Evidence map›Paper›PMID 18573641›Full record

ArticleEuropean neuropsychopharmacology : the journal of the European College of Neuropsychopharmacology2008

Antagonism of glutamatergic NMDA and mGluR5 receptors decreases consumption of food in baboon model of binge-eating disorder.

Adam Bisaga, Wojciech Danysz, Richard W Foltin

Open access · greenAbstract read
In one paragraph

Article in European neuropsychopharmacology : the journal of the European College of Neuropsychopharmacology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed, 1 pooled it
1.8field-weighted citation impact, top 15% 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

35 citing papers in PubMed, 1 synthesis or guideline pooled it, 56 citations in OpenAlex.

  1. Pooled it
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  17. Melanocortin neurons: Multiple routes to regulation of metabolism.Biochimica et biophysica acta. Molecular basis of disease · 2017
    Review
  18. Article
  19. DifferentialFrontiers in cellular neuroscience · 2017
    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

3 authors at 2 institutions in 2 countries.

Adam BisagaDivision on Substance Abuse, New York State Psychiatric Institute and Department of Psychiatry, College of Physicians and Surgeons of Columbia University, 1051 Riverside Drive, New York, NY 10032, USA. amb107@columbia.edu
Wojciech Danysz
Richard W Foltin
Columbia University · USMerLion Pharma (Germany) · DE

Funding

Translational Research on Eating DisordersR21MH065024 · NIMH · NEW YORK STATE PSYCHIATRIC INSTITUTE DBA RESEARCH FOUNDATION FOR MENTAL HYGIENE, INC · PI WALSH, B. TIMOTHY · 2002 to 2006
$2.6M
ANORECTIC DRUGS: ABUSE &BEHAVIORAL MECHANISMS OF ACTIONR01DA004130 · NIDA · NEW YORK STATE PSYCHIATRIC INSTITUTE DBA RESEARCH FOUNDATION FOR MENTAL HYGIENE, INC · PI FOLTIN, RICHARD W · 1986 to 2011
$2.2M
NIDA NIH HHS DA 04130NIDA NIH HHS R01 DA004130NIMH NIH HHS MH 65024
6 · The paper itself

Abstract

Excessive consumption of highly palatable foods may contribute to the development of weight gain. Therefore medications that selectively suppress eating of such foods would be useful in clinical practice. We compared the effects of the glutamatergic antagonists memantine and MTEP to dexfenfluramine in baboons given periodic access to highly palatable food and ad libitum access to a standard chow diet. Three days a week baboons received a sugar-coated candy during the first meal and standard standard-diet chow pellets were available in subsequent meals. All baboons derived a greater amount of energy from the single single-candy meal than from the standard diet across an entire day. Pre-treatment with dexfenfluramine, memantine, and MTEP produced decreases in candy consumption without altering candy-seeking behaviour. At the same time, dexfenfluramine and memantine, but not MTEP, produced a decrease in seeking and consumption of standard chow pellets. Both memantine and MTEP are promising agents for the treatment of obesity.

Indexed as

AnimalsAppetiteBulimia NervosaCandyConditioning, OperantConsummatory BehaviorDexfenfluramineDose-Response Relationship, DrugEatingExcitatory Amino Acid AntagonistsFemaleMaleMemantinePapio cynocephalusPyridinesReceptor, Metabotropic Glutamate 53-((2-methyl-1,3-thiazol-4-yl)ethynyl)pyridineDexfenfluramineExcitatory Amino Acid AntagonistsMemantinePyridinesReceptor, Metabotropic Glutamate 5Receptors, Metabotropic GlutamateReceptors, N-Methyl-D-AspartateSerotonin Receptor AgonistsThiazoles

Identifiers

PMID18573641
PMCPMC2591926
OpenAlexW2095549182

What OpenQuestion holds

Textmetadata
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.