Evidence map›Paper›PMID 26830140›Full record

ArticleMolecular psychiatry2016

Maternal immune activation leads to selective functional deficits in offspring parvalbumin interneurons.

S Canetta, S Bolkan, N Padilla-Coreano, L J Song, R Sahn, N L Harrison, J A Gordon, A Brown, C Kellendonk

Open access · bronzeAbstract read
In one paragraph

Article in Molecular psychiatry, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 134 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
134citing papers in PubMed, 3 pooled it
6.3field-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

134 citing papers in PubMed, 3 syntheses or guidelines pooled it, 204 citations in OpenAlex.

  1. Pooled it
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  4. Review
  5. Article
  6. Review
  7. Article
  8. Maternal immune activation in mice recapitulates features of attention-deficit/hyperactivity disorder (ADHD) in susceptible offspring.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2026
    Article
  9. Article
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  11. Article
  12. Article
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  14. GABAFrontiers in pharmacology · 2026
    Review
  15. Review
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  19. Distinct subpopulations of parvalbumin neurons participating in divergent prefrontal functions.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2025
    Article
  20. Article

74 more citing papers are in PubMed but not listed here.

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

9 authors at 2 institutions in 1 country.

S CanettaDepartment of Psychiatry, Columbia University Medical Center, New York, NY, USA.
S BolkanDepartment of Psychiatry, Columbia University Medical Center, New York, NY, USA.
N Padilla-CoreanoDepartment of Psychiatry, Columbia University Medical Center, New York, NY, USA.
L J SongDepartment of Pharmacology, Columbia University Medical Center, New York, NY, USA.
R SahnDepartment of Psychiatry, Columbia University Medical Center, New York, NY, USA.
N L HarrisonDepartment of Pharmacology, Columbia University Medical Center, New York, NY, USA.
J A GordonDepartment of Psychiatry, Columbia University Medical Center, New York, NY, USA.
A BrownDepartment of Psychiatry, Columbia University Medical Center, New York, NY, USA.
C KellendonkDepartment of Psychiatry, Columbia University Medical Center, New York, NY, USA.
Columbia University Irving Medical Center · USNew York State Psychiatric Institute

Funding

Tumor Biology and Microenvironment ProgramP30CA013696 · NCI · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI Parisa Tehranifar · 1985 to 2026
$115.3M
Translational Research Training in Child PsychiatryT32MH016434 · NIMH · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI Cristiane S. Duarte, Kate Dimond Fitzgerald · 1985 to 2026
$10.9M
Mechanisms underlying the functional connectivity deficit in the 22q11 microdeletR01MH096274 · NIMH · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI GOGOS, JOSEPH A · 2012 to 2021
$3.6M
Prefrontal cortex and adolescent binge drinking: Role of HCN channelsR01AA023531 · NIAAA · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI HARRISON, NEIL L., SIEGELBAUM, STEVEN A · 2015 to 2019
$1.9M
Alcohol and Dopamine Release: Cellular and Synaptic MechanismsR01AA019801 · NIAAA · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI HARRISON, NEIL L., SULZER, DAVID · 2010 to 2014
$1.8M
Epidemiology of Prenatal Factors and Adult PsychopathologyK02MH065422 · NIMH · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI BROWN, ALAN STEWART · 2003 to 2012
$1.2M
Effects of maternal immune activation on offspring GABA circuitry and behaviorK01MH107760 · NIMH · NEW YORK STATE PSYCHIATRIC INSTITUTE DBA RESEARCH FOUNDATION FOR MENTAL HYGIENE, INC · PI CANETTA, SARAH E · 2016 to 2019
$732k
NCI NIH HHS P30 CA013696NIAAA NIH HHS R01 AA019801NIAAA NIH HHS R01 AA023531NIMH NIH HHS K01 MH107760NIMH NIH HHS K02 MH065422NIMH NIH HHS T32 MH016434
6 · The paper itself

Abstract

Abnormalities in prefrontal gamma aminobutyric acid (GABA)ergic transmission, particularly in fast-spiking interneurons that express parvalbumin (PV), are hypothesized to contribute to the pathophysiology of multiple psychiatric disorders, including schizophrenia, bipolar disorder, anxiety disorders and depression. While primarily histological abnormalities have been observed in patients and in animal models of psychiatric disease, evidence for abnormalities in functional neurotransmission at the level of specific interneuron populations has been lacking in animal models and is difficult to establish in human patients. Using an animal model of a psychiatric disease risk factor, prenatal maternal immune activation (MIA), we found reduced functional GABAergic transmission in the medial prefrontal cortex (mPFC) of adult MIA offspring. Decreased transmission was selective for interneurons expressing PV, resulted from a decrease in release probability and was not observed in calretinin-expressing neurons. This deficit in PV function in MIA offspring was associated with increased anxiety-like behavior and impairments in attentional set shifting, but did not affect working memory. Furthermore, cell-type specific optogenetic inhibition of mPFC PV interneurons was sufficient to impair attentional set shifting and enhance anxiety levels. Finally, we found that in vivo mPFC gamma oscillations, which are supported by PV interneuron function, were linearly correlated with the degree of anxiety displayed in adult mice, and that this correlation was disrupted in MIA offspring. These results demonstrate a selective functional vulnerability of PV interneurons to MIA, leading to affective and cognitive symptoms that have high relevance for schizophrenia and other psychiatric disorders.

Indexed as

AnimalsDisease Models, AnimalFemaleGABAergic Neuronsgamma-Aminobutyric AcidHumansImmunity, ActiveInhibition, PsychologicalInterneuronsMaleMemory, Short-TermMiceParvalbuminsPrefrontal CortexPregnancyPrenatal Exposure Delayed Effectsgamma-Aminobutyric AcidParvalbumins

Identifiers

PMID26830140
PMCPMC4914410
OpenAlexW2258502568

What OpenQuestion holds

Textmetadata
LicenceTDM
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.