Evidence map›Paper›PMID 15619109›Full record

ArticlePsychopharmacology2005

Selective serotonin 5-HT2A receptor antagonist EMD 281014 improves delayed matching performance in young and aged rhesus monkeys.

Alvin V Terry, Jerry J Buccafusco, Gerd D Bartoszyk

Abstract read
PubMed Publisher
In one paragraph

Article in Psychopharmacology, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.1field-weighted citation impact, top 28% 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

18 citing papers in PubMed, 49 citations in OpenAlex.

  1. Review
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  6. The serotonergic system and cognitive function.Translational neuroscience · 2016
    Review
  7. Article
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  12. Alzheimer's disease and age-related memory decline (preclinical).Pharmacology, biochemistry, and behavior · 2011
    Review
  13. Article
  14. Pharmacological enhancement of memory and executive functioning in laboratory animals.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2011
    Review
  15. Article
  16. Article
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  18. Review
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 3 institutions in 2 countries.

Alvin V TerryProgram in Clinical and Experimental Therapeutics, CJ-1020 The Medical College of Georgia, University of Georgia College of Pharmacy (Augusta Campus), Augusta, GA 30912, USA. aterry@mail.mcg.edu
Jerry J Buccafusco
Gerd D Bartoszyk
Georgia College & State University · USMerck (Germany) · DEVeterans Health Administration · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

rationaleThe superior cognitive effects of atypical neuroleptics over typical agents reported in the schizophrenia literature are often attributed to the more prominent antagonist activity of the atypical drugs at serotonin 5HT(2A) receptors. However, atypical neuroleptics also have activity at many additional neurotransmitter receptors and few studies have specifically (and prospectively) tested the hypothesis that 5HT(2A) antagonism alone results in enhanced cognitive function.

objectivesThe purpose of this study was to evaluate the selective 5-HT(2A) antagonist, 7-{4-[2-(4-fluoro-phenyl)-ethyl]-piperazine-1-carbonyl}-1H-indole-3-carbonitrile HCl (EMD 281014) in young and aged monkeys in a test designed to assess working memory function.

methodsFour oral doses (0.1, 1.0, 3.0, and 10.0 mg/kg) of EMD 281014 were evaluated in six young adult (mean age=9.2 years) and eight aged rhesus macaques (mean age=24.9 years) trained to perform a computer-assisted delayed matching-to-sample (DMTS) task.

resultsDepending on dose, EMD 281014 improved DMTS accuracy in young and aged monkeys primarily at either the medium or long retention intervals. While the latencies associated with incorrect color selections (choices latencies) tended to be longer than those associated with correct selections (particularly in the aged subjects) under baseline conditions, there were no significant effects of EMD 281014 on either sample or choice latencies in either age group. In addition, no adverse effects were observed across the range of doses evaluated in either cohort of animals.

conclusionThese experiments, conducted in a non-human primate model, suggest that selective 5HT(2A) antagonists such as EMD 281014 could offer therapeutic benefit to younger and older psychiatric patients by improving working memory function.

Indexed as

AgingAnimalsBody WeightConditioning, OperantDose-Response Relationship, DrugFemaleIndolesMacaca mulattaMaleMemory, Short-TermPiperazinesPsychomotor PerformanceReaction TimeReceptor, Serotonin, 5-HT2ASerotonin AntagonistsSex CharacteristicsEMD 281014IndolesPiperazinesReceptor, Serotonin, 5-HT2ASerotonin Antagonists

Identifiers

PMID15619109
OpenAlexW2063392185

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.