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During adulthood, new neurons are continuously added to the mammalian dentate gyrus (DG). An increasing number of studies have correlated changes in rates of dentate neurogenesis with memory abilities. One study based on subchronic treatment with the toxin methylazoxymethanol acetate (MAM) has provided causal evidence that neurogenesis is involved in hippocampal-dependent trace conditioning. In contrast, spatial learning is not impaired following MAM treatment. We hypothesized that this was due to the small residual number of new cells produced following MAM treatment. In the present experiment, we attempted to achieve a higher level of reduction of adult-generated cells following MAM treatment in young and aged rats. We found only a partial reduction of adult-generated cells in the DG. More importantly, independently of the age of the animals, MAM treatment at a dose necessary to reduce neurogenesis altered the overall health of the animals. In conclusion, the behavioural results obtained following subchronic treatment with high doses of MAM in adulthood must be interpreted with extreme caution.

Original publication




Journal article


Eur J Neurosci

Publication Date





778 - 783


Age Factors, Aging, Analysis of Variance, Animals, Behavior, Animal, Body Weight, Bromodeoxyuridine, Cell Count, Cell Proliferation, Dentate Gyrus, Dose-Response Relationship, Drug, Immunohistochemistry, Ki-67 Antigen, Male, Methylazoxymethanol Acetate, Microtubule-Associated Proteins, Motor Activity, Neurons, Neuropeptides, Protein Synthesis Inhibitors, Psychomotor Performance, Rats, Rats, Sprague-Dawley, Reaction Time, Time Factors