Evidence map›Paper›PMID 26589802›Full record

ArticleBehavioural brain research2016

An investigation into the effects of antenatal stressors on the postpartum neuroimmune profile and depressive-like behaviors.

Caitlin K Posillico, Jaclyn M Schwarz

Abstract read
In one paragraph

Article in Behavioural brain research, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed, 1 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

27 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. [Inflammatory Biomarkers and Postpartum Depression: A Systematic Review of Literature].Canadian journal of psychiatry. Revue canadienne de psychiatrie · 2019
    Pooled it
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  11. Microglia depletion facilitates the display of maternal behavior and alters activation of the maternal brain network in nulliparous female rats.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2023
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  15. Less can be more: Fine tuning the maternal brain.Neuroscience and biobehavioral reviews · 2022
    Review
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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

2 authors.

Caitlin K PosillicoDepartment of Psychological and Brain Sciences, University of Delaware, 108 Wolf Hall, Newark, DE 19716, United States. Electronic address: ckposillico@gmail.com.
Jaclyn M SchwarzDepartment of Psychological and Brain Sciences, University of Delaware, 108 Wolf Hall, Newark, DE 19716, United States. Electronic address: jschwarz@psych.udel.edu.

Funding

Updated confocal microscope in the Imaging Core facility to support biomedical researchP20GM103653 · NIGMS · DELAWARE STATE UNIVERSITY · PI HARRINGTON, MELISSA A · 2012 to 2022
$22.7M
Sex-dependent microglial colonization and vulnerability to a neonatal infectionR21MH101663 · NIMH · UNIVERSITY OF DELAWARE · PI SCHWARZ, JACLYN MARIE · 2014 to 2015
$428k
NIGMS NIH HHS P20 GM103653NIMH NIH HHS R21 MH101663NIMH NIH HHS R21MH101663-01
6 · The paper itself

Abstract

Postpartum depression is a specific type of depression that affects approximately 10-15% of mothers [28]. While many have attributed the etiology of postpartum depression to the dramatic change in hormone levels that occurs immediately postpartum, the exact causes are not well-understood. It is well-known, however, that pregnancy induces a number of dramatic changes in the peripheral immune system that foster the development of the growing fetus. It is also well-known that changes in immune function, specifically within the brain, have been linked to several neuropsychiatric disorders including depression. Thus, we sought to determine whether pregnancy induces significant neuroimmune changes postpartum and whether stress or immune activation during pregnancy induce a unique neuroimmune profile that may be associated with depressive-like behaviors postpartum. We used late-gestation sub-chronic stress and late-gestation acute immune activation to examine the postpartum expression of depressive-like behaviors, microglial activation markers, and inflammatory cytokines within the medial prefrontal cortex (mPFC) and the hippocampus (HP). The expression of many immune molecules was significantly altered in the brain postpartum, and postpartum females also showed significant anhedonia, both independently of stress. Following late-gestation immune activation, we found a unique set of changes in neuroimmune gene expression immediately postpartum. Thus, our data indicate that even in the absence of additional stressors, postpartum females exhibit significant changes in the expression of cytokines within the brain that are associated with depressive-like behavior. Additionally, different forms of antenatal stress produce varying profiles of postpartum neuroimmune gene expression and associated depressive-like behaviors.

Indexed as

AnimalsCytokinesDepression, PostpartumDietary SucroseDrinking BehaviorFemaleHippocampusImmunohistochemistryMicrogliaPrefrontal CortexPregnancyPregnancy ComplicationsRats, Sprague-DawleyReal-Time Polymerase Chain ReactionStress, PsychologicalCytokinesDietary SucroseDepressionForced swim testImmune activationInflammationLPSMicrogliaNeuroimmunePostpartumPregnancyStress

Identifiers

PMID26589802
PMCPMC4688102

What OpenQuestion holds

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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.