Evidence map›Paper›PMID 22805599›Full record

ArticleNeuropsychopharmacology : official publication of the American College of Neuropsychopharmacology2012

Long-term exposure to oral methylphenidate or dl-amphetamine mixture in peri-adolescent rhesus monkeys: effects on physiology, behavior, and dopamine system development.

Paul L Soto, Kristin M Wilcox, Yun Zhou, Anil Kumar, Nancy A Ator, Mark A Riddle, Dean F Wong, Michael R Weed

Erratum issuedOpen access · bronzeAbstract read
In one paragraph

Article in Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
4.6field-weighted citation impact, top 5% 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

39 citing papers in PubMed, 59 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Article
  5. Methylphenidate as a causal test of translational and basic neural coding hypotheses.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  6. Article
  7. Article
  8. Review
  9. Review
  10. Article
  11. Article
  12. Changes in Endogenous Dopamine Induced by Methylphenidate Predict Functional Connectivity in Nonhuman Primates.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2019
    Article
  13. Review
  14. Article
  15. Article
  16. Linking ADHD to the Neural Circuitry of Attention.Trends in cognitive sciences · 2017
    Review
  17. Article
  18. Article
  19. Regulation of emotional response in juvenile monkeys treated with fluoxetine: MAOA interactions.European neuropsychopharmacology : the journal of the European College of Neuropsychopharmacology · 2016
    Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 1 institution in 1 country.

Paul L SotoDepartment of Psychiatry and Behavioral Sciences, Johns Hopkins School of Medicine, Baltimore, MD, USA.
Kristin M Wilcox
Yun Zhou
Anil Kumar
Nancy A Ator
Mark A Riddle
Dean F Wong
Michael R Weed
Johns Hopkins University · US

Funding

Oral Self-Dosing/Behavioral AssessmentU01MH075378 · NIMH · JOHNS HOPKINS UNIVERSITY · PI ATOR, NANCY A. · 2005 to 2009
$4.1M
NIMH NIH HHS U01 MH075378NIMH NIH HHS U01-MH075378
6 · The paper itself

Abstract

The stimulants methylphenidate and amphetamine are used to treat children with attention deficit/hyperactivity disorder over important developmental periods, prompting concerns regarding possible long-term health impact. This study assessed the effects of such a regimen in male, peri-adolescent rhesus monkeys on a variety of cognitive/behavioral, physiological, and in vivo neurochemical imaging parameters. Twice daily (0900 and 1200 hours), for a total of 18 months, juvenile male monkeys (8 per group) consumed either an unadulterated orange-flavored solution, a methylphenidate solution, or a dl-amphetamine mixture. Doses were titrated to reach blood/plasma levels comparable to therapeutic levels in children. [¹¹C]MPH and [¹¹C]raclopride dynamic PET scans were performed to image dopamine transporter and D₂-like receptors, respectively. Binding potential (BP(ND)), an index of tracer-specific binding, and amphetamine-induced changes in BP(ND) of [¹¹C]raclopride were estimated by kinetic modeling. There were no consistent differences among groups on the vast majority of measures, including cognitive (psychomotor speed, timing, inhibitory control, cognitive flexibility), general activity, physiological (body weight, head circumference, crown-to-rump length), and neurochemical (ie, developmental changes in dopamine transporter, dopamine D₂ receptor density, and amphetamine-stimulated dopamine release were as expected). Cytogenetic studies indicated that neither drug was a clastogen in rhesus monkeys. Thus, methylphenidate and amphetamine at therapeutic blood/plasma levels during peri-adolescence in non-human primates have little effect on physiological or behavioral/cognitive development.

Indexed as

AmphetamineAnimalsBehavior, AnimalCentral Nervous System StimulantsChromosome AberrationsData Interpretation, StatisticalDopamineDopamine Plasma Membrane Transport ProteinsExecutive FunctionGrowthMacaca mulattaMaleMethylphenidateMotor ActivityNervous SystemPositron-Emission TomographyAmphetamineCentral Nervous System StimulantsDopamineDopamine Plasma Membrane Transport ProteinsMethylphenidateReceptors, Dopamine D2

Identifiers

PMID22805599
PMCPMC3473325
OpenAlexW2026985379

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.