Evidence map›Paper›PMID 34702791›Full record

ArticleBiomolecules & therapeutics2022

Autism-Like Behavioral Phenotypes in Mice Treated with Systemic N-Methyl-D-Aspartate.

Keremkleroo Jym Adil, Edson Luck Gonzales, Chilly Gay Remonde, Kyung-Jun Boo, Se Jin Jeon, Chan Young Shin

Open access · hybridAbstract read
In one paragraph

Article in Biomolecules & therapeutics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.2field-weighted citation impact, top 49% 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

3 citing papers in PubMed, 5 citations in OpenAlex.

  1. Review
  2. Article
  3. 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.

Keremkleroo Jym AdilSchool of Medicine and Center for Neuroscience Research, Konkuk University, Seoul 05029, Republic of Korea.
Edson Luck GonzalesSchool of Medicine and Center for Neuroscience Research, Konkuk University, Seoul 05029, Republic of Korea.
Chilly Gay RemondeSchool of Medicine and Center for Neuroscience Research, Konkuk University, Seoul 05029, Republic of Korea.
Kyung-Jun BooSchool of Medicine and Center for Neuroscience Research, Konkuk University, Seoul 05029, Republic of Korea.
Se Jin JeonSchool of Medicine and Center for Neuroscience Research, Konkuk University, Seoul 05029, Republic of Korea.
Chan Young ShinSchool of Medicine and Center for Neuroscience Research, Konkuk University, Seoul 05029, Republic of Korea.
Konkuk University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Autism spectrum disorder (ASD) having core characteristics of social interaction problems and repetitive behaviors and interests affects individuals at varying degrees and comorbidities, making it difficult to determine the precise etiology underlying the symptoms. Given its heterogeneity, ASD is difficult to treat and the development of therapeutics is slow due to the scarcity of animal models that are easy to produce and screen with. Based on the theory of excitation/inhibition imbalance in the brain with ASD which involves glutamatergic and/or GABAergic neurotransmission, a pharmacologic agent to modulate these receptors might be a good starting point for modeling. N-methyl-D-aspartic acid (NMDA) is an amino acid derivative acting as a specific agonist at the NMDA receptor and therefore imitates the action of the neurotransmitter glutamate on that receptor. In contrast to glutamate, NMDA selectively binds to and regulates the NMDA receptor, but not other glutamate receptors such as AMPA and kainite receptors. Given this role, we aimed to determine whether NMDA administration could result in autistic-like behavior in adolescent mice. Both male and female mice were treated with saline or NMDA (50 and 75 mg/kg) and were tested on various behavior experiments. Interestingly, acute NMDA-treated mice showed social deficits and repetitive behavior similar to ASD phenotypes. These results support the excitation/inhibition imbalance theory of ASD and that NMDA injection can be used as a pharmacologic model of ASD-like behaviors.

Indexed as

ASD animal modelAutism spectrum disorderE/I imbalanceNMDARepetitive behaviorSocial deficit

Identifiers

PMID34702791
PMCPMC9047488
OpenAlexW3209611254

What OpenQuestion holds

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LicenceCC BY-NC
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.