Evidence map›Paper›PMID 32778145›Full record

ArticleMolecular brain2020

Altered dopaminergic pathways and therapeutic effects of intranasal dopamine in two distinct mouse models of autism.

Owen Y Chao, Salil S Pathak, Hao Zhang, Nathan Dunaway, Jay-Shake Li, Claudia Mattern, Susanne Nikolaus, Joseph P Huston, Yi-Mei Yang

Open access · goldAbstract read
In one paragraph

Article in Molecular brain, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed, 3 pooled it
4.8field-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

40 citing papers in PubMed, 3 syntheses or guidelines pooled it, 61 citations in OpenAlex.

  1. Pooled it
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  8. How does oxytocin modulate human behavior?Molecular psychiatry · 2025
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  16. Transcriptional Dysregulation and Impaired Neuronal Activity inInternational journal of molecular sciences · 2023
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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 5 institutions in 3 countries.

Owen Y ChaoDepartment of Biomedical Sciences, University of Minnesota Medical School, 1035 University Drive, Duluth, MN, 55812, USA.
Salil S PathakDepartment of Biomedical Sciences, University of Minnesota Medical School, 1035 University Drive, Duluth, MN, 55812, USA.
Hao ZhangDepartment of Biomedical Sciences, University of Minnesota Medical School, 1035 University Drive, Duluth, MN, 55812, USA.
Nathan DunawayDepartment of Biomedical Sciences, University of Minnesota Medical School, 1035 University Drive, Duluth, MN, 55812, USA.
Jay-Shake LiDepartment of Psychology, National Chung Cheng University, Minhsiung, Chiayi, Taiwan, Republic of China.
Claudia MatternM et P Pharma AG, Emmetten, Switzerland.
Susanne NikolausClinic of Nuclear Medicine, Heinrich Heine University of Düsseldorf, Düsseldorf, Germany.
Joseph P HustonCenter for Behavioral Neuroscience, Heinrich Heine University of Düsseldorf, Universitaetsstr. 1, 40225, Düsseldorf, Germany. jph@uni-duesseldorf.de.
Yi-Mei YangDepartment of Biomedical Sciences, University of Minnesota Medical School, 1035 University Drive, Duluth, MN, 55812, USA. ymyang@d.umn.edu.ORCID 0000-0003-1491-8106
University of Minnesota, Duluth · USHeinrich Heine University Düsseldorf · DENational Chung Cheng University · TWNova Southeastern University · USUniversity of Minnesota · US

Funding

Aberrant neuronal excitability of the cerebellum in mouse models of autism spectrum disorderR15NS112964 · NINDS · UNIVERSITY OF MINNESOTA DULUTH · PI YANG, YI-MEI (AMY) · 2019 to 2019
$448k
NINDS NIH HHS R15 NS112964
6 · The paper itself

Abstract

The dopamine (DA) system has a profound impact on reward-motivated behavior and is critically involved in neurodevelopmental disorders, such as autism spectrum disorder (ASD). Although DA defects are found in autistic patients, it is not well defined how the DA pathways are altered in ASD and whether DA can be utilized as a potential therapeutic agent for ASD. To this end, we employed a phenotypic and a genetic ASD model, i.e., Black and Tan BRachyury T

Indexed as

Administration, IntranasalAnimalsAttentionAutistic DisorderBehavior, AnimalBrachyury ProteinCorpus StriatumDisease Models, AnimalDopamineDopamine Plasma Membrane Transport ProteinsExploratory BehaviorFetal ProteinsFractalsFragile X Messenger Ribonucleoprotein 1Mice, Inbred C57BLMice, KnockoutBrachyury ProteinDopamineDopamine Plasma Membrane Transport ProteinsFetal ProteinsFmr1 protein, mouseFragile X Messenger Ribonucleoprotein 1T-Box Domain ProteinsTyrosine 3-MonooxygenaseAutismBTBRFmr1Fragile X syndromeSocial behaviorStriatum

Identifiers

PMID32778145
PMCPMC7418402
OpenAlexW3048864623

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.