Evidence map›Paper›PMID 36056107›Full record

ArticleNeuropsychopharmacology : official publication of the American College of Neuropsychopharmacology2023

Basal forebrain cholinergic signaling in the basolateral amygdala promotes strength and durability of fear memories.

Byron E Crimmins, Nura W Lingawi, Billy C Chieng, Beatrice K Leung, Stephen Maren, Vincent Laurent

Open access · hybridAbstract read
In one paragraph

Article in Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
4.8field-weighted citation impact, top 4% 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

27 citing papers in PubMed, 43 citations in OpenAlex.

  1. Article
  2. Article
  3. The cholinergic basal forebrain and its role in neurodegeneration.Journal of neuropathology and experimental neurology · 2025
    Review
  4. Article
  5. Article
  6. Article
  7. Infralimbic Projections to the Substantia Innominata-Ventral Pallidum Constrain Defensive Behavior during Extinction Learning.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2025
    Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Histamine HNature communications · 2024
    Article
  15. Article
  16. Article
  17. Review
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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 2 institutions in 2 countries.

Byron E CrimminsDecision Neuroscience Laboratory, School of Psychology, University of New South Wales, Sydney, NSW, Australia.
Nura W LingawiDecision Neuroscience Laboratory, School of Psychology, University of New South Wales, Sydney, NSW, Australia.
Billy C ChiengDecision Neuroscience Laboratory, School of Psychology, University of New South Wales, Sydney, NSW, Australia.ORCID 0000-0003-0222-8001
Beatrice K LeungDecision Neuroscience Laboratory, School of Psychology, University of New South Wales, Sydney, NSW, Australia.
Stephen MarenDepartment of Psychological and Brain Sciences and Institute for Neuroscience, Texas A&M University, College Station, TX, USA.ORCID 0000-0002-9342-7411
Vincent LaurentDecision Neuroscience Laboratory, School of Psychology, University of New South Wales, Sydney, NSW, Australia. v.laurent@unsw.edu.au.ORCID 0000-0003-2333-8437
UNSW Sydney · AUTexas A&M University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The basolateral amygdala (BLA) complex receives dense cholinergic projections from the nucleus basalis of Meynert (NBM) and the horizontal limb of the diagonal band of Broca (HDB). The present experiments examined whether these projections regulate the formation, extinction, and renewal of fear memories. This was achieved by employing a Pavlovian fear conditioning protocol and optogenetics in transgenic rats. Silencing NBM projections during fear conditioning weakened the fear memory produced by that conditioning and abolished its renewal after extinction. By contrast, silencing HDB projections during fear conditioning had no effect. Silencing NBM or HDB projections during extinction enhanced the loss of fear produced by extinction, but only HDB silencing prevented renewal. Next, we found that systemic blockade of nicotinic acetylcholine receptors during fear conditioning mimicked the effects produced by silencing NBM projections during fear conditioning. However, this blockade had no effect when given during extinction. These findings indicate that basal forebrain cholinergic signaling in the BLA plays a critical role in fear regulation by promoting strength and durability of fear memories. We concluded that cholinergic compounds may improve treatments for post-traumatic stress disorder by durably stripping fear memories from their fear-eliciting capacity.

Indexed as

Basal ForebrainBasolateral Nuclear ComplexAnimalsCholinergic AgentsConditioning, ClassicalExtinction, PsychologicalFearRatsCholinergic Agents

Identifiers

PMID36056107
PMCPMC9938249
OpenAlexW4294316901

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.