Evidence map›Paper›PMID 22016545›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2011

Posttraining ablation of adult-generated neurons degrades previously acquired memories.

Maithe Arruda-Carvalho, Masanori Sakaguchi, Katherine G Akers, Sheena A Josselyn, Paul W Frankland

Abstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 105 papers.

0numbers the graph read from it
0cells of the map it votes in
105citing 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

105 citing papers in PubMed.

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  7. Cognitive Flexibility Is Selectively Impaired by Radiation and Is Associated with Differential Recruitment of Adult-Born Neurons.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2023
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45 more citing papers are in PubMed but not listed here.

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

5 authors.

Maithe Arruda-CarvalhoProgram in Neurosciences and Mental Health, The Hospital for Sick Children, Toronto, Canada.
Masanori Sakaguchi
Katherine G Akers
Sheena A Josselyn
Paul W Frankland

Funding

Canadian Institutes of Health Research MOP74650Canadian Institutes of Health Research MOP86762
6 · The paper itself

Abstract

New neurons are continuously generated in the subgranular zone of the adult hippocampus and, once sufficiently mature, are thought to integrate into hippocampal memory circuits. However, whether they play an essential role in subsequent memory expression is not known. Previous studies have shown that suppression of adult neurogenesis often (but not always) impairs subsequent hippocampus-dependent learning (i.e., produces anterograde effects). A major challenge for these studies is that these new neurons represent only a small subpopulation of all dentate granule cells, and so there is large potential for either partial or complete compensation by granule cells generated earlier on during development. A potentially more powerful approach to investigate this question would be to ablate adult-generated neurons after they have already become part of a memory trace (i.e., retrograde effects). Here we developed a diphtheria toxin-based strategy in mice that allowed us to selectively ablate a population of predominantly mature, adult-generated neurons either before or after learning, without affecting ongoing neurogenesis. Removal of these neurons before learning did not prevent the formation of new contextual fear or water maze memories. In contrast, removal of an equivalent population after learning degraded existing contextual fear and water maze memories, without affecting nonhippocampal memory. Ablation of these adult-generated neurons even 1 month after learning produced equivalent memory degradation in the water maze. These retrograde effects suggest that adult-generated neurons form a critical and enduring component of hippocampal memory traces.

Indexed as

AnimalsAntineoplastic Agents, HormonalAvoidance LearningBehavior, AnimalBromodeoxyuridineCalcium-Binding ProteinsCell Line, TransformedCell ProliferationCell SurvivalConditioning, PsychologicalDentate GyrusDiphtheria ToxinDiscrimination, PsychologicalDoublecortin Domain ProteinsEstrogen Receptor alphaFear1-phenyl-1,4-epoxy-1H,4H-naphtho(1,8-de)(1,2)dioxepinAif1 protein, mouseAntineoplastic Agents, HormonalBromodeoxyuridineCalcium-Binding ProteinsDiphtheria ToxinDoublecortin Domain ProteinsEstrogen Receptor alphaHbegf protein, mouseHeparin-binding EGF-like Growth FactorIntercellular Signaling Peptides and ProteinsIntermediate Filament ProteinsMembrane Transport ProteinsMicrofilament ProteinsMicrotubule-Associated ProteinsNaphthalenesNerve Tissue ProteinsNes protein, mouseNestinNeuropeptidesOxepinsTamoxifen

Identifiers

PMID22016545
PMCPMC6623574

What OpenQuestion holds

Textmetadata
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.