Evidence map›Paper›PMID 24322205›Full record

ArticleMolecular psychiatry2014

Modulation of behavioral networks by selective interneuronal inactivation.

M J Schmidt, S Horvath, P Ebert, J L Norris, E H Seeley, J Brown, L Gellert, M Everheart, K A Garbett, T W Grice and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in Molecular psychiatry, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
6.0field-weighted citation impact, top 4% 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

26 citing papers in PubMed, 35 citations in OpenAlex.

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  11. Cannabinoid CBFrontiers in physiology · 2019
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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

12 authors at 2 institutions in 3 countries.

M J Schmidt1] Neuroscience Graduate Program, Vanderbilt University, Nashville, TN, USA [2] Department of Psychiatry, Vanderbilt University, Nashville, TN, USA.
S Horvath1] Department of Psychiatry, Vanderbilt University, Nashville, TN, USA [2] Department of Psychiatry, University of Szeged, Szeged, Hungary.
P EbertDepartment of Psychiatry, Vanderbilt University, Nashville, TN, USA.
J L NorrisDepartment of Biochemistry, Vanderbilt University, Nashville, TN, USA.
E H SeeleyDepartment of Biochemistry, Vanderbilt University, Nashville, TN, USA.
J BrownDepartment of Psychiatry, Vanderbilt University, Nashville, TN, USA.
L GellertDepartment of Psychiatry, University of Szeged, Szeged, Hungary.
M EverheartDepartment of Psychiatry, Vanderbilt University, Nashville, TN, USA.
K A GarbettDepartment of Psychiatry, Vanderbilt University, Nashville, TN, USA.
T W GriceDepartment of Psychiatry, Vanderbilt University, Nashville, TN, USA.
R M CaprioliDepartment of Biochemistry, Vanderbilt University, Nashville, TN, USA.
K Mirnics1] Department of Psychiatry, Vanderbilt University, Nashville, TN, USA [2] Department of Psychiatry, University of Szeged, Szeged, Hungary [3] Vanderbilt Kennedy Center for Research on Human Development, Vanderbilt University, Nashville, TN, USA.
Vanderbilt University · USUniversity of Szeged · HU

Funding

Training (pp 214-245)P41GM103391 · NIGMS · VANDERBILT UNIVERSITY · PI CAPRIOLI, RICHARD M · 2012 to 2020
$17.7M
Program in NeurogenomicsT32MH065215 · NIMH · VANDERBILT UNIVERSITY · PI ROGER J COLBRAN · 2002 to 2026
$6.4M
Neocortical Transcriptome Changes in SchizophreniaR01MH067234 · NIMH · VANDERBILT UNIVERSITY · PI MIRNICS, KAROLY · 2003 to 2021
$4.7M
IMAGING MASS SPECTROMETRY RESEARCH RESOURCE AT VANDERBILT UNIVERSITYP41RR031461 · NCRR · VANDERBILT UNIVERSITY · PI CAPRIOLI, RICHARD M · 2011 to 2011
$2.2M
NCRR NIH HHS P41 RR031461NIGMS NIH HHS P41 GM103391NIMH NIH HHS R01 MH067234NIMH NIH HHS T32 MH065215
6 · The paper itself

Abstract

Gamma-aminobutyric acid (GABA)-ergic disturbances are hallmark features of schizophrenia and other neuropsychiatric disorders and encompass multiple interneuronal cell types. Using bacterial artificial chromosome-driven, miRNA silencing technology we generated transgenic mouse lines that suppress glutamic acid decarboxylase 1 (GAD1) in either cholecystokinin (CCK)- or neuropeptide Y (NPY)-expressing interneurons. In situ lipidomic and proteomic analyses on brain tissue sections revealed distinct, brain region-specific profiles in each transgenic line. Behavioral analyses revealed that suppression of GAD1 in CCK+ interneurons resulted in locomotor and olfactory sensory changes, whereas suppression in NPY+ interneurons affected anxiety-related behaviors and social interaction. Both transgenic mouse lines had altered sensitivity to amphetamine albeit in opposite directions. Together, these data argue that reduced GAD1 expression leads to altered molecular and behavioral profiles in a cell type-dependent manner, and that these subpopulations of interneurons are strong and opposing modulators of dopamine system function. Furthermore, our findings also support the hypothesis that neuronal networks are differentially controlled by diverse inhibitory subnetworks.

Indexed as

AmphetamineAnimalsAnxietyBehaviorBrainCentral Nervous System StimulantsCholecystokiningamma-Aminobutyric AcidGlutamate DecarboxylaseInterneuronsMaleMice, Inbred C57BLMice, TransgenicMotor ActivityNeuropeptide YOlfactory PerceptionAmphetamineCentral Nervous System StimulantsCholecystokiningamma-Aminobutyric AcidGlutamate Decarboxylaseglutamate decarboxylase 1Neuropeptide Y

Identifiers

PMID24322205
PMCPMC4179403
OpenAlexW2082049393

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.