Evidence map›Paper›PMID 26657171›Full record

ArticlePharmacology, biochemistry, and behavior2016

Adolescent methylphenidate treatment differentially alters adult impulsivity and hyperactivity in the Spontaneously Hypertensive Rat model of ADHD.

S S Somkuwar, K M Kantak, M T Bardo, L P Dwoskin

Open access · greenAbstract read
In one paragraph

Article in Pharmacology, biochemistry, and behavior, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 1 pooled it
1.9field-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

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

  1. Pooled it
  2. Review
  3. Review
  4. Review
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. 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 2 institutions in 1 country.

S S SomkuwarDepartment of Pharmaceutical Sciences, University of Kentucky, Lexington, KY 40536, USA.
K M KantakDepartment of Psychological and Brain Sciences, Boston University, Boston, MA 02215, USA.
M T BardoDepartment of Psychology, University of Kentucky, Lexington, KY 40536, USA.
L P DwoskinDepartment of Pharmaceutical Sciences, University of Kentucky, Lexington, KY 40536, USA. Electronic address: ldwoskin@email.uky.edu.
University of Kentucky · USBoston University · US

Funding

Training and Pilot CoreP50DA005312 · NIDA · UNIVERSITY OF KENTUCKY · PI MILICH, RICHARD · 1987 to 2016
$19.5M
COGNITIVE ASPECTS OF ADDICTION-RELATED BEHAVIORR01DA011716 · NIDA · BOSTON UNIVERSITY MEDICAL CAMPUS · PI KANTAK, KATHLEEN M. · 1998 to 2013
$4.8M
NIDA NIH HHS P50 DA005312NIDA NIH HHS P50 DA05312NIDA NIH HHS R01 DA011716
6 · The paper itself

Abstract

Impulsivity and hyperactivity are two facets of attention deficit/hyperactivity disorder (ADHD). Impulsivity is expressed as reduced response inhibition capacity, an executive control mechanism that prevents premature execution of an intermittently reinforced behavior. During methylphenidate treatment, impulsivity and hyperactivity are decreased in adolescents with ADHD, but there is little information concerning levels of impulsivity and hyperactivity in adulthood after adolescent methylphenidate treatment is discontinued. The current study evaluated impulsivity, hyperactivity as well as cocaine sensitization during adulthood after adolescent methylphenidate treatment was discontinued in the Spontaneously Hypertensive Rat (SHR) model of ADHD. Treatments consisted of oral methylphenidate (1.5mg/kg) or water vehicle provided Monday-Friday from postnatal days 28-55. During adulthood, impulsivity was measured in SHR and control strains (Wistar Kyoto and Wistar rats) using differential reinforcement of low rate (DRL) schedules. Locomotor activity and cocaine sensitization were measured using the open-field assay. Adult SHR exhibited decreased efficiency of reinforcement under the DRL30 schedule and greater levels of locomotor activity and cocaine sensitization compared to control strains. Compared to vehicle, methylphenidate treatment during adolescence reduced hyperactivity in adult SHR, maintained the lower efficiency of reinforcement, and increased burst responding under DRL30. Cocaine sensitization was not altered following adolescent methylphenidate in adult SHR. In conclusion, adolescent treatment with methylphenidate followed by discontinuation in adulthood had a positive benefit by reducing hyperactivity in adult SHR rats; however, increased burst responding under DRL compared to SHR given vehicle, i.e., elevated impulsivity, constituted an adverse consequence associated with increased risk for cocaine abuse liability.

Indexed as

Disease Models, AnimalAgingAnimalsAttention Deficit Disorder with HyperactivityCentral Nervous System StimulantsMaleMethylphenidateRatsRats, Inbred SHRRats, Inbred WKYRats, WistarCentral Nervous System StimulantsMethylphenidateAttention deficit/hyperactivity disorderDifferential reinforcement of low rates scheduleImpulsivityMethylphenidateSpontaneously Hypertensive Rat

Identifiers

PMID26657171
PMCPMC4764879
OpenAlexW2183390437

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.