Evidence map›Paper›PMID 39271752›Full record

ArticleMolecular psychiatry2025

Spatio-temporal mechanisms of consolidation, recall and reconsolidation in reward-related memory trace.

Adam Hamed, Miron Bartosz Kursa, Wiktoria Mrozek, Krzysztof Piotr Piwoński, Monika Falińska, Konrad Danielewski, Emilia Rejmak, Urszula Włodkowska, Stepan Kubik, Rafał Czajkowski

Abstract read
In one paragraph

Article in Molecular psychiatry, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. 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

10 authors.

Adam Hamed *Laboratory of Spatial Memory, Nencki Institute of Experimental Biology, Polish Academy of Sciences, Warsaw, Poland. a.hamed@nencki.edu.pl.ORCID 0000-0003-1477-9177
Miron Bartosz Kursa *Interdisciplinary Centre for Mathematical and Computational Modelling, University of Warsaw, Warsaw, Poland.ORCID 0000-0001-7672-648X
Wiktoria MrozekLaboratory of Spatial Memory, Nencki Institute of Experimental Biology, Polish Academy of Sciences, Warsaw, Poland.
Krzysztof Piotr PiwońskiInterdisciplinary Centre for Mathematical and Computational Modelling, University of Warsaw, Warsaw, Poland.
Monika FalińskaLaboratory of Spatial Memory, Nencki Institute of Experimental Biology, Polish Academy of Sciences, Warsaw, Poland.
Konrad DanielewskiLaboratory of Emotions Neurobiology, Nencki Institute of Experimental Biology, Polish Academy of Sciences, Warsaw, Poland.
Emilia RejmakBRAINCITY, Nencki Institute of Experimental Biology, Polish Academy of Sciences, Warsaw, Poland.
Urszula WłodkowskaLaboratory of Spatial Memory, Nencki Institute of Experimental Biology, Polish Academy of Sciences, Warsaw, Poland.ORCID 0000-0003-4132-328X
Stepan KubikInstitute of Physiology, Academy of Sciences of the Czech Republic, Praha, Czechia.
Rafał CzajkowskiLaboratory of Spatial Memory, Nencki Institute of Experimental Biology, Polish Academy of Sciences, Warsaw, Poland. r.czajkowski@nencki.edu.pl.

Funding

Narodowe Centrum Nauki (National Science Centre) Opus 2018/29/B/NZ7/02021Narodowe Centrum Nauki (National Science Centre) Opus Opus 2023/51/B/NZ7/02350Narodowe Centrum Nauki (National Science Centre) Sonata-bis 2014/14/E/NZ4/00172
6 · The paper itself

Abstract

The formation of memories is a complex, multi-scale phenomenon, especially when it involves integration of information from various brain systems. We have investigated the differences between a novel and consolidated association of spatial cues and amphetamine administration, using an in situ hybridisation method to track the short-term dynamics during the recall testing. We have found that remote recall group involves smaller, but more consolidated groups of neurons, which is consistent with their specialisation. By employing machine learning analysis, we have shown this pattern is especially pronounced in the VTA; furthermore, we also uncovered significant activity patterns in retrosplenial and prefrontal cortices, as well as in the DG and CA3 subfields of the hippocampus. The behavioural propensity towards the associated localisation appears to be driven by the nucleus accumbens, however, further modulated by a trio of the amygdala, VTA and hippocampus, as the trained association is confronted with test experience. Moreover, chemogenetic analysis revealed central amygdala as critical for linking appetitive emotional states with spatial contexts. These results show that memory mechanisms must be modelled considering individual differences in motivation, as well as covering dynamics of the process.

Indexed as

Memory ConsolidationMental RecallAmphetamineAmygdalaAnimalsBrainCuesHippocampusMachine LearningMaleMemoryNeuronsNucleus AccumbensPrefrontal CortexRatsRewardAmphetamine

Identifiers

PMID39271752
PMCPMC11919705

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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.