Evidence map›Paper›PMID 40189005›Full record

ReviewBiological psychiatry2025

Integrating Aversive Memories in the Basolateral Amygdala.

Jianfeng Liu, Michael S Totty, Hugo Bayer, Stephen Maren

Abstract readReview
In one paragraph

Review in Biological 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. 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

4 authors.

Jianfeng LiuCollege of Life Sciences and Health, Wuhan University of Science and Technology, Wuhan, China; School of Medicine, Wuhan University of Science and Technology, Wuhan, China. Electronic address: liujianfeng@wust.edu.cn.
Michael S TottyDepartment of Biostatistics, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland.
Hugo BayerDepartment of Psychological and Brain Sciences, Texas A&M University, College Station, Texas; Institute for Neuroscience, Texas A&M University, College Station, Texas.
Stephen MarenDepartment of Psychology, University of Illinois Urbana-Champaign, Champaign, Illinois; Neuroscience Graduate Program, University of Illinois Urbana-Champaign, Urbana, Illinois; Beckman Institute for Advanced Science and Technology, University of Illinois Urbana-Champaign, Urbana, Illinois. Electronic address: smaren@illinois.edu.

Funding

Neural Substrates of Contextual Memory in Fear ExtinctionR01MH065961 · NIMH · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI MAREN, STEPHEN · 2003 to 2025
$7.9M
Neural Circuits for Stress-Impaired Extinction LearningR01MH117852 · NIMH · UNIVERSITY OF ILLINOIS AT URBANA-CHAMPAIGN · PI Stephen Maren · 2018 to 2026
$4.6M
NIMH NIH HHS R01 MH065961NIMH NIH HHS R01 MH117852
6 · The paper itself

Abstract

Decades of research have established a critical role of the basolateral complex of the amygdala (BLA) in the encoding and storage of aversive memories. Much of this work has utilized Pavlovian fear conditioning procedures in which animals experience a single aversive event. Although this effort has produced great insight into the neural mechanisms that support fear memories for an isolated aversive experience, much less is known about how amygdala circuits encode and integrate multiple emotional experiences. The emergence of methods to label and record neuronal ensembles over days allows a deeper understanding of how amygdala neurons encode and integrate distinct aversive episodes over time. Here, we review evidence that the BLA is an essential site for the persistent storage of long-term fear memory. As a long-term storage site for fear memory, a challenge for encoding multiple fear memories is the mechanisms by which BLA neurons allocate, integrate, and discriminate distinct experiences from one another. In this review, we discuss the historical evidence supporting the BLA as a critical site for long-term memory storage, as well as new evidence that stems from technological advances that allow researchers to simultaneously study the encoding and storage of multiple memory traces, including recent versus remote experiences. We explore the possibility that dysfunction in ensemble coding schemes contributes to the pathophysiology of posttraumatic stress disorder and argue that future studies should place increased emphasis on potential subregional differences in memory coding schemes in the amygdala to deepen our understanding of both normal and pathological emotional memory.

Indexed as

Basolateral Nuclear ComplexFearMemoryMemory, Long-TermAmygdalaAnimalsConditioning, ClassicalHumansNeuronsAversive conditioningBasolateral amygdalaEngramPTSDRemote fear memory

Identifiers

PMID40189005
PMCPMC13198162

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.