Evidence map›Paper›PMID 33907230›Full record

ArticleScientific reports2021

Altered neural oscillations and behavior in a genetic mouse model of NMDA receptor hypofunction.

David D Aguilar, Leana K Radzik, Felipe L Schiffino, Oluwarotimi O Folorunso, Mark R Zielinski, Joseph T Coyle, Darrick T Balu, James M McNally

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

19 citing papers in PubMed, 25 citations in OpenAlex.

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  13. SELENBP1 overexpression in the prefrontal cortex underlies negative symptoms of schizophrenia.Proceedings of the National Academy of Sciences of the United States of America · 2022
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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

8 authors at 4 institutions in 1 country.

David D AguilarVA Boston Healthcare System, West Roxbury, MA, USA. David_Aguilar@hms.harvard.edu.
Leana K RadzikDepartment of Neuroscience, Stonehill College, Easton, MA, USA.
Felipe L SchiffinoVA Boston Healthcare System, West Roxbury, MA, USA.
Oluwarotimi O FolorunsoDepartment of Psychiatry, Harvard Medical School, Boston, MA, USA.
Mark R ZielinskiVA Boston Healthcare System, West Roxbury, MA, USA.
Joseph T CoyleDepartment of Psychiatry, Harvard Medical School, Boston, MA, USA.
Darrick T BaluDepartment of Psychiatry, Harvard Medical School, Boston, MA, USA.
James M McNallyVA Boston Healthcare System, West Roxbury, MA, USA.
Harvard University · USMcLean Hospital · USVA Boston Healthcare System · USStonehill College · US

Funding

Stuart T. Hauser Research Training Program in Biological and Social Psychiatry.T32MH016259 · NIMH · JUDGE BAKER CHILDREN'S CENTER · PI Marek Kubicki, Martha E. Shenton · 1985 to 2026
$8.4M
Stabilizing the Tripartite Synaptic Complex Following TBIR01NS098740 · NINDS · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI Joacir Graciolli Graciolli Cordeiro, Daniel Jon Liebl · 2017 to 2026
$4.7M
Defining the Role of Glial D-serine in Alzheimer's DiseaseR03AG063201 · NIA · MCLEAN HOSPITAL · PI BALU, DARRICK T · 2019 to 2020
$328k
Basal forebrain parvalbumin neurons regulate attention by controlling cortical oscillationsF32MH119838 · NIMH · HARVARD MEDICAL SCHOOL · PI SCHIFFINO, FELIPE LOPES · 2020 to 2020
$72k
Sleep Loss and Inflammation in the Neurovascular UnitIK2BX002823 · VA · VA BOSTON HEALTH CARE SYSTEM · PI ZIELINSKI, MARK ROBERT · 2016 to 2020
–
Tuning cortical E/I balance for translational modeling of psychiatric disordersI01BX004500 · VA · VA BOSTON HEALTH CARE SYSTEM · PI JAMES M MCNALLY · 2019 to 2026
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Improving cortical function & cognition in schizophrenia by modulation of mGluR5IK2BX002130 · VA · VA BOSTON HEALTH CARE SYSTEM · PI MCNALLY, JAMES M · 2014 to 2018
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BLRD VA I01 BX004500BLRD VA IK2 BX002130BLRD VA IK2 BX002823NIA NIH HHS 1R03AG063201-01NIA NIH HHS R03 AG063201NIMH NIH HHS F32 MH119838NIMH NIH HHS F32MH119838NIMH NIH HHS T32 MH016259NIMH NIH HHS T32MH016259NINDS NIH HHS R01 NS098740NINDS NIH HHS R01NS098740-02United States-Israel Binational Science Foundation 2019021
6 · The paper itself

Abstract

Abnormalities in electroencephalographic (EEG) biomarkers occur in patients with schizophrenia and those clinically at high risk for transition to psychosis and are associated with cognitive impairment. Converging evidence suggests N-methyl-D-aspartate receptor (NMDAR) hypofunction plays a central role in the pathophysiology of schizophrenia and likely contributes to biomarker impairments. Thus, characterizing these biomarkers is of significant interest for early diagnosis of schizophrenia and development of novel treatments. We utilized in vivo EEG recordings and behavioral analyses to perform a battery of electrophysiological biomarkers in an established model of chronic NMDAR hypofunction, serine racemase knockout (SRKO) mice, and their wild-type littermates. SRKO mice displayed impairments in investigation-elicited gamma power that corresponded with reduced short-term social recognition and enhanced background (pre-investigation) gamma activity. Additionally, SRKO mice exhibited sensory gating impairments in both evoked-gamma power and event-related potential amplitude. However, other biomarkers including the auditory steady-state response, sleep spindles, and state-specific power spectral density were generally neurotypical. In conclusion, SRKO mice demonstrate how chronic NMDAR hypofunction contributes to deficits in certain translationally-relevant EEG biomarkers altered in schizophrenia. Importantly, our gamma band findings suggest an aberrant signal-to-noise ratio impairing cognition that occurs with NMDAR hypofunction, potentially tied to impaired task-dependent alteration in functional connectivity.

Indexed as

AnimalsBiomarkersDisease Models, AnimalElectroencephalographyFemaleGamma RhythmMaleMiceMice, Inbred C57BLMice, KnockoutRacemases and EpimerasesReceptors, N-Methyl-D-AspartateSchizophreniaSensory GatingSerine RacemaseSocial BehaviorBiomarkersRacemases and EpimerasesReceptors, N-Methyl-D-AspartateSerine Racemase

Identifiers

PMID33907230
PMCPMC8079688
OpenAlexW3158585464

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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.