Evidence map›Paper›PMID 27918273›Full record

ArticleLearning & memory (Cold Spring Harbor, N.Y.)2016

Neural circuits via which single prolonged stress exposure leads to fear extinction retention deficits.

Dayan Knox, Briana R Stanfield, Jennifer M Staib, Nina P David, Samantha M Keller, Thomas DePietro

Abstract read
In one paragraph

Article in Learning & memory (Cold Spring Harbor, N.Y.), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed, 1 pooled it
–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

37 citing papers in PubMed, 1 synthesis or guideline pooled it.

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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.

Dayan KnoxDepartment of Psychological and Brain Sciences, University of Delaware, Newark, Delaware 19716, USA dknox@psych.udel.edu.
Briana R StanfieldCenter for Molecular and Behavioral Neuroscience, Rutgers University, Newark, New Jersey 07102, USA.
Jennifer M StaibDepartment of Psychological and Brain Sciences, University of Delaware, Newark, Delaware 19716, USA.
Nina P DavidSchool of Public Policy and Administration, University of Delaware, Newark, Delaware 19716, USA.
Samantha M KellerDepartment of Psychological and Brain Sciences, University of Delaware, Newark, Delaware 19716, USA.
Thomas DePietroDepartment of Psychological and Brain Sciences, University of Delaware, Newark, Delaware 19716, USA.

Funding

Predictive Modeling & Optimal Control Framework for Model-Based Epidemic Response in DelawareP20GM103446 · NIGMS · UNIVERSITY OF DELAWARE · PI MELINDA K DUNCAN · 2012 to 2026
$67.2M
Updated confocal microscope in the Imaging Core facility to support biomedical researchP20GM103653 · NIGMS · DELAWARE STATE UNIVERSITY · PI HARRINGTON, MELISSA A · 2012 to 2022
$22.7M
NIGMS NIH HHS P20 GM103446NIGMS NIH HHS P20 GM103653
6 · The paper itself

Abstract

Single prolonged stress (SPS) has been used to examine mechanisms via which stress exposure leads to post-traumatic stress disorder symptoms. SPS induces fear extinction retention deficits, but neural circuits critical for mediating these deficits are unknown. To address this gap, we examined the effect of SPS on neural activity in brain regions critical for extinction retention (i.e., fear extinction circuit). These were the ventral hippocampus (vHipp), dorsal hippocampus (dHipp), basolateral amygdala (BLA), prelimbic cortex (PL), and infralimbic cortex (IL). SPS or control rats were fear conditioned then subjected to extinction training and testing. Subsets of rats were euthanized after extinction training, extinction testing, or immediate removal from the housing colony (baseline condition) to assay c-Fos levels (measure of neural activity) in respective brain region. SPS induced extinction retention deficits. During extinction training SPS disrupted enhanced IL neural activity and inhibited BLA neural activity. SPS also disrupted inhibited BLA and vHipp neural activity during extinction testing. Statistical analyses suggested that SPS disrupted functional connectivity within the dHipp during extinction training and increased functional connectivity between the BLA and vHipp during extinction testing. Our findings suggest that SPS induces extinction retention deficits by disrupting both excitatory and inhibitory changes in neural activity within the fear extinction circuit and inducing changes in functional connectivity within the Hipp and BLA.

Indexed as

AmygdalaAnimalsCerebral CortexElectroshockExtinction, PsychologicalFactor Analysis, StatisticalFearFreezing Reaction, CatalepticHippocampusImmunohistochemistryMaleMemory DisordersNeural PathwaysNeuronsProto-Oncogene Proteins c-fosRats, Sprague-DawleyProto-Oncogene Proteins c-fos

Identifiers

PMID27918273
PMCPMC5110987

What OpenQuestion holds

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Registered trials

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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.