Evidence map›Paper›PMID 33242572›Full record

ArticleProgress in neurobiology2021

The environmental sculpting hypothesis of juvenile and adult hippocampal neurogenesis.

Jesse D Cushman, Michael R Drew, Franklin B Krasne

Abstract read
In one paragraph

Article in Progress in neurobiology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

16 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
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  7. T-Type CaThe Journal of neuroscience : the official journal of the Society for Neuroscience · 2024
    Article
  8. Article
  9. Neuron and Brain Maturation 2.0.International journal of molecular sciences · 2023
    Article
  10. Review
  11. Article
  12. Article
  13. Review
  14. Review
  15. Article
  16. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Jesse D CushmanNeurobehavioral Core Laboratory, National Institute of Environmental Health Sciences, National Institutes of Health, Durham, NC 27709, United States. Electronic address: jesse.cushman@nih.gov.
Michael R DrewCenter for Learning and Memory, Department of Neuroscience, University of Texas at Austin, Austin, TX 78712, United States. Electronic address: mdrew@utexas.edu.
Franklin B KrasneDepartment of Psychology, University of California Los Angeles, Box 951563, Los Angeles, CA 90095-1563, United States. Electronic address: krasne@psych.ucla.edu.

Funding

Neurobehavioral Core LaboratoryZICES103330 · NIEHS · NATIONAL INSTITUTE OF ENVIRONMENTAL HEALTH SCIENCES · PI CUSHMAN, JESSE · 2018 to 2025
$13.3M
Contextual Fear Differentiation, Sex Differences and AcetylcholineR01MH062122 · NIMH · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI FANSELOW, MICHAEL S · 2001 to 2021
$7.3M
Hippocampal Mechanisms of Fear ExtinctionR01MH117426 · NIMH · UNIVERSITY OF TEXAS AT AUSTIN · PI DREW, MICHAEL R · 2019 to 2023
$1.9M
Role of adult hippocampal neurogenesis in memoryR01MH102595 · NIMH · UNIVERSITY OF TEXAS AT AUSTIN · PI DREW, MICHAEL R · 2014 to 2018
$1.9M
NIMH NIH HHS R01 MH062122NIMH NIH HHS R01 MH102595NIMH NIH HHS R01 MH117426
6 · The paper itself

Abstract

We propose that a major contribution of juvenile and adult hippocampal neurogenesis is to allow behavioral experience to sculpt dentate gyrus connectivity such that sensory attributes that are relevant to the animal's environment are more strongly represented. This "specialized" dentate is then able to store a larger number of discriminable memory representations. Our hypothesis builds on accumulating evidence that neurogenesis declines to low levels prior to adulthood in many species. Rather than being necessary for ongoing hippocampal function, as several current theories posit, we argue that neurogenesis has primarily a prospective function, in that it allows experience to shape hippocampal circuits and optimize them for future learning in the particular environment in which the animal lives. Using an anatomically-based simulation of the hippocampus (BACON), we demonstrate that environmental sculpting of this kind would reduce overlap among hippocampal memory representations and provide representation cells with more information about an animal's current situation; consequently, it would allow more memories to be stored and accurately recalled without significant interference. We describe several new, testable predictions generated by the sculpting hypothesis and evaluate the hypothesis with respect to existing evidence. We argue that the sculpting hypothesis provides a strong rationale for why juvenile and adult neurogenesis occurs specifically in the dentate gyrus and why it declines significantly prior to adulthood.

Indexed as

HippocampusNeurogenesisAgingAnimalsLearningProspective StudiesAdult neurogenesisDentate gyrusHippocampusMemory

Identifiers

PMID33242572
PMCPMC8562867

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.