Evidence map›Paper›PMID 36977579›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2023

Goal Choices Modify Frontotemporal Memory Representations.

Aditya Srinivasan, Justin S Riceberg, Michael R Goodman, Arvind Srinivasan, Kevin G Guise, Matthew L Shapiro

Open access · greenAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2023. 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
0.5field-weighted citation impact, top 38% 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

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. The Ubiquity of Time in Latent-cause Inference.Journal of cognitive neuroscience · 2024
    Article
  2. Article
  3. 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

6 authors at 3 institutions in 1 country.

Aditya SrinivasanDepartment of Neuroscience and Experimental Therapeutics, Albany Medical College, Albany, New York 12208 sriniva1@amc.edu shapirm@amc.edu.
Justin S RicebergDepartment of Neuroscience and Experimental Therapeutics, Albany Medical College, Albany, New York 12208.ORCID 0000-0002-7046-1502
Michael R GoodmanDepartment of Neuroscience and Experimental Therapeutics, Albany Medical College, Albany, New York 12208.
Arvind SrinivasanCollege of Health Sciences, California Northstate University, Rancho Cordova, California 95670.
Kevin G GuiseFriedman Brain Institute, Leon and Norma Hess Center for Science and Medicine, Icahn School of Medicine at Mount Sinai, New York, New York 10029.
Matthew L ShapiroDepartment of Neuroscience and Experimental Therapeutics, Albany Medical College, Albany, New York 12208 sriniva1@amc.edu shapirm@amc.edu.
Albany Medical Center Hospital · USCalifornia Northstate University · USAllen Institute for Brain Science · US

Funding

Prospective memory coding by the hippocampusR01MH073689 · NIMH · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI SHAPIRO, MATTHEW L · 2006 to 2022
$5.7M
Maturation of frontal cortico-thalamic circuitry in control of social behaviorR01MH118297 · NIMH · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI Hirofumi Morishita · 2019 to 2026
$4.6M
Mechanisms regulating the maturation of prefrontal top-down circuity in control of attentional behaviorR01MH119523 · NIMH · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI MORISHITA, HIROFUMI · 2019 to 2023
$3.2M
NIMH NIH HHS R01 MH073689NIMH NIH HHS R01 MH118297NIMH NIH HHS R01 MH119523
6 · The paper itself

Abstract

Adapting flexibly to changing circumstances is guided by memory of past choices, their outcomes in similar circumstances, and a method for choosing among potential actions. The hippocampus (HPC) is needed to remember episodes, and the prefrontal cortex (PFC) helps guide memory retrieval. Single-unit activity in the HPC and PFC correlates with such cognitive functions. Previous work recorded CA1 and mPFC activity as male rats performed a spatial reversal task in a plus maze that requires both structures, found that PFC activity helps reactivate HPC representations of pending goal choices but did not describe frontotemporal interactions after choices. We describe these interactions after choices here. CA1 activity tracked both current goal location and the past starting location of single trials; PFC activity tracked current goal location better than past start location. CA1 and PFC reciprocally modulated representations of each other both before and after goal choices. After choices, CA1 activity predicted changes in PFC activity in subsequent trials, and the magnitude of this prediction correlated with faster learning. In contrast, PFC start arm activity more strongly modulated CA1 activity after choices correlated with slower learning. Together, the results suggest post-choice HPC activity conveys retrospective signals to the PFC, which combines different paths to common goals into rules. In subsequent trials, prechoice mPFC activity modulates prospective CA1 signals informing goal selection.

Indexed as

GoalsHippocampusAnimalsMaleMaze LearningPrefrontal CortexProspective StudiesRatsRetrospective StudiesCA1learningmPFC

Identifiers

PMID36977579
PMCPMC10162456
OpenAlexW4361019776

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.