Evidence map›Paper›PMID 28809400›Full record

ArticleMolecular psychiatry2018

Prenatal one-carbon metabolism dysregulation programs schizophrenia-like deficits.

A Alachkar, L Wang, R Yoshimura, A R Hamzeh, Z Wang, N Sanathara, S M Lee, X Xu, G W Abbott, O Civelli

Abstract read
In one paragraph

Article in Molecular psychiatry, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.0field-weighted citation impact, top 24% 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

21 citing papers in PubMed, 31 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Humanized dopamine DJournal of neuroscience research · 2024
    Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  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

10 authors at 2 institutions in 2 countries.

A AlachkarDepartment of Pharmacology, School of Medicine, University of California, Irvine, Irvine, CA, USA.
L WangDepartment of Pharmacology, School of Medicine, University of California, Irvine, Irvine, CA, USA.
R YoshimuraDepartment of Pharmacology, School of Medicine, University of California, Irvine, Irvine, CA, USA.
A R HamzehCentre for Arab Genomic Studies, Dubai, United Arab Emirates.
Z WangDepartment of Pharmacology, School of Medicine, University of California, Irvine, Irvine, CA, USA.
N SanatharaDepartment of Pharmacology, School of Medicine, University of California, Irvine, Irvine, CA, USA.
S M LeeDepartment of Pharmacology, School of Medicine, University of California, Irvine, Irvine, CA, USA.
X XuDepartment of Anatomy & Neurobiology, School of Medicine, University of California, Irvine, Irvine, CA, USA.
G W AbbottDepartment of Pharmacology, School of Medicine, University of California, Irvine, Irvine, CA, USA.
O CivelliDepartment of Pharmacology, School of Medicine, University of California, Irvine, Irvine, CA, USA.
University of California, Irvine · USCentre for Arab Genomic Studies · AE

Funding

Inhibitory neuron circuit organization and function in prefrontal cortex.R01MH105427 · NIMH · UNIVERSITY OF CALIFORNIA-IRVINE · PI GOLSHANI, PEYMAN, XU, XIANGMIN · 2015 to 2019
$2.3M
Neural circuit organization and function of the bed nucleus of the stria terminalisR01MH113026 · NIMH · UNIVERSITY OF CALIFORNIA-IRVINE · PI XU, XIANGMIN · 2017 to 2021
$2.2M
A novel neuropeptide system involved in drug abuseR01DA024746 · NIDA · UNIVERSITY OF CALIFORNIA-IRVINE · PI CIVELLI, OLIVIER · 2010 to 2013
$1.5M
NIDA NIH HHS R01 DA024746NIMH NIH HHS R01 MH105427NIMH NIH HHS R01 MH113026
6 · The paper itself

Abstract

The methionine-folate cycle-dependent one-carbon metabolism is implicated in the pathophysiology of schizophrenia. Since schizophrenia is a developmental disorder, we examined the effects that perturbation of the one-carbon metabolism during gestation has on mice progeny. Pregnant mice were administered methionine equivalent to double their daily intake during the last week of gestation. Their progeny (MET mice) exhibited schizophrenia-like social deficits, cognitive impairments and elevated stereotypy, decreased neurogenesis and synaptic plasticity, and abnormally reduced local excitatory synaptic connections in CA1 neurons. Neural transcript expression of only one gene, encoding the Npas4 transcription factor, was >twofold altered (downregulated) in MET mice; strikingly, similar Npas4 downregulation occurred in the prefrontal cortex of human patients with schizophrenia. Finally, therapeutic actions of typical (haloperidol) and atypical (clozapine) antipsychotics in MET mice mimicked effects in human schizophrenia patients. Our data support the validity of MET mice as a model for schizophrenia, and uncover methionine metabolism as a potential preventive and/or therapeutic target.

Indexed as

AnimalsAntipsychotic AgentsBasic Helix-Loop-Helix ProteinsCA1 Region, HippocampalClozapineDevelopmental DisabilitiesDisease Models, AnimalFemaleFolic AcidHaloperidolHumansMaleMethionineMiceNeurogenesisNeuronal PlasticityAntipsychotic AgentsBasic Helix-Loop-Helix ProteinsClozapineFolic AcidHaloperidolMethionineNpas4 protein, mouseOne-Carbon Group TransferasesTetrahydrofolates

Identifiers

PMID28809400
PMCPMC6432924
OpenAlexW2750215515

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.