Evidence map›Paper›PMID 25072322›Full record

ArticleTranslational psychiatry2014

Free D-aspartate regulates neuronal dendritic morphology, synaptic plasticity, gray matter volume and brain activity in mammals.

F Errico, R Nisticò, A Di Giorgio, M Squillace, D Vitucci, A Galbusera, S Piccinin, D Mango, L Fazio, S Middei and 8 more

Open access · goldAbstract read
In one paragraph

Article in Translational psychiatry, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed, 1 pooled it
3.7field-weighted citation impact, top 8% 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

29 citing papers in PubMed, 1 synthesis or guideline pooled it, 58 citations in OpenAlex.

  1. Pooled it
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  8. Review
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  13. d-Amino Acids and pLG72 in Alzheimer's Disease and Schizophrenia.International journal of molecular sciences · 2021
    Review
  14. Article
  15. Article
  16. Review
  17. Advances in D-Amino Acids in Neurological Research.International journal of molecular sciences · 2020
    Review
  18. Article
  19. Review
  20. 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

18 authors at 8 institutions in 1 country.

F Errico1] Laboratory of Behavioural Neuroscience, Ceinge Biotecnologie Avanzate, Naples, Italy [2] Department of Molecular Medicine and Medical Biotechnology, University of Naples 'Federico II', Naples, Italy.
R Nisticò1] Centro Europeo per la Ricerca sul Cervello (CERC)/Fondazione Santa Lucia, Rome, Italy [2] Department of Physiology and Pharmacology, Sapienza University of Rome, Rome, Italy.
A Di GiorgioIstituto di Ricovero e Cura a Carattere Scientifico 'Casa Sollievo della Sofferenza', San Giovanni Rotondo, Italy.
M SquillaceLaboratory of Behavioural Neuroscience, Ceinge Biotecnologie Avanzate, Naples, Italy.
D Vitucci1] Laboratory of Behavioural Neuroscience, Ceinge Biotecnologie Avanzate, Naples, Italy [2] Faculty of Motor Sciences, University of Naples 'Parthenope', Naples, Italy.
A GalbuseraIstituto Italiano di Tecnologia, Center for Neuroscience and Cognitive Systems, Rovereto, Italy.
S PiccininPharmacology of Synaptic Plasticity Unit, European Brain Research Institute (EBRI), Rome, Italy.
D MangoCentro Europeo per la Ricerca sul Cervello (CERC)/Fondazione Santa Lucia, Rome, Italy.
L FazioGroup of Psychiatric Neuroscience, Department of Neuroscience, Basic Sciences and Sense Organs, University of Bari 'Aldo Moro', Bari, Italy.
S MiddeiCentro Europeo per la Ricerca sul Cervello (CERC)/Fondazione Santa Lucia, Rome, Italy.
S TrizioGroup of Psychiatric Neuroscience, Department of Neuroscience, Basic Sciences and Sense Organs, University of Bari 'Aldo Moro', Bari, Italy.
N B Mercuri1] Centro Europeo per la Ricerca sul Cervello (CERC)/Fondazione Santa Lucia, Rome, Italy [2] Department of Neuroscience, Tor Vergata University Hospital Foundation, Rome, Italy.
M A TeuleCentro Europeo per la Ricerca sul Cervello (CERC)/Fondazione Santa Lucia, Rome, Italy.
D Centonze1] Centro Europeo per la Ricerca sul Cervello (CERC)/Fondazione Santa Lucia, Rome, Italy [2] Department of Neuroscience, Tor Vergata University Hospital Foundation, Rome, Italy.
A GozziIstituto Italiano di Tecnologia, Center for Neuroscience and Cognitive Systems, Rovereto, Italy.
G BlasiGroup of Psychiatric Neuroscience, Department of Neuroscience, Basic Sciences and Sense Organs, University of Bari 'Aldo Moro', Bari, Italy.
A Bertolino1] Group of Psychiatric Neuroscience, Department of Neuroscience, Basic Sciences and Sense Organs, University of Bari 'Aldo Moro', Bari, Italy [2] pRED, Neuroscience DTA, Hoffman-La Roche, Ltd, Basel, Switzerland.
A Usiello1] Laboratory of Behavioural Neuroscience, Ceinge Biotecnologie Avanzate, Naples, Italy [2] Department of Environmental, Biological and Pharmaceutical Sciences and Technologies, Second University of Naples (SUN), Caserta, Italy.
Fondazione Santa Lucia · ITUniversity of Bari Aldo Moro · ITCeinge Biotecnologie Avanzate (Italy) · ITItalian Institute of Technology · ITCasa Sollievo della Sofferenza · ITEuropean Brain Research Institute · ITParthenope University of Naples · ITUniversity of Campania "Luigi Vanvitelli" · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

D-aspartate (D-Asp) is an atypical amino acid, which is especially abundant in the developing mammalian brain, and can bind to and activate N-methyl-D-Aspartate receptors (NMDARs). In line with its pharmacological features, we find that mice chronically treated with D-Asp show enhanced NMDAR-mediated miniature excitatory postsynaptic currents and basal cerebral blood volume in fronto-hippocampal areas. In addition, we show that both chronic administration of D-Asp and deletion of the gene coding for the catabolic enzyme D-aspartate oxidase (DDO) trigger plastic modifications of neuronal cytoarchitecture in the prefrontal cortex and CA1 subfield of the hippocampus and promote a cytochalasin D-sensitive form of synaptic plasticity in adult mouse brains. To translate these findings in humans and consistent with the experiments using Ddo gene targeting in animals, we performed a hierarchical stepwise translational genetic approach. Specifically, we investigated the association of variation in the gene coding for DDO with complex human prefrontal phenotypes. We demonstrate that genetic variation predicting reduced expression of DDO in postmortem human prefrontal cortex is mapped on greater prefrontal gray matter and activity during working memory as measured with MRI. In conclusion our results identify novel NMDAR-dependent effects of D-Asp on plasticity and physiology in rodents, which also map to prefrontal phenotypes in humans.

Indexed as

AdultAnimalsBrainD-Aspartate OxidaseD-Aspartic AcidFemaleGene DeletionGene Expression Regulation, EnzymologicGray MatterHippocampusHumansMagnetic Resonance ImagingMaleMemory, Short-TermMiceMice, Inbred C57BLD-Aspartate OxidaseD-Aspartic AcidReceptors, N-Methyl-D-AspartateRNA, Messenger

Identifiers

PMID25072322
PMCPMC4119226
OpenAlexW2080380788

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.