Forgetting at biologically realistic levels of neurogenesis in alarge-scale hippocampal model.

Neurogenesis persists throughout life in the dentate gyrus region of the mammalian hippocampus. Computational models have established that the addition of neurons degrades existing memories (i.e., produces forgetting). These predictions are supported by empirical observations in rodents, where post-training increases in neurogenesis also promote forgetting of hippocampus-dependent memories. However, in these computational models which use 10-1,000 neurons to represent the dentate gyrus, forgetting is only observed at rates of new neuron addition that greatly exceed adult neurogenesis rates observed in vivo. In order to address this, here we generated an artificial neural network which incorporated more realistic features of the hippocampus – including increased network size (with up to 20,000 dentate gyrus neurons), sparse activity, and sparse connectivity – features that were not present in earlier models. In addition, we explored how properties of new neurons – their connectivity, excitability, and plasticity – impact forgetting using a pattern categorization task. Our results revealed that neurogenic networks forget previously learned input-output pattern associations. This forgetting predicted a performance enhancement in subsequent conflictual learning, compared to static networks (with no added neurons). These effects were especially sensitive to changes in increased output connectivity and excitability of new neurons. Crucially, forgetting was observed at much lower rates of neurogenesis in larger networks, with the addition of as little as 0.2% of the total DG population sufficient to induce forgetting.