Evidence map›Paper›PMID 36498900›Full record

ArticleInternational journal of molecular sciences2022

Mechanisms of Susceptibility and Resilience to PTSD: Role of Dopamine Metabolism and BDNF Expression in the Hippocampus.

Vadim E Tseilikman, Olga B Tseilikman, Anton A Pashkov, Irina S Ivleva, Marina N Karpenko, Vladislav A Shatilov, Maxim S Zhukov, Julia O Fedotova, Marina V Kondashevskaya, H Fred Downey and 1 more

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.3field-weighted citation impact, top 23% 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

8 citing papers in PubMed, 12 citations in OpenAlex.

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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

11 authors at 4 institutions in 2 countries.

Vadim E TseilikmanSchool of Medical Biology, South Ural State University, 454080 Chelyabinsk, Russia.
Olga B TseilikmanSchool of Medical Biology, South Ural State University, 454080 Chelyabinsk, Russia.
Anton A PashkovSchool of Medical Biology, South Ural State University, 454080 Chelyabinsk, Russia.
Irina S IvlevaPavlov Department of Physiology, Institute of Experimental Medicine, 197376 Saint Petersburg, Russia.ORCID 0000-0001-7659-5483
Marina N KarpenkoPavlov Department of Physiology, Institute of Experimental Medicine, 197376 Saint Petersburg, Russia.
Vladislav A ShatilovSchool of Medical Biology, South Ural State University, 454080 Chelyabinsk, Russia.
Maxim S ZhukovSchool of Medical Biology, South Ural State University, 454080 Chelyabinsk, Russia.
Julia O FedotovaLaboratory of Neuroendocrinology, Pavlov Institute of Physiology, 199034 Saint Petersburg, Russia.ORCID 0000-0002-3117-9299
Marina V KondashevskayaAvtsyn Research Institute of Human Morphology, Petrovsky National Research Center of Surgery, 117418 Moscow, Russia.ORCID 0000-0002-8096-5974
H Fred DowneySchool of Medical Biology, South Ural State University, 454080 Chelyabinsk, Russia.ORCID 0000-0002-7280-1021
Eugenia B ManukhinaSchool of Medical Biology, South Ural State University, 454080 Chelyabinsk, Russia.ORCID 0000-0002-8102-173X
South Ural State University · RUInstitute of Experimental Medicine · RUPavlov Institute of Physiology of the Russian Academy of Sciences · RUResearch Institute of Human Morphology · RU

Funding

Program for Strategic Academic Leadership Priority-2030
6 · The paper itself

Abstract

Susceptibility and resilience to post-traumatic stress disorder (PTSD) are recognized, but their mechanisms are not understood. Here, the hexobarbital sleep test (HST) was used to elucidate mechanisms of PTSD resilience or susceptibility. A HST was performed in rats 30 days prior to further experimentation. Based on the HST, the rats were divided into groups: (1) fast metabolizers (FM; sleep duration < 15 min); (2) slow metabolizers (SM; sleep duration ≥ 15 min). Then the SM and FM groups were subdivided into stressed (10 days predator scent, 15 days rest) and unstressed subgroups. Among stressed animals, only SMs developed experimental PTSD, and had higher plasma corticosterone (CORT) than stressed FMs. Thus, resilience or susceptibility to PTSD was consistent with changes in glucocorticoid metabolism. Stressed SMs had a pronounced decrease in hippocampal dopamine associated with increased expressions of catecholamine-O-methyl-transferase and DA transporter. In stressed SMs, a decrease in monoaminoxidase (MAO) A was associated with increased expressions of hippocampal MAO-A and MAO-B. BDNF gene expression was increased in stressed FMs and decreased in stressed SMs. These results demonstrate relationships between the microsomal oxidation phenotype, CORT concentration, and anxiety, and they help further the understanding of the role of the liver−brain axis during PTSD.

Indexed as

Stress Disorders, Post-TraumaticAnimalsCorticosteroneDisease Models, AnimalDopamineHexobarbitalHippocampusRatsStress, PsychologicalCorticosteroneDopamineHexobarbitalBDNFCOMTcorticosteronedopaminehexobarbital sleep testMAOpost-traumatic stress disorder

Identifiers

PMID36498900
PMCPMC9737079
OpenAlexW4309713814

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.