learning during an associative task, which depends on the hippocampus (i.e. trace eyeblink conditioning), increases the survival of new cells that were generated in the hippocampus one week before the training experience [1, 2]. On the other hand, training with delay conditioning, which does not depend on the hippocampus and it is easier to learn, does not enhance the survival of the new cells. This phenomenon was first described for male rats, but it was recently confirmed in females [3]. Interestingly, females learn better than males when they are trained to associate stimuli across time, such as during the trace eyeblink conditioning task. As a consequence, more new neurons per unit volume remain in their hippocampus than in males. Furthermore, in individual animals of both sexes, the number of surviving cells correlates positively with asymptotic performance; those that express more learned responses retain more new neurons. However, animals that learn very well retain even more new cells if they require many trials to do so. Once rescued from death, most of the new cells differentiate into neurons, which become functionally integrated into the existing circuitry of the hippocampus. These new cells might be important for new learning experience or for memory. Furthermore, data on males and females suggest that sex differences in learning can contribute to structural sex differences in the adult brain. This work was supported by National Institutes of Health and National Science Foundation grants to T. J. Shors and a Marie Curie International Fellowship to C. Dalla, within the 6th European Community Framework Programme.
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