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Science· 2014Q1

Hippocampal Neurogenesis Regulates Forgetting During Adulthood and Infancy

Katherine G. Akers, Alonso Martínez-Canabal, Leonardo Restivo, Adelaide P. Yiu et al.

Short summary

New neurons in the hippocampus actively cause forgetting of existing memories in adult mice, a process that can be reversed by reducing neurogenesis.

AI-generated from the title and abstract; the full text is not read.

Key points

  • Increasing hippocampal neurogenesis in adult mice induced forgetting of existing memories.
  • Decreasing neurogenesis in infant mice mitigated infantile amnesia.
  • Manipulating neurogenesis levels induced infantile amnesia in species that normally do not exhibit it.
  • Neurogenesis actively remodels hippocampal circuits, leading to memory degradation.

AI-generated from the title and abstract; the full text is not read.

Abstract

Throughout life, new neurons are continuously added to the dentate gyrus. As this continuous addition remodels hippocampal circuits, computational models predict that neurogenesis leads to degradation or forgetting of established memories. Consistent with this, increasing neurogenesis after the formation of a memory was sufficient to induce forgetting in adult mice. By contrast, during infancy, when hippocampal neurogenesis levels are high and freshly generated memories tend to be rapidly forgotten (infantile amnesia), decreasing neurogenesis after memory formation mitigated forgetting. In precocial species, including guinea pigs and degus, most granule cells are generated prenatally. Consistent with reduced levels of postnatal hippocampal neurogenesis, infant guinea pigs and degus did not exhibit forgetting. However, increasing neurogenesis after memory formation induced infantile amnesia in these species.

The authors' abstract, as published at the source. Science, 2014 · DOI ↗

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Field: Developmental Neuroscience

Developmental NeuroscienceNeuroscience