Evidence map›Paper›PMID 20954935›Full record

ArticleJournal of cognitive neuroscience2011

Learning increases the survival of newborn neurons provided that learning is difficult to achieve and successful.

Daniel M Curlik, Tracey J Shors

Open access · bronzeAbstract read
In one paragraph

Article in Journal of cognitive neuroscience, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
2.2field-weighted citation impact, top 13% of its field
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

28 citing papers in PubMed, 63 citations in OpenAlex.

  1. Trial
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  5. Article
  6. Review
  7. Behavioral and structural adaptations to stress.Frontiers in neuroendocrinology · 2018
    Review
  8. Cortical spreading depolarization increases adult neurogenesis, and alters behavior and hippocampus-dependent memory in mice.Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism · 2017
    Article
  9. Review
  10. Article
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  15. Physical performance and disability in schizophrenia.Schizophrenia research. Cognition · 2014
    Article
  16. Article
  17. Article
  18. Article
  19. Neuronal Rac1 is required for learning-evoked neurogenesis.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2013
    Article
  20. 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

2 authors at 1 institution in 1 country.

Daniel M CurlikDepartment of Psychology and Center for Collaborative Neuroscience, Rutgers University, 152 Frelinghuysen Road, Piscataway, NJ 08854-8020, USA.
Tracey J Shors
Rutgers, The State University of New Jersey · US

Funding

Stress and Memory Formation Across the Female LifespanR01MH059970 · NIMH · RUTGERS THE ST UNIV OF NJ NEW BRUNSWICK · PI SHORS, TRACEY J · 1998 to 2009
$2.5M
NIMH NIH HHS 3R01MH059970-10S1NIMH NIH HHS MH-59970NIMH NIH HHS R01 MH059970
6 · The paper itself

Abstract

Learning increases neurogenesis by increasing the survival of new cells generated in the adult hippocampal formation [Shors, T. J. Saving new brain cells. Scientific American, 300, 46-52, 2009]. However, only some types of learning are effective. Recent studies demonstrate that animals that learn the conditioned response (CR) but require more trials to do so retain more new neurons than animals that quickly acquire the CR or that fail to acquire the CR. In these studies, task parameters were altered to modify the number of trials required to learn a CR. Here, we asked whether pharmacological manipulations that prevent or facilitate learning would decrease or increase, respectively, the number of cells that remain in the hippocampus after training. To answer this question, we first prevented learning with the competitive N-methyl-D-aspartate (NMDA) receptor antagonist (RS)-3-(2-carboxypiperazin-4-yl) propyl-1-phosphonic acid. As a consequence, training did not increase cell survival. Second, we facilitated learning with the cognitive enhancer D-cycloserine, which increases NMDA receptor activity via its actions at the glycine binding site. Administration of D-cycloserine each day before training increased the number of learned responses and the number of cells that survived. All animals that learned the CR retained more of the new cells, but those that learned very quickly retained fewer than those that required more training trials to learn. Together, these results demonstrate that NMDA receptor activation modifies learning and as a consequence alters the number of surviving cells in the adult hippocampus.

Indexed as

Analysis of VarianceAnimalsBromodeoxyuridineCell CountCell SurvivalConditioning, EyelidExcitatory Amino Acid AntagonistsHippocampusMaleMaze LearningNeurogenesisNeuronsPiperazinesRatsRats, Sprague-DawleyReceptors, N-Methyl-D-Aspartate3-(2-carboxypiperazin-4-yl)propyl-1-phosphonic acidBromodeoxyuridineExcitatory Amino Acid AntagonistsPiperazinesReceptors, N-Methyl-D-Aspartate

Identifiers

PMID20954935
PMCPMC3289535
OpenAlexW2163067175

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

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.