Evidence map›Paper›PMID 30287193›Full record

ArticleBrain stimulation

Vagus nerve stimulation promotes generalization of conditioned fear extinction and reduces anxiety in rats.

Lindsey J Noble, Venkat B Meruva, Seth A Hays, Robert L Rennaker, Michael P Kilgard, Christa K McIntyre

Registry-linked trialAbstract read
In one paragraph

Article in Brain stimulation. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06134323 (Efficacy and Mechanism of Transcutaneous Vagus Nerve Stimulation in the Treatment of Generalized Anxiety Disorder), which is not on this map. Cited by 49 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
49citing 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.

NCT06134323 naunknown statusnot on this map

Efficacy and Mechanism of Transcutaneous Vagus Nerve Stimulation in the Treatment of Generalized Anxiety Disorder

TypeinterventionalSponsorXijing HospitalRan2023 to 2025Enrolled82ConditionsGeneralized Anxiety DisorderArmsmedication-combined transcutaneous vagus nerve stimulation, medication-combined sham stimulation
3 · Its place in the literature

Who cites it

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

  1. Pooled it
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  5. A nose-to-brain circuit underlies anxiety regulation by nasal afferent frequency in mice.Proceedings of the National Academy of Sciences of the United States of America · 2026
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  10. Therapeutic potential of slow pranayama in anxiety.Journal of family medicine and primary care · 2025
    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.

Lindsey J NobleThe University of Texas at Dallas, School of Behavior and Brain Sciences, 800 West Campbell Road, Richardson, TX, 75080-3021, United States; The University of Texas at Dallas, Texas Biomedical Device Center, 800 West Campbell Road, Richardson, TX, 75080-3021, United States.
Venkat B MeruvaThe University of Texas at Dallas, School of Behavior and Brain Sciences, 800 West Campbell Road, Richardson, TX, 75080-3021, United States.
Seth A HaysThe University of Texas at Dallas, Texas Biomedical Device Center, 800 West Campbell Road, Richardson, TX, 75080-3021, United States; The University of Texas at Dallas, Erik Jonsson School of Engineering and Computer Science, 800 West Campbell Road, Richardson, TX, 75080-3021, United States.
Robert L RennakerThe University of Texas at Dallas, School of Behavior and Brain Sciences, 800 West Campbell Road, Richardson, TX, 75080-3021, United States; The University of Texas at Dallas, Texas Biomedical Device Center, 800 West Campbell Road, Richardson, TX, 75080-3021, United States; The University of Texas at Dallas, Erik Jonsson School of Engineering and Computer Science, 800 West Campbell Road, Richardson, TX, 75080-3021, United States.
Michael P KilgardThe University of Texas at Dallas, School of Behavior and Brain Sciences, 800 West Campbell Road, Richardson, TX, 75080-3021, United States; The University of Texas at Dallas, Texas Biomedical Device Center, 800 West Campbell Road, Richardson, TX, 75080-3021, United States.
Christa K McIntyreThe University of Texas at Dallas, School of Behavior and Brain Sciences, 800 West Campbell Road, Richardson, TX, 75080-3021, United States; The University of Texas at Dallas, Texas Biomedical Device Center, 800 West Campbell Road, Richardson, TX, 75080-3021, United States. Electronic address: christa.mcintyre@utdallas.edu.

Funding

Mechanisms of Extinction of Conditioned Fear by Vagus Nerve StimulationR15MH099655 · NIMH · UNIVERSITY OF TEXAS DALLAS · PI MCINTYRE, CHRISTA · 2013 to 2013
$430k
An adjunct to prolonged exposure therapy for treating refractory PTSD patientsR43MH105014 · NIMH · MICROTRANSPONDER, INC. · PI ENGINEER, NAVZER, MCINTYRE, CHRISTA · 2016 to 2016
$224k
NIMH NIH HHS R15 MH099655NIMH NIH HHS R43 MH105014
6 · The paper itself

Abstract

backgroundExposure-based therapies are used to treat a variety of trauma- and anxiety-related disorders by generating successful extinction following cue exposure during treatment. The development of adjuvant strategies that accelerate extinction learning, improve tolerability, and increase efficiency of treatment could increase the efficacy of exposure-based therapies. Vagus nerve stimulation (VNS) paired with exposure can enhance fear extinction, in rat models of psychiatric disorders, and chronic administration of VNS reduces anxiety in rats and humans.

objectiveWe tested whether VNS, like other cognitive enhancers, could produce generalization of extinction for stimuli that are not presented during the extinction sessions, but are associated with the fear event.

methodsMale Sprague Dawley rats underwent auditory fear conditioning with two easily discriminable auditory stimuli. Following fear conditioning, extinction training consisted of exposure to only one of the conditioned sounds. Half of the rats received VNS and half received sham stimulation during with sound presentations. VNS effects on anxiety were examined in a separate study where VNS was administered prior to testing on the elevated plus maze.

resultsSham stimulated rats given 20 presentations of a conditioned stimulus (CS) during the extinction session showed performance that was matched to VNS-treated rats given only 4 presentations of the CS. Despite comparable levels of freezing to the presented CS, only the VNS-treated rats showed a significant decrease in freezing to the CS that was not presented. VNS-induced generalization of extinction was observed only when the two sounds were paired with footshock within the same fear conditioning session; VNS did not promote generalization of extinction when the two sounds were conditioned on different days or in different contexts. On the anxiety test, VNS administration significantly increased time spent in the open arms of the elevated plus maze.

conclusionThese results provide evidence that VNS can promote generalization of extinction to other stimuli associated with a specific fear experience. Furthermore, non-contingent VNS appears to reduce anxiety. The ability to generalize extinction and reduce anxiety makes VNS a potential candidate for use as an adjunctive strategy to improve the efficacy and tolerability of exposure-based therapies.

Indexed as

FearAnimalsAnxiety DisordersConditioning, ClassicalExtinction, PsychologicalMaleRatsRats, Sprague-DawleyVagus Nerve StimulationAnxietyExtinctionFearGeneralizationVagusVNS

Identifiers

PMID30287193
PMCPMC6301121

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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.