Evidence map›Paper›PMID 27525673›Full record

ArticleMolecular neurobiology2017

Chronic Postnatal Stress Induces Depressive-like Behavior in Male Mice and Programs second-Hit Stress-Induced Gene Expression Patterns of OxtR and AvpR1a in Adulthood.

Alexandra Lesse, Kathy Rether, Nicole Gröger, Katharina Braun, Jörg Bock

Abstract read
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In one paragraph

Article in Molecular neurobiology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
10.3field-weighted citation impact, top 2% 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

36 citing papers in PubMed, 61 citations in OpenAlex.

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  8. Intertwined associations between oxytocin, immune system and major depressive disorder.Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie · 2023
    Review
  9. Roles of the Oxytocin Receptor (OXTR) in Human Diseases.International journal of molecular sciences · 2023
    Review
  10. Article
  11. Article
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  14. Article
  15. Epigenetic Modulation of Vasopressin Expression in Health and Disease.International journal of molecular sciences · 2021
    Review
  16. Article
  17. Article
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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 2 institutions in 1 country.

Alexandra LesseDepartment of Zoology and Developmental Neurobiology, Institute of Biology, Otto von Guericke University, Magdeburg, Germany.
Kathy RetherDepartment of Zoology and Developmental Neurobiology, Institute of Biology, Otto von Guericke University, Magdeburg, Germany.
Nicole GrögerDepartment of Zoology and Developmental Neurobiology, Institute of Biology, Otto von Guericke University, Magdeburg, Germany.
Katharina BraunDepartment of Zoology and Developmental Neurobiology, Institute of Biology, Otto von Guericke University, Magdeburg, Germany.
Jörg BockDepartment of Zoology and Developmental Neurobiology, Institute of Biology, Otto von Guericke University, Magdeburg, Germany. joerg.bock@ovgu.de.
Otto-von-Guericke University Magdeburg · DECenter for Behavioral Brain Sciences · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chronic stress (CS) during early life represents a major risk factor for the development of mental disorders, including depression. According to the Two/Multiple-Hit hypothesis, the etiology of neuropsychiatric disorders usually involves multiple stressors experienced subsequently during different phases of life. However, the molecular and cellular mechanisms modulating neuronal and behavioral changes induced by multiple stress experiences are just poorly understood. Since the oxytocinergic and vasopressinergic systems are neuroendocrine modulators involved in environmentally driven adaptations of stress sensitivity we hypothesized that postnatal CS programs oxytocinergic and vasopressinergic receptor expression changes in response to a second stress exposure in young adulthood. First we investigated if postnatal CS (maternal separation + social isolation) induces depressive-like behavior and alters oxytocin receptor (OxtR) and arginine vasopressin receptor type 1a (AvpR1a) gene expression in the hippocampus (HC) of male mice and (2) if a second single stressor (forced swimming, FS) in young adulthood affects gene expression of OxtR and AvpR1a at adulthood dependent on CS pre-experience. We found that postnatal CS induced depressive-like behavior and enhanced AvpR1a expression in HC at young adulthood. Moreover, in line with our hypothesis, only combined stress exposure (CS + FS), but not CS or FS alone, resulted in increased gene expression of OxtR in HC at adulthood. In contrast, AvpR1a expression was decreased in both adult FS and CS + FS animals. Overall, our results provide evidence that CS programs neuroendocrine systems and thereby influences stress responses in later life periods.

Indexed as

Behavior, AnimalGene Expression RegulationAgingAnimalsAnimals, NewbornChoice BehaviorChronic DiseaseDepressionHippocampusMaleMaternal DeprivationMice, Inbred C57BLReceptors, OxytocinReceptors, VasopressinSocial IsolationStress, PsychologicalReceptors, OxytocinReceptors, VasopressinDepressionEarly-life stressLimbicNeuropeptideTwo-hit

Identifiers

PMID27525673
OpenAlexW2515708380

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.