Evidence map›Paper›PMID 24121738›Full record

ArticleNature neuroscience2013

Age-dependent regulation of synaptic connections by dopamine D2 receptors.

Jie-Min Jia, Jun Zhao, Zhonghua Hu, Daniel Lindberg, Zheng Li

Open access · greenAbstract read
In one paragraph

Article in Nature neuroscience, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed
3.0field-weighted citation impact, top 9% 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

46 citing papers in PubMed, 72 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors at 1 institution in 1 country.

Jie-Min JiaUnit on Synapse Development and Plasticity, National Institute of Mental Health, US National Institutes of Health, Bethesda, Maryland, USA.
Jun Zhao
Zhonghua Hu
Daniel Lindberg
National Institutes of Health · US

Funding

Non-apoptotic function of casapses in synapsesZIAMH002881 · NIMH · NATIONAL INSTITUTE OF MENTAL HEALTH · PI LI, ZHENG · 2009 to 2025
$18.9M
NEURAL TISSUE MICROCHIP INTERFACEZ01MH002281 · NIMH · NATIONAL INSTITUTE OF MENTAL HEALTH · PI OLIVER, A P · 1985 to 1989
–
Intramural NIH HHS ZIA MH002881NIMH NIH HHS ZIA MH002281
6 · The paper itself

Abstract

Dopamine D2 receptors (D2R) are G protein-coupled receptors that modulate synaptic transmission and are important for various brain functions, including learning and working memory. Abnormal D2R signaling has been implicated in psychiatric disorders such as schizophrenia. Here we report a new function of D2R in dendritic spine morphogenesis. Activation of D2R reduced spine number via GluN2B- and cAMP-dependent mechanisms in mice. Notably, this regulation occurred only during adolescence. During this period, D2R overactivation caused by mutations in the schizophrenia risk gene Dtnbp1 led to spine deficiency, dysconnectivity in the entorhinal-hippocampal circuit and impairment of spatial working memory. Notably, these defects could be ameliorated by D2R blockers administered during adolescence. Our findings suggest an age-dependent function of D2R in spine development, provide evidence that D2R dysfunction during adolescence impairs neuronal circuits and working memory, and indicate that adolescent interventions to prevent aberrant D2R activity protect against cognitive impairment.

Indexed as

Aging6-Cyano-7-nitroquinoxaline-2,3-dioneAge FactorsAnesthetics, LocalAnimalsCells, CulturedCerebral CortexDark AdaptationDopamine AgentsExcitatory Amino Acid AntagonistsExcitatory Postsynaptic PotentialsGene Expression RegulationHippocampusIn Vitro TechniquesMaze LearningMice6-Cyano-7-nitroquinoxaline-2,3-dioneAnesthetics, LocalDopamine AgentsExcitatory Amino Acid AntagonistsNR2B NMDA receptorReceptors, Dopamine D2Receptors, N-Methyl-D-Aspartate

Identifiers

PMID24121738
PMCPMC3832846
OpenAlexW2071150768

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.