Evidence map›Paper›PMID 22245542›Full record

ArticleEuropean neuropsychopharmacology : the journal of the European College of Neuropsychopharmacology2012

Chronic treatment with lithium or valproate modulates the expression of Homer1b/c and its related genes Shank and Inositol 1,4,5-trisphosphate receptor.

Andrea de Bartolomeis, Carmine Tomasetti, Maria Cicale, Pei-Xiong Yuan, Husseini K Manji

Open access · greenAbstract read
In one paragraph

Article in European neuropsychopharmacology : the journal of the European College of Neuropsychopharmacology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 1 pooled it
2.9field-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

16 citing papers in PubMed, 1 synthesis or guideline pooled it, 40 citations in OpenAlex.

  1. Pooled it
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  14. Lithium and GSK3-β promoter gene variants influence white matter microstructure in bipolar disorder.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2013
    Article
  15. Article
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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

5 authors at 3 institutions in 2 countries.

Andrea de BartolomeisLaboratory of Molecular Psychiatry and Psychopharmacotherapeutics, Department of Neuroscience, Section of Psychiatry, University School of Medicine "Federico II", Naples, Italy. adebarto@unina.it
Carmine Tomasetti
Maria Cicale
Pei-Xiong Yuan
Husseini K Manji
Federico II University Hospital · ITNational Institute of Mental Health · USNational Institutes of Health · US

Funding

Testing whether the enzyme GSK-3 is a therapeutically relevant target of lithiumZ01MH002841 · NIMH · NATIONAL INSTITUTE OF MENTAL HEALTH · PI MANJI, HUSSEINI K · 2004 to 2008
$1.1M
Intramural NIH HHS Z01 MH002841
6 · The paper itself

Abstract

Homer proteins are associated with both dopaminergic and glutamatergic function. In addition, these proteins are implicated in many signal transduction pathways that are also putative targets of the mood stabilizers lithium and valproate (VPA). This study investigated the effect of in vivo chronic administration of therapeutically-relevant doses of lithium and VPA on the expression of the inducible (Homer1a and ania-3) and constitutive (Homer1b/c) isoforms of the Homer1 gene in rat brain, and of two other Homer-related genes: Inositol 1,4,5 trisphosphate receptor (IP3R) and Shank. Homer1b/c was significantly decreased in cortex by VPA, and in striatal and accumbal subregions by both lithium and VPA. Both mood stabilizers reduced Homer1b/c expression in the dorsolateral caudate-putamen, while only VPA decreased gene expression in all other striatal subregions. Shank and IP3R were downregulated by both mood stabilizers in the cortex. Neither chronic lithium nor VPA affected Homer immediate-early genes. These results suggest that lithium and VPA similarly modulate the expression of structural postsynaptic genes with topographic specificity in cortical and subcortical regions. Thus, Homer may represent an additional molecular substrate for mood stabilizers, and a potential link with dopaminergic function.

Indexed as

Analysis of VarianceAnimalsAntimanic AgentsAutoradiographyBrainCarrier ProteinsGene Expression RegulationHomer Scaffolding ProteinsInositol 1,4,5-Trisphosphate ReceptorsLithium CarbonateMaleNerve Tissue ProteinsProtein BindingProtein IsoformsRatsRats, Inbred WKYAntimanic AgentsCarrier ProteinsHomer1 protein, ratHomer Scaffolding ProteinsInositol 1,4,5-Trisphosphate ReceptorsLithium CarbonateNerve Tissue ProteinsProtein IsoformsValproic Acid

Identifiers

PMID22245542
PMCPMC3361644
OpenAlexW1987780985

What OpenQuestion holds

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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.