Evidence map›Paper›PMID 37015224›Full record

ArticleNeuron2023

Emergence of a predictive model in the hippocampus.

Adam M P Miller, Alex D Jacob, Adam I Ramsaran, Mitchell L De Snoo, Sheena A Josselyn, Paul W Frankland

Abstract read
In one paragraph

Article in Neuron, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Article
  2. Article
  3. The Cognitive-Affective Social Processing and Emotion Regulation (CASPER) model.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2026
    Review
  4. dCA1 cells encode and update contextual place preference.Frontiers in systems neuroscience · 2026
    Article
  5. Article
  6. Article
  7. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors.

Adam M P MillerProgram in Neurosciences and Mental Health, The Hospital for Sick Children, Toronto, ON, Canada.
Alex D JacobProgram in Neurosciences and Mental Health, The Hospital for Sick Children, Toronto, ON, Canada; Department of Psychology, University of Toronto, Toronto, ON, Canada.
Adam I RamsaranProgram in Neurosciences and Mental Health, The Hospital for Sick Children, Toronto, ON, Canada; Department of Psychology, University of Toronto, Toronto, ON, Canada.
Mitchell L De SnooProgram in Neurosciences and Mental Health, The Hospital for Sick Children, Toronto, ON, Canada; Institute of Medical Sciences, University of Toronto, Toronto, ON, Canada.
Sheena A JosselynProgram in Neurosciences and Mental Health, The Hospital for Sick Children, Toronto, ON, Canada; Department of Psychology, University of Toronto, Toronto, ON, Canada; Department of Physiology, University of Toronto, Toronto, ON, Canada; Institute of Medical Sciences, University of Toronto, Toronto, ON, Canada; Brain, Mind, & Consciousness Program, Canadian Institute for Advanced Research, Toronto, ON, Canada.
Paul W FranklandProgram in Neurosciences and Mental Health, The Hospital for Sick Children, Toronto, ON, Canada; Department of Psychology, University of Toronto, Toronto, ON, Canada; Department of Physiology, University of Toronto, Toronto, ON, Canada; Institute of Medical Sciences, University of Toronto, Toronto, ON, Canada; Child & Brain Development Program, Canadian Institute for Advanced Research, Toronto, ON, Canada. Electronic address: paul.frankland@sickkids.ca.

Funding

The Role of Neuronal Ensembles Supporting Auditory Fear Conditioning (Engrams) in the Amygdala in Memory Formation, Generalization and ExtinctionR01MH119421 · NIMH · HOSPITAL FOR SICK CHLDRN (TORONTO) · PI FRANKLAND, PAUL, JOSSELYN, SHEENA A · 2019 to 2023
$1.7M
Developmental Regulation of Memory Specificity by the Brain Extracellular MatrixF31MH120920 · NIMH · UNIVERSITY OF TORONTO · PI RAMSARAN, ADAM I · 2019 to 2020
$66k
NIMH NIH HHS F31 MH120920NIMH NIH HHS R01 MH119421
6 · The paper itself

Abstract

The brain organizes experiences into memories that guide future behavior. Hippocampal CA1 population activity is hypothesized to reflect predictive models that contain information about future events, but little is known about how they develop. We trained mice on a series of problems with or without a common statistical structure to observe how memories are formed and updated. Mice that learned structured problems integrated their experiences into a predictive model that contained the solutions to upcoming novel problems. Retrieving the model during learning improved discrimination accuracy and facilitated learning. Using calcium imaging to track CA1 activity during learning, we found that hippocampal ensemble activity became more stable as mice formed a predictive model. The hippocampal ensemble was reactivated during training and incorporated new activity patterns from each training problem. These results show how hippocampal activity supports building predictive models by organizing new information with respect to existing memories.

Indexed as

HippocampusLearningAnimalsCalciumMiceCalciumcontexthippocampusinferenceintegrationlatent statelearningmemorypredictionretrievalschema

Identifiers

PMID37015224
PMCPMC10293047

What OpenQuestion holds

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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.