Evidence map›Paper›PMID 31712551›Full record

ArticleTranslational psychiatry2019

Prefrontal cortex interneurons display dynamic sex-specific stress-induced transcriptomes.

Matthew J Girgenti, Eric S Wohleb, Sameet Mehta, Sriparna Ghosal, Manoela V Fogaca, Ronald S Duman

Open access · goldAbstract read
In one paragraph

Article in Translational psychiatry, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
3.4field-weighted citation impact, top 7% 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

34 citing papers in PubMed, 53 citations in OpenAlex.

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  17. Tianeptine promotes lasting antiallodynic effects in a mouse model of neuropathic pain.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2023
    Article
  18. Article
  19. Plasticity of synapses and reward circuit function in the genesis and treatment of depression.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2023
    Review
  20. Article
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

6 authors at 1 institution in 1 country.

Matthew J GirgentiDepartment of Psychiatry, Yale University School of Medicine, 34 Park Street, New Haven, CT, 06520, USA.ORCID http://orcid.org/0000-0003-1647-326X
Eric S WohlebDepartment of Psychiatry, Yale University School of Medicine, 34 Park Street, New Haven, CT, 06520, USA.
Sameet MehtaYale Center for Genome Analysis, Yale University School of Medicine, New Haven, CT, 06520, USA.
Sriparna GhosalDepartment of Psychiatry, Yale University School of Medicine, 34 Park Street, New Haven, CT, 06520, USA.
Manoela V FogacaDepartment of Psychiatry, Yale University School of Medicine, 34 Park Street, New Haven, CT, 06520, USA.
Ronald S DumanDepartment of Psychiatry, Yale University School of Medicine, 34 Park Street, New Haven, CT, 06520, USA. ronald.duman@yale.edu.
Yale University · US

Funding

Synaptic mechanisms underlying the rapid antidepressant actions of scopolamineR01MH105910 · NIMH · YALE UNIVERSITY · PI PICCIOTTO, MARINA R · 2014 to 2018
$2.2M
High Performance Computing Instrumentation for the Yale Center for Genome AnalysiS10OD018521 · OD · YALE UNIVERSITY · PI MANE, SHRIKANT M · 2015 to 2015
$890k
NIH HHS S10 OD018521U.S. Department of Health & Human Services | NIH | National Institute of Mental Health (NIMH) MH105910
6 · The paper itself

Abstract

γ-aminobutyric acid (GABA) inhibitory interneurons play a key role in efferent and afferent control of principle neuron activity in the prefrontal cortex (PFC), thereby regulating signal integrity of cognitive and behavioral processes. Recent evidence suggests that specific subtypes of interneurons in the PFC mediate stress-induced depressive-like behaviors. Abnormalities of GABA interneurons, particularly the somatostatin (human, SST; mouse, Sst) subtype, have been reported in postmortem brains of depressed subjects and include sex differences that could explain the increased incidence of depression in women. Here, we analyze the transcriptional profiles and the effects of chronic stress in males vs. females on GABA interneuron subtypes in the PFC. Using Sst- and Parvalbumin-fluorescence tagged reporter mice and fluorescence-activated cell sorting (FACS) combined with RNA sequencing, we identify distinct transcriptome profiles for these interneuron subtypes in the medial PFC. Based on evidence that SST interneurons are altered in depression, we then determined the effects of chronic stress on this interneuron subtype. Chronic stress causes significant dysregulation of several key pathways, including sex-specific differences in the Sst interneuron profiles. The transcriptional pathways altered by chronic stress in males overlap with enriched pathways in non-stressed females. These changes occurred predominantly in decreased expression of elongation initiation factor 2 (EIF2) signaling, suggesting that dysfunction of the translational machinery of SST interneurons could be critical to the development of depressive-like behaviors in males. In addition, SST interneurons from females exposed to chronic stress show dysregulation of different, growth factor signaling pathways.

Indexed as

AnimalsFemalegamma-Aminobutyric AcidInterneuronsMaleMiceNerve NetParvalbuminsPrefrontal CortexSex FactorsSomatostatinStress, PsychologicalTranscriptomegamma-Aminobutyric AcidParvalbuminsSomatostatin

Identifiers

PMID31712551
PMCPMC6848179
OpenAlexW2987281290

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.