ReviewBiological psychiatry2025
Integrating Aversive Memories in the Basolateral Amygdala.
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.
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.
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.
Who cites it
3 citing papers in PubMed.
- The human amygdala in threat learning and extinction.Science advances · 2026Article
- Distinct orbitofrontal circuits with dorsal and ventral CA1 differentially regulate spatial memory and emotional behaviors.Frontiers in behavioral neuroscience · 2026Article
- Basolateral Amygdala Memory in the Fourth Dimension.Biological psychiatry · 2025Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
4 authors.
Funding
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
Identifiers
What OpenQuestion holds
Registered trials
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.