Evidence map›Paper›PMID 31392357›Full record

ArticlePsychopharmacology2019

A translational EEG-based approach to assess modulation of long-lasting NMDAR-dependent synaptic plasticity.

Jeffrey S Burgdorf, E P Christian, L Sørensen, P K Stanton, K Leaderbrand, T M Madsen, M A Khan, R A Kroes, J R Moskal

Registry-linked trialOpen access · hybridAbstract read
In one paragraph

Article in Psychopharmacology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06957808 (Investigating the Effect of Diroximel Fumarate on Glutathione in Schizophrenia), which is not on this map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
0.9field-weighted citation impact, top 31% 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.

NCT06957808 narecruitingnot on this mapstarted 2025, after this paper: background citation

Investigating the Effect of Diroximel Fumarate on Glutathione in Schizophrenia

TypeinterventionalSponsorKing's College LondonRan2025 to 2027Enrolled30ConditionsSchizophrenia DisordersArmsDiroximel fumarate (DRF), Placebo
3 · Its place in the literature

Who cites it

16 citing papers in PubMed, 21 citations in OpenAlex.

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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

9 authors at 3 institutions in 1 country.

Jeffrey S BurgdorfAptinyx Inc., 1801 Maple Ave, Suite 4300, Evanston, IL, 60201, USA. jeffreyburgdorf@aptinyx.com.ORCID http://orcid.org/0000-0001-6662-6717
E P ChristianAptinyx Inc., 1801 Maple Ave, Suite 4300, Evanston, IL, 60201, USA.
L SørensenAptinyx Inc., 1801 Maple Ave, Suite 4300, Evanston, IL, 60201, USA.
P K StantonCell Biology & Anatomy, New York Medical College, Valhalla, NY, USA.
K LeaderbrandAptinyx Inc., 1801 Maple Ave, Suite 4300, Evanston, IL, 60201, USA.
T M MadsenAptinyx Inc., 1801 Maple Ave, Suite 4300, Evanston, IL, 60201, USA.
M A KhanAptinyx Inc., 1801 Maple Ave, Suite 4300, Evanston, IL, 60201, USA.
R A KroesAptinyx Inc., 1801 Maple Ave, Suite 4300, Evanston, IL, 60201, USA.
J R MoskalAptinyx Inc., 1801 Maple Ave, Suite 4300, Evanston, IL, 60201, USA.
Aptinyx (United States) · USNorthwestern University · USNew York Medical College · US

Funding

IGFI and DepressionR01MH094835 · NIMH · NORTHWESTERN UNIVERSITY · PI BURGDORF, JEFFREY SCOTT · 2012 to 2016
$1.9M
NIH HHS CA199928NIMH NIH HHS MH094835
6 · The paper itself

Abstract

backgroundNYX-2925 is a novel N-methyl-D-aspartate receptor (NMDAR) modulator that has been shown to facilitate both NMDAR-dependent long-term potentiation (LTP) in vitro and learning and memory in vivo.

objectiveThe present studies examine the effects of NYX-2925 on NMDAR-dependent auditory LTP (aLTP) in vivo.

methodsNMDAR-dependent aLTP and NMDAR-dependent auditory mismatch negativity (MMN) was measured, as well as changes in resting-state qEEG power.

resultsNYX-2925 (1, 10 mg/kg PO) increased aLTP 1 h after auditory tetanus measured by the post- minus pre-tetanus difference waveform 140-180 ms post tone onset. NYX-2925 (0.1, 1 mg/kg PO) facilitated MMN measured by the difference waveform (i.e., deviant minus standard tones). NYX-2925 (0.1, 1, 10 mg/kg PO) also enhanced resting-state alpha qEEG power. Conversely, the NMDAR glutamate site antagonist CPP (10 mg/kg IP) reduces alpha power and MMN and produces an opposite effect as NYX-2925 on aLTP.

conclusionsTogether, these data suggest that the activation of the NMDAR by NYX-2925 enhances synaptic plasticity in vivo, which may both reduce symptoms of neurological disorders and serve as a biomarker for drug effects. This is the first demonstration of a long-lasting (1-h post-tetanus) effect of NMDAR modulation on synaptic plasticity processes in vivo using a noninvasive technique in freely behaving animals.

Indexed as

AnimalsElectroencephalographyExcitatory Amino Acid AntagonistsLearningLong-Term PotentiationMaleMemoryNeuronal PlasticityRatsRats, Sprague-DawleyReceptors, N-Methyl-D-AspartateSpiro CompoundsTranslational Research, BiomedicalExcitatory Amino Acid AntagonistsNYX-2925Receptors, N-Methyl-D-AspartateSpiro CompoundsAuditory-evoked potentialsEEGLTPMismatch negativityNMDA receptors

Identifiers

PMID31392357
PMCPMC6892763
OpenAlexW2964394344

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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.