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Stress and hippocampal neurogenesis
Biological Psychiatry
|December 22, 1999
Summary
The dentate gyrus, crucial for memory, is sensitive to stress. Chronic stress inhibits new neuron growth in this brain region, potentially altering hippocampal function long-term.
Area of Science:
- Neuroscience
- Developmental Biology
- Cell Biology
Background:
- The dentate gyrus (DG) exhibits prolonged development from gestation through adulthood.
- Adult neurogenesis in the DG is conserved across mammalian species.
- This extended development renders the DG susceptible to environmental influences.
Purpose of the Study:
- To review the unique developmental trajectory of the dentate gyrus.
- To explore the impact of environmental factors, particularly stress, on DG development and function.
- To discuss the long-term consequences of early life events on hippocampal function.
Main Methods:
- Review of existing literature on dentate gyrus development and adult neurogenesis.
- Analysis of studies investigating the role of adrenal steroids and stress on granule cell precursor proliferation.
- Examination of the mechanisms underlying stress-induced inhibition of neurogenesis.
Main Results:
- Granule cell production in the DG is modulated by circulating adrenal steroids.
- Glucocorticoids inhibit proliferation via an NMDA receptor-dependent pathway.
- Stressful experiences elevate glucocorticoids, inhibit precursor proliferation, and alter DG structure.
Conclusions:
- The dentate gyrus's protracted development makes it vulnerable to environmental perturbations.
- Chronic stress leads to sustained inhibition of neurogenesis and structural changes in the DG.
- Stress-induced alterations in DG neurogenesis may be a mechanism by which stress impacts hippocampal function.