Evidence map›Paper›PMID 24434869›Full record

ArticleLearning & memory (Cold Spring Harbor, N.Y.)2014

Animal model of methylphenidate's long-term memory-enhancing effects.

Stephanie A Carmack, Kristin K Howell, Kleou Rasaei, Emilie T Reas, Stephan G Anagnostaras

Open access · diamondAbstract read
In one paragraph

Article in Learning & memory (Cold Spring Harbor, N.Y.), 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 2 pooled it
–field-weighted citation impact
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

19 citing papers in PubMed, 2 syntheses or guidelines pooled it, 37 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Alpha-2 Adrenoreceptor Antagonist Yohimbine Potentiates Consolidation of Conditioned Fear.The international journal of neuropsychopharmacology · 2022
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  13. A single dose of cocaine enhances prospective memory performance.Journal of psychopharmacology (Oxford, England) · 2018
    Article
  14. Noradrenergic Modulation of Fear Conditioning and Extinction.Frontiers in behavioral neuroscience · 2018
    Review
  15. Dopamine release from the locus coeruleus to the dorsal hippocampus promotes spatial learning and memory.Proceedings of the National Academy of Sciences of the United States of America · 2016
    Article
  16. 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 1 institution in 1 country.

Stephanie A CarmackMolecular Cognition Laboratory, Department of Psychology, University of California, San Diego, California 92093-0109, USA.
Kristin K Howell
Kleou Rasaei
Emilie T Reas
Stephan G Anagnostaras
University of California, San Diego · US

Funding

Molecular Cognition of AddictionR01DA020041 · NIDA · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI ANAGNOSTARAS, STEPHAN G · 2007 to 2011
$1.5M
NIDA NIH HHS DA020041NIDA NIH HHS R01 DA020041
6 · The paper itself

Abstract

Methylphenidate (MPH), introduced more than 60 years ago, accounts for two-thirds of current prescriptions for attention deficit hyperactivity disorder (ADHD). Although many studies have modeled MPH's effect on executive function, almost none have directly modeled its effect on long-term memory (LTM), even though improvement in LTM is a critical target of therapeutic intervention in ADHD. We examined the effects of a wide range of doses of MPH (0.01-10 mg/kg, i.p.) on Pavlovian fear learning, a leading model of memory. MPH's effects were then compared to those of atomoxetine (0.1-10 mg/kg, i.p.), bupropion (0.5-20 mg/kg, i.p.), and citalopram (0.01-10 mg/kg, i.p.). At low, clinically relevant doses, MPH enhanced fear memory; at high doses it impaired memory. MPH's memory-enhancing effects were not confounded by its effects on locomotion or anxiety. Further, MPH-induced memory enhancement seemed to require both dopamine and norepinephrine transporter inhibition. Finally, the addictive potential of MPH (1 mg/kg and 10 mg/kg) was compared to those of two other psychostimulants, amphetamine (0.005 mg/kg and 1.5 mg/kg) and cocaine (0.15 mg/kg and 15 mg/kg), using a conditioned place preference and behavioral sensitization paradigm. We found that memory-enhancing effects of psychostimulants observed at low doses are readily dissociable from their reinforcing and locomotor activating effects at high doses. Together, our data suggest that fear conditioning will be an especially fruitful platform for modeling the effects of psychostimulants on LTM in drug development.

Indexed as

Adrenergic Uptake InhibitorsAmphetamineAnimalsAtomoxetine HydrochlorideBupropionCentral Nervous System StimulantsCitalopramCocaineConditioning, ClassicalDose-Response Relationship, DrugFearFemaleLocomotionMaleMaze LearningMemory, Long-TermAdrenergic Uptake InhibitorsAmphetamineAtomoxetine HydrochlorideBupropionCentral Nervous System StimulantsCitalopramCocaineMethylphenidateNootropic AgentsPropylaminesSelective Serotonin Reuptake Inhibitors

Identifiers

PMID24434869
PMCPMC3895222
OpenAlexW2048856924

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.