Evidence map›Paper›PMID 32647258›Full record

ArticleScientific reports2020

Flexible use of allocentric and egocentric spatial memories activates differential neural networks in mice.

Arianna Rinaldi, Elvira De Leonibus, Alessandra Cifra, Giulia Torromino, Elisa Minicocci, Elisa De Sanctis, Rosa María López-Pedrajas, Alberto Oliverio, Andrea Mele

Abstract read
In one paragraph

Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed.

  1. Article
  2. Coordinated Representational Drift Across the Mouse Cortex.bioRxiv : the preprint server for biology · 2026
    Article
  3. Article
  4. Article
  5. Allocentric flocking.Nature communications · 2025
    Article
  6. Navigating space and the developing mind.Frontiers in psychology · 2025
    Review
  7. Article
  8. Article
  9. Review
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
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

9 authors.

Arianna Rinaldi *Department of Biology and Biotechnology C. Darwin, Sapienza University of Rome, Rome, Italy. arianna.rinaldi@uniroma1.it.
Elvira De Leonibus *Institute of Cellular Biology and Biochemistry, IBBC-CNR, Naples, Italy.
Alessandra CifraDepartment of Biology and Biotechnology C. Darwin, Sapienza University of Rome, Rome, Italy.
Giulia TorrominoDepartment of Biology and Biotechnology C. Darwin, Sapienza University of Rome, Rome, Italy.
Elisa MinicocciDepartment of Biology and Biotechnology C. Darwin, Sapienza University of Rome, Rome, Italy.
Elisa De SanctisDepartment of Biology and Biotechnology C. Darwin, Sapienza University of Rome, Rome, Italy.
Rosa María López-PedrajasDepartment of Biology and Biotechnology C. Darwin, Sapienza University of Rome, Rome, Italy.
Alberto OliverioDepartment of Biology and Biotechnology C. Darwin, Sapienza University of Rome, Rome, Italy.
Andrea MeleDepartment of Biology and Biotechnology C. Darwin, Sapienza University of Rome, Rome, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Goal-directed navigation can be based on world-centered (allocentric) or body-centered (egocentric) representations of the environment, mediated by a wide network of interconnected brain regions, including hippocampus, striatum and prefrontal cortex. The relative contribution of these regions to navigation from novel or familiar routes, that demand a different degree of flexibility in the use of the stored spatial representations, has not been completely explored. To address this issue, we trained mice to find a reward relying on allocentric or egocentric information, in a modified version of the cross-maze task. Then we used Zif268 expression to map brain activation when well-trained mice were required to find the goal from a novel or familiar location. Successful navigation was correlated with the activation of CA1, posterior-dorsomedial striatum, nucleus accumbens core and infralimbic cortex when allocentric-trained mice needed to use a novel route. Allocentric navigation from a familiar route activated dorsomedial striatum, nucleus accumbens, prelimbic and infralimbic cortex. None of the structures analyzed was significantly activated in egocentric-trained mice, irrespective of the starting position. These data suggest that a flexible use of stored allocentric information, that allows goal finding even from a location never explored during training, induces a shift from fronto-striatal to hippocampal circuits.

Indexed as

Nerve NetOrientation, SpatialSpatial LearningSpatial MemorySpatial NavigationAnimalsBrainMaleMiceSpace Perception

Identifiers

PMID32647258
PMCPMC7347635

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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.