Evidence map›Paper›PMID 30898126›Full record

ArticleJournal of biomedical science2019

Effects of oxytocin on prosocial behavior and the associated profiles of oxytocinergic and corticotropin-releasing hormone receptors in a rodent model of posttraumatic stress disorder.

Sheng-Chiang Wang, Chen-Cheng Lin, Nian-Sheng Tzeng, Che-Se Tung, Yia-Ping Liu

Open access · diamondAbstract read
In one paragraph

Article in Journal of biomedical science, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
4.6field-weighted citation impact, top 6% 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

19 citing papers in PubMed, 31 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

5 authors at 3 institutions in 1 country.

Sheng-Chiang WangGraduate Institute of Medical Sciences, National Defense Medical Center, No. 161, Section 6, Minquan East Road, Neihu District, Taipei City, 114, Taiwan.
Chen-Cheng LinDepartment of Psychiatry, Cheng Hsin General Hospital, No. 45, Chenghsin Street, Beitou District, Taipei City, 112, Taiwan.
Nian-Sheng TzengDepartment of Psychiatry, Tri-Service General Hospital, School of Medicine, National Defense Medical Center, No. 325, Section 2, Chenggong Road, Neihu Distict, Taipei City, 114, Taiwan.
Che-Se TungDivision of Medical Research & Education, Cheng Hsin General Hospital, No. 45, Chenghsin Street, Beitou District, Taipei City, 112, Taiwan, Republic of China.
Yia-Ping LiuGraduate Institute of Medical Sciences, National Defense Medical Center, No. 161, Section 6, Minquan East Road, Neihu District, Taipei City, 114, Taiwan. yiaping@mail.ndmctsgh.edu.tw.ORCID http://orcid.org/0000-0002-1171-6560
Cheng Hsin General Hospital · TWTri-Service General Hospital · TWTri-Service General Hospital Songshan Branch · TW

Funding

Ministry of Science and Technology, Taiwan MOST 104-2410-H-016-001, 105-2410-H-016-002-MY2National Defense Medical Center (TW) MAB-104-007, MAB-106-022, and MAB-106-023Tri-Service General Hospital (TW) Songshan Branch 104-03, 105-06, 106-06
6 · The paper itself

Abstract

backgroundTraumatic experience may lead to various psychological sequelae including the unforgettable trauma-associated memory as seen in posttraumatic stress disorder (PTSD), with a mechanism of impaired fear extinction due to biological imbalance among hypothalamic-pituitary-adrenal (HPA) axis and fear circuit areas such as medial prefrontal cortex (mPFC), hippocampus, and amygdala. Recently the impaired sociability seen in PTSD patients received great attention and the involvement of oxytocin (OXT) mediation is worth being investigated. This study examined whether the trauma-altered prosocial behavior can be modulated by OXT manipulation and its relationship with corticotropin-releasing hormone (CRH) signaling.

methodsMale rats previously exposed to a single prolonged stress (SPS) were evaluated for their performance in social choice test (SCT) and novel object recognition test (NORT) following the introduction of intranasal oxytocin (OXT) and OXT receptor antagonist atosiban (ASB). OXT receptors (OXTR) and CRH receptors (CRHR1, CRHR2) were quantified in both protein and mRNA levels in medial prefrontal cortex (mPFC), hippocampus, and amygdala.

resultsSPS reduced inclination of rats staying at the sociable place with performing less prosocial contacts. OXT can amend the deficit but this effect was blocked by ASB. Expression of OXTR became reduced following SPS in mPFC and amygdala, the latter exhibited higher therapeutic specificity to OXT. Expression of CRHR1 appeared more sensitive than CRHR2 to SPS, higher CRHR1 protein levels were found in mPFC and amygdala.

conclusionPsychological trauma-impaired sociability is highly associated with OXT signaling pathway. Intranasal OXT restored both the SPS-impaired prosocial contacts and the SPS-reduced OXTR expressions in mPFC and amygdala. OXT may have therapeutic potential to treat PTSD patients with impaired social behaviors.

Indexed as

Social BehaviorAdministration, IntranasalAnimalsCRF Receptor, Type 1Gene ExpressionHormone AntagonistsHumansMaleOxytocicsOxytocinRatsRats, Sprague-DawleyReceptors, Corticotropin-Releasing HormoneReceptors, OxytocinSignal TransductionStress Disorders, Post-TraumaticatosibanCRF Receptor, Type 1CRF receptor type 2Hormone AntagonistsOxytocicsOxytocinoxytocin receptor, ratReceptors, Corticotropin-Releasing HormoneReceptors, OxytocinVasotocinCorticotropin-releasing hormoneFear circuit areasOxytocinPosttraumatic stress disorder, Prosocial behavior, Single prolonged stress.

Identifiers

PMID30898126
PMCPMC6427848
OpenAlexW2938538365

What OpenQuestion holds

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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 OpenQuestion graph.