Evidence map›Paper›PMID 39728686›Full record

ReviewPathophysiology : the official journal of the International Society for Pathophysiology2024

Rat Models in Post-Traumatic Stress Disorder Research: Strengths, Limitations, and Implications for Translational Studies.

Alexey Sarapultsev, Maria Komelkova, Oleg Lookin, Sergey Khatsko, Evgenii Gusev, Alexander Trofimov, Tursonjan Tokay, Desheng Hu

Abstract readReview
In one paragraph

Review in Pathophysiology : the official journal of the International Society for Pathophysiology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
–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

12 citing papers in PubMed.

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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.

Alexey SarapultsevInstitute of Immunology and Physiology, Ural Branch of the Russian Academy of Science, 106 Pervomaiskaya Street, 620049 Ekaterinburg, Russia.ORCID 0000-0003-3101-9655
Maria KomelkovaRussian-Chinese Education and Research Center of System Pathology, South Ural State University, 76 Lenin Prospekt, 454080 Chelyabinsk, Russia.ORCID 0000-0003-2431-8358
Oleg LookinNational Scientific Medical Center, Astana 010000, Kazakhstan.ORCID 0000-0001-9544-1885
Sergey KhatskoAnatomical and Physiological Experimental Laboratory, Department of Experimental Biology and Biotechnology, Institute of Natural Sciences and Mathematics, 48 Kuybysheva Str., 620026 Ekaterinburg, Russia.ORCID 0000-0001-5921-6680
Evgenii GusevInstitute of Immunology and Physiology, Ural Branch of the Russian Academy of Science, 106 Pervomaiskaya Street, 620049 Ekaterinburg, Russia.ORCID 0000-0002-7145-2376
Alexander TrofimovBiology Department, School of Sciences and Humanities, Nazarbayev University, 53 Kabanbai Batyr Ave., Astana 010000, Kazakhstan.ORCID 0000-0001-6745-6035
Tursonjan TokayBiology Department, School of Sciences and Humanities, Nazarbayev University, 53 Kabanbai Batyr Ave., Astana 010000, Kazakhstan.ORCID 0000-0003-2219-3301
Desheng HuDepartment of Integrated Traditional Chinese and Western Medicine, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430000, China.

Funding

Institute of Immunology and Physiology 122020900136-4South Ural State University FENU-2023-0014
6 · The paper itself

Abstract

Post-Traumatic Stress Disorder (PTSD) is a multifaceted psychiatric disorder triggered by traumatic events, leading to prolonged psychological distress and varied symptoms. Rat models have been extensively used to explore the biological, behavioral, and neurochemical underpinnings of PTSD. This review critically examines the strengths and limitations of commonly used rat models, such as single prolonged stress (SPS), stress-re-stress (S-R), and predator-based paradigms, in replicating human PTSD pathology. While these models provide valuable insights into neuroendocrine responses, genetic predispositions, and potential therapeutic targets, they face challenges in capturing the full complexity of PTSD, particularly in terms of ethological relevance and translational validity. We assess the degree to which these models mimic the neurobiological and behavioral aspects of human PTSD, highlighting areas where they succeed and where they fall short. This review also discusses future directions in refining these models to improve their utility for translational research, aiming to bridge the gap between preclinical findings and clinical applications.

Indexed as

ethological validitymodel limitationsneuroendocrine factorspharmacological interventionsPTSDratsrodent modelssingle prolonged stress (SPS)stress–re-stress paradigmtranslational research

Identifiers

PMID39728686
PMCPMC11679995

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.