Evidence map›Paper›PMID 26919286›Full record

ArticleBehavioural pharmacology2016

Brain catechol-O-methyltransferase (COMT) inhibition by tolcapone counteracts recognition memory deficits in normal and chronic phencyclidine-treated rats and in COMT-Val transgenic mice.

Eric R Detrait, Greg V Carr, Daniel R Weinberger, Yves Lamberty

Abstract read
In one paragraph

Article in Behavioural pharmacology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.2field-weighted citation impact, top 22% 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

13 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Review
  6. Interaction of silver nanoparticles with catecholBiochemistry and biophysics reports · 2021
    Article
  7. Entacapone promotes hippocampal neurogenesis in mice.Neural regeneration research · 2021
    Article
  8. Effort-related decision making in humanized COMT mice: Effects of ValPharmacology, biochemistry, and behavior · 2020
    Article
  9. Review
  10. Inhibition of Catechol-Frontiers in behavioral neuroscience · 2020
    Article
  11. Article
  12. Potential Impact ofJournal of cardiovascular development and disease · 2018
    Article
  13. 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

4 authors at 3 institutions in 2 countries.

Eric R DetraitaUCB Biopharma s.p.r.l., Neuroscience Therapeutic Area, Chemin du Foriest, B-1420 Braine-l'Alleud, Belgium bLieber Institute for Brain Development Departments of cPsychiatry dNeurology eNeuroscience, Institute of Genetic Medicine, Johns Hopkins School of Medicine, Baltimore fClinical Brain Disorders Branch, National Institute of Mental Health, NIH, Bethesda, Maryland, USA.
Greg V Carr
Daniel R Weinberger
Yves Lamberty
UCB Pharma (Belgium) · BEJohns Hopkins University · USLieber Institute for Brain Development · US

Funding

Transgenic Mouse Model for Mental Disorders including schizophreniaZ01MH002906 · NIMH · NATIONAL INSTITUTE OF MENTAL HEALTH · PI CHEN, JINGSHAN · 2007 to 2008
$2.2M
Transgenic Mouse Model for Mental Disorders including schizophreniaZICMH002906 · NIMH · NATIONAL INSTITUTE OF MENTAL HEALTH · PI WEINBERGER, DANIEL · 2009 to 2011
$1.6M
Intramural NIH HHS Z01 MH002906Intramural NIH HHS ZIC MH002906
6 · The paper itself

Abstract

The critical involvement of dopamine in cognitive processes has been well established, suggesting that therapies targeting dopamine metabolism may alleviate cognitive dysfunction. Catechol-O-methyl transferase (COMT) is a catecholamine-degrading enzyme, the substrates of which include dopamine, epinephrine, and norepinephrine. The present work illustrates the potential therapeutic efficacy of COMT inhibition in alleviating cognitive impairment. A brain-penetrant COMT inhibitor, tolcapone, was tested in normal and phencyclidine-treated rats and COMT-Val transgenic mice. In a novel object recognition procedure, tolcapone counteracted a 24-h-dependent forgetting of a familiar object as well as phencyclidine-induced recognition deficits in the rats at doses ranging from 7.5 to 30 mg/kg. In contrast, entacapone, a COMT inhibitor that does not readily cross the blood-brain barrier, failed to show efficacy at doses up to 30 mg/kg. Tolcapone at a dose of 30 mg/kg also improved novel object recognition performance in transgenic mice, which showed clear recognition deficits. Complementing earlier studies, our results indicate that central inhibition of COMT positively impacts recognition memory processes and might constitute an appealing treatment for cognitive dysfunction related to neuropsychiatric disorders.

Indexed as

AnimalsBenzophenonesBlood-Brain BarrierBrainCatechol O-MethyltransferaseCatechol O-Methyltransferase InhibitorsCatecholsCognition DisordersDopamineDose-Response Relationship, DrugMaleMemory DisordersMiceMice, TransgenicNitrilesNitrophenolsBenzophenonesCatechol O-MethyltransferaseCatechol O-Methyltransferase InhibitorsCatecholsDopamineentacaponeNitrilesNitrophenolsPhencyclidineTolcapone

Identifiers

PMID26919286
PMCPMC4935608
OpenAlexW2315720973

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.