Evidence map›Paper›PMID 27762270›Full record

ArticleNeuropsychopharmacology : official publication of the American College of Neuropsychopharmacology2017

β-Adrenergic Receptors Regulate the Acquisition and Consolidation Phases of Aversive Memory Formation Through Distinct, Temporally Regulated Signaling Pathways.

Hillary C Schiff, Joshua P Johansen, Mian Hou, David E A Bush, Emily K Smith, JoAnna E Klein, Joseph E LeDoux, Robert M Sears

Open access · bronzeAbstract read
In one paragraph

Article in Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
4.5field-weighted citation impact, top 5% 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

42 citing papers in PubMed, 71 citations in OpenAlex.

  1. Review
  2. Locus coeruleus-amygdala circuit disrupts prefrontal control to impair fear extinction.Proceedings of the National Academy of Sciences of the United States of America · 2026
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  12. Mutant βProceedings of the National Academy of Sciences of the United States of America · 2023
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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

8 authors at 3 institutions in 2 countries.

Hillary C SchiffCenter for Neural Science, New York University, New York, NY, USA.
Joshua P JohansenRIKEN Brain Science Institute, Laboratory for Neural Circuitry of Memory, Wako-shi, Saitama, Japan.
Mian HouCenter for Neural Science, New York University, New York, NY, USA.
David E A BushCenter for Neural Science, New York University, New York, NY, USA.
Emily K SmithCenter for Neural Science, New York University, New York, NY, USA.
JoAnna E KleinCenter for Neural Science, New York University, New York, NY, USA.
Joseph E LeDouxCenter for Neural Science, New York University, New York, NY, USA.
Robert M SearsCenter for Neural Science, New York University, New York, NY, USA.ORCID http://orcid.org/0000-0001-5688-1853
New York University · USNathan Kline Institute for Psychiatric Research · USTokyo University of the Arts · JP

Funding

SYNAPTIC TRANSMISSION IN FEAR CONDITIONING CIRCUITSR01MH046516 · NIMH · NEW YORK UNIVERSITY · PI LEDOUX, JOSEPH E · 1991 to 2015
$5.3M
NIMH NIH HHS R01 MH046516
6 · The paper itself

Abstract

Memory formation requires the temporal coordination of molecular events and cellular processes following a learned event. During Pavlovian threat (fear) conditioning (PTC), sensory and neuromodulatory inputs converge on post-synaptic neurons within the lateral nucleus of the amygdala (LA). By activating an intracellular cascade of signaling molecules, these G-protein-coupled neuromodulatory receptors are capable of recruiting a diverse profile of plasticity-related proteins. Here we report that norepinephrine, through its actions on β-adrenergic receptors (βARs), modulates aversive memory formation following PTC through two molecularly and temporally distinct signaling mechanisms. Specifically, using behavioral pharmacology and biochemistry in adult rats, we determined that βAR activity during, but not after PTC training initiates the activation of two plasticity-related targets: AMPA receptors (AMPARs) for memory acquisition and short-term memory and extracellular regulated kinase (ERK) for consolidating the learned association into a long-term memory. These findings reveal that βAR activity during, but not following PTC sets in motion cascading molecular events for the acquisition (AMPARs) and subsequent consolidation (ERK) of learned associations.

Indexed as

AnimalsBasolateral Nuclear ComplexBehavior, AnimalConditioning, ClassicalExtracellular Signal-Regulated MAP KinasesFearMaleMAP Kinase Signaling SystemMemoryNorepinephrineRatsRats, Sprague-DawleyReceptors, Adrenergic, betaReceptors, AMPASignal TransductionExtracellular Signal-Regulated MAP KinasesNorepinephrineReceptors, Adrenergic, betaReceptors, AMPA

Identifiers

PMID27762270
PMCPMC5312069
OpenAlexW2534155835

What OpenQuestion holds

Textmetadata
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.