Evidence map›Paper›PMID 29867615›Full record

ReviewFrontiers in psychiatry2018

Single-Prolonged Stress: A Review of Two Decades of Progress in a Rodent Model of Post-traumatic Stress Disorder.

Michael J Lisieski, Andrew L Eagle, Alana C Conti, Israel Liberzon, Shane A Perrine

Abstract readReview
In one paragraph

Review in Frontiers in psychiatry, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 123 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
123citing papers in PubMed, 2 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

123 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
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  12. D[HisPsychopharmacology · 2026
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  20. Modulating Role of Resveratrol in Metabolic and Inflammatory Dysregulation Caused by Surgical and Psychoemotional Stress in Rats.Pathophysiology : the official journal of the International Society for Pathophysiology · 2025
    Article

63 more citing papers are in PubMed but not listed here.

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

5 authors.

Michael J LisieskiDepartment of Psychiatry and Behavioral Neurosciences, Wayne State University School of Medicine, Detroit, MI, United States.
Andrew L EagleDepartment of Physiology, Michigan State University, East Lansing, MI, United States.
Alana C ContiResearch and Development Service, John D. Dingell Veterans Affairs Medical Center, Detroit, MI, United States.
Israel LiberzonDepartment of Psychiatry, University of Michigan, Ann Arbor, MI, United States.
Shane A PerrineDepartment of Psychiatry and Behavioral Neurosciences, Wayne State University School of Medicine, Detroit, MI, United States.

Funding

Effects of cocaine taking and seeking on histone deacetylase class IIa enzyme activity in the nucleus accumbens of ratsR01DA042057 · NIDA · WAYNE STATE UNIVERSITY · PI PERRINE, SHANE ALAN · 2017 to 2021
$3.0M
Longitudinal Assessment of Cortical Hypoactivity in a Model of Comorbid TBI-PTSDI01RX001511 · VA · JOHN D DINGELL VA MEDICAL CENTER · PI CONTI, ALANA C. · 2015 to 2019
–
Cannabinoids for Posttraumatic Stress Disorder and Alcohol UseI01RX002252 · VA · JOHN D DINGELL VA MEDICAL CENTER · PI PERRINE, SHANE ALAN · 2018 to 2021
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NIDA NIH HHS R01 DA042057RRD VA I01 RX001511RRD VA I01 RX002252
6 · The paper itself

Abstract

Post-traumatic stress disorder (PTSD) is a common, costly, and often debilitating psychiatric condition. However, the biological mechanisms underlying this disease are still largely unknown or poorly understood. Considerable evidence indicates that PTSD results from dysfunction in highly-conserved brain systems involved in stress, anxiety, fear, and reward. Pre-clinical models of traumatic stress exposure are critical in defining the neurobiological mechanisms of PTSD, which will ultimately aid in the development of new treatments for PTSD. Single prolonged stress (SPS) is a pre-clinical model that displays behavioral, molecular, and physiological alterations that recapitulate many of the same alterations observed in PTSD, illustrating its validity and giving it utility as a model for investigating post-traumatic adaptations and pre-trauma risk and protective factors. In this manuscript, we review the present state of research using the SPS model, with the goals of (1) describing the utility of the SPS model as a tool for investigating post-trauma adaptations, (2) relating findings using the SPS model to findings in patients with PTSD, and (3) indicating research gaps and strategies to address them in order to improve our understanding of the pathophysiology of PTSD.

Indexed as

amygdalaanxietyhippocampusHPA axispre-clinical modelsprefrontal cortexPTSDsingle prolonged stress

Identifiers

PMID29867615
PMCPMC5962709

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.