Evidence map›Paper›PMID 26944604›Full record

ArticleNeuroscience2016

Mechanisms underlying the formation of the amygdalar fear memory trace: A computational perspective.

F Feng, P Samarth, D Paré, S S Nair

Open access · greenAbstract read
In one paragraph

Article in Neuroscience, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.3field-weighted citation impact, top 13% 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

19 citing papers in PubMed, 34 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Microcircuitry and oscillation features across model cortical regions.The ... Midwest Symposium on Circuits and Systems conference proceedings : MWSCAS. Midwest Symposium on Circuits and Systems · 2025
    Article
  6. Article
  7. Article
  8. Reverse engineering information processing in lateral amygdala during auditory tones.International IEEE/EMBS Conference on Neural Engineering : [proceedings]. International IEEE EMBS Conference on Neural Engineering · 2023
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Synaptic encoding of fear memories in the amygdala.Current opinion in neurobiology · 2019
    Review
  15. Article
  16. Memory Allocation: Mechanisms and Function.Annual review of neuroscience · 2018
    Review
  17. Article
  18. Article
  19. 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 at 2 institutions in 1 country.

F FengDepartment of Electrical and Computer Engineering, University of Missouri, Columbia, MO, USA.
P SamarthDepartment of Electrical and Computer Engineering, University of Missouri, Columbia, MO, USA.
D ParéCenter for Molecular and Behavioral Neuroscience, Rutgers, The State University of New Jersey, Newark, NJ, USA.
S S NairDepartment of Electrical and Computer Engineering, University of Missouri, Columbia, MO, USA. Electronic address: nairs@missouri.edu.
University of Missouri · USRutgers, The State University of New Jersey · US

Funding

Role of intercalated amygdala neurons in the extinction of conditioned fearR01MH083710 · NIMH · RUTGERS THE STATE UNIV OF NJ NEWARK · PI PARE, DENIS · 2009 to 2013
$1.9M
CRCNS: Modeling Acquisition and Extinction of Fear Memories in Amygdala CircuitsR01MH087755 · NIMH · UNIVERSITY OF MISSOURI-COLUMBIA · PI NAIR, SATISH S · 2009 to 2011
$728k
NIMH NIH HHS MH083710NIMH NIH HHS MH087755NIMH NIH HHS R01 MH083710NIMH NIH HHS R01 MH087755
6 · The paper itself

Abstract

Recent experimental and modeling studies on the lateral amygdala (LA) have implicated intrinsic excitability and competitive synaptic interactions among principal neurons (PNs) in the formation of auditory fear memories. The present modeling studies, conducted over an expanded range of intrinsic excitability in the network, revealed that only excitable PNs that received tone inputs participate in the competition. Strikingly, the number of model PNs integrated into the fear memory trace remained constant despite the much larger range considered, and model runs highlighted several conditioning-induced tone responsive characteristics of the various PN populations. Furthermore, these studies showed that although excitation was important, disynaptic inhibition among PNs is the dominant mechanism that keeps the number of plastic PNs stable despite large variations in the network's excitability. Finally, we found that the overall level of inhibition in the model network determines the number of projection cells integrated into the fear memory trace.

Indexed as

Computer SimulationModels, NeurologicalAction PotentialsAmygdalaAnimalsCyclic AMP Response Element-Binding ProteinFearMemoryNeuronal PlasticityNeuronsCyclic AMP Response Element-Binding Proteinbiophysical modelhebbian learningsparse coding

Identifiers

PMID26944604
PMCPMC4805477
OpenAlexW2288715045

What OpenQuestion holds

Textmetadata
LicenceTDM
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.