Evidence map›Paper›PMID 33472824›Full record

ReviewThe Journal of neuroscience : the official journal of the Society for Neuroscience2021

Limbic Neuropeptidergic Modulators of Emotion and Their Therapeutic Potential for Anxiety and Post-Traumatic Stress Disorder.

Paul J Marvar, Raül Andero, Rene Hurlemann, Tiffany R Lago, Moriel Zelikowsky, Joanna Dabrowska

Open access · bronzeAbstract readReview
In one paragraph

Review in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
5.0field-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

16 citing papers in PubMed, 32 citations in OpenAlex.

  1. Trial
  2. Review
  3. Losartan treatment attenuates the cardiorenal alterations in a rat model of hemorrhagic insular stroke.Clinical autonomic research : official journal of the Clinical Autonomic Research Society · 2026
    Article
  4. Article
  5. Review
  6. Fear, anxiety, and the extended amygdala-bioRxiv : the preprint server for biology · 2025
    Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Review
  12. The Renin Angiotensin System as a Therapeutic Target in Traumatic Brain Injury.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2023
    Review
  13. Review
  14. Article
  15. Article
  16. 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

6 authors at 6 institutions in 3 countries.

Paul J MarvarDepartment of Pharmacology & Physiology, Department of Psychiatry and Behavioral Sciences, George Washington Institute for Neuroscience, George Washington University, Washington, DC, 20037.
Raül AnderoDepartament de Psicobiologia i de Metodologia de les Ciències de la Salut, Institut de Neurociències, Universitat Autònoma de Barcelona, Barcelona, Spain, 08193. Instituto de Salud Carlos III, Centro de Investigación Biomédica en Red de Salud Mental, CIBERSAM, Madrid, Spain, 28029. ICREA, Pg. Lluís Companys 23, Barcelona, Spain, 08010.
Rene HurlemannDepartment of Psychiatry, School of Medicine & Health Sciences, and Research Center Neurosensory Science, University of Oldenburg, Oldenburg, 26129, Germany.
Tiffany R LagoDepartment of Psychiatry, Veterans Administration Boston Healthcare System, Boston, Massachusetts, 02130.
Moriel ZelikowskyDepartment of Neurobiology and Anatomy, University of Utah, School of Medicine, Salt Lake City, Utah, 84112.
Joanna DabrowskaCenter for the Neurobiology of Stress Resilience and Psychiatric Disorders, Discipline of Cellular and Molecular Pharmacology, Chicago Medical School, Rosalind Franklin University of Medicine and Science, North Chicago, Illinois, 60064 joanna.dabrowska@rosalindfranklin.edu.
Carl von Ossietzky Universität Oldenburg · DEGeorge Washington University · USRosalind Franklin University of Medicine and Science · USUniversitat Autònoma de Barcelona · ESUniversity of Utah · USVA Boston Healthcare System · US

Funding

The Psychophysiology Of Fear And AnxietyZIAMH002798 · NIMH · NATIONAL INSTITUTE OF MENTAL HEALTH · PI GRILLON, CHRISTIAN · 2009 to 2022
$29.0M
The Integrated Role of Vasopressin and Oxytocin Receptors in the Modulation of BNST Activity and Fear ProcessingR01MH113007 · NIMH · ROSALIND FRANKLIN UNIV OF MEDICINE & SCI · PI Joanna Dabrowska · 2017 to 2026
$4.4M
Prefrontal Circuit Control of Isolation-Induced AggressionR01MH132822 · NIMH · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI Moriel Zelikowsky · 2023 to 2026
$2.3M
Brain Angiotensin II as a Mediator of Fear Memory and Cardiovascular DysfunctionR01HL137103 · NHLBI · GEORGE WASHINGTON UNIVERSITY · PI MARVAR, PAUL J · 2018 to 2021
$2.2M
Genetic dissection of neural circuits underlying trauma, fear, and social behaviorR00MH108734 · NIMH · UNIVERSITY OF UTAH · PI ZELIKOWSKY, MORIEL · 2019 to 2021
$747k
Intramural NIH HHS ZIA MH002798NHLBI NIH HHS R01 HL137103NIMH NIH HHS R00 MH108734NIMH NIH HHS R01 MH113007NIMH NIH HHS R01 MH132822
6 · The paper itself

Abstract

Post-traumatic stress disorder (PTSD) is characterized by hypervigilance, increased reactivity to unpredictable versus predictable threat signals, deficits in fear extinction, and an inability to discriminate between threat and safety. First-line pharmacotherapies for psychiatric disorders have limited therapeutic efficacy in PTSD. However, recent studies have advanced our understanding of the roles of several limbic neuropeptides in the regulation of defensive behaviors and in the neural processes that are disrupted in PTSD. For example, preclinical studies have shown that blockers of tachykinin pathways, such as the Tac2 pathway, attenuate fear memory consolidation in mice and thus might have unique potential as early post-trauma interventions to prevent PTSD development. Targeting this pathway might also be beneficial in regulating other symptoms of PTSD, including trauma-induced aggressive behavior. In addition, preclinical and clinical studies have shown the important role of angiotensin receptors in fear extinction and the promise of using angiotensin II receptor blockade to reduce PTSD symptom severity. Additional preclinical studies have demonstrated that the oxytocin receptors foster accurate fear discrimination by facilitating fear responses to predictable versus unpredictable threats. Complementary human imaging studies demonstrate unique neural targets of intranasal oxytocin and compare its efficacy with well-established anxiolytic treatments. Finally, promising data from human subjects have demonstrated that a selective vasopressin 1A receptor antagonist reduces anxiety induced by unpredictable threats. This review highlights these novel promising targets for the treatment of unique core elements of PTSD pathophysiology.

Indexed as

AnimalsAnxietyEmotionsExtinction, PsychologicalHumansLimbic SystemNerve NetNeuropeptidesReceptors, TachykininStress Disorders, Post-TraumaticTachykininsNeuropeptidesReceptors, TachykininTachykininsangiotensin IIanxietyoxytocinPTSDtachykininvasopressin

Identifiers

PMID33472824
PMCPMC7880296
OpenAlexW3124483349

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.