Evidence map›Paper›PMID 25643872›Full record

ArticlePharmacology, biochemistry, and behavior2015

Methylphenidate treatment beyond adolescence maintains increased cocaine self-administration in the spontaneously hypertensive rat model of attention deficit/hyperactivity disorder.

Britahny M Baskin, Linda P Dwoskin, Kathleen M Kantak

Open access · greenAbstract read
In one paragraph

Article in Pharmacology, biochemistry, and behavior, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

14 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
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  6. Predicting Substance Use Disorder in ADHD Patients using Long-Short Term Memory Model.2018 IEEE International Conference on Healthcare Informatics Workshops : proceedings : 4-7 June 2018, New York, NY. International Conference on Healthcare Informatics (6th : 2018 : New York, N.Y.). Workshops · 2018
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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 1 country.

Britahny M BaskinDepartment of Psychological and Brain Sciences, Boston University, Boston, MA 02215, USA.. Electronic address: britahny.baskin@gmail.com.
Linda P DwoskinDepartment of Pharmaceutical Sciences, College of Pharmacy, University of Kentucky, Lexington, KY 40536 USA. Electronic address: ldwoskin@email.uky.edu.
Kathleen M KantakDepartment of Psychological and Brain Sciences, Boston University, Boston, MA 02215, USA.. Electronic address: kkantak@bu.edu.
Boston University · USUniversity of Kentucky · US

Funding

COGNITIVE ASPECTS OF ADDICTION-RELATED BEHAVIORR01DA011716 · NIDA · BOSTON UNIVERSITY MEDICAL CAMPUS · PI KANTAK, KATHLEEN M. · 1998 to 2013
$4.8M
NIDA NIH HHS R01 DA011716
6 · The paper itself

Abstract

Past research with the spontaneously hypertensive rat (SHR) model of attention deficit/hyperactivity disorder showed that adolescent methylphenidate treatment enhanced cocaine abuse risk in SHR during adulthood. The acquisition of cocaine self-administration was faster, and cocaine dose-response functions were shifted upward under fixed-ratio and progressive ratio schedules compared to adult SHR that received adolescent vehicle treatment or to control strains that received adolescent methylphenidate treatment. The current study determined if extending treatment beyond adolescence would ameliorate long-term consequences of adolescent methylphenidate treatment on cocaine abuse risk in adult SHR. Treatments (vehicle or 1.5mg/kg/day oral methylphenidate) began on postnatal day 28. Groups of male SHR were treated with vehicle during adolescence and adulthood, with methylphenidate during adolescence and vehicle during adulthood, or with methylphenidate during adolescence and adulthood. The group receiving adolescent-only methylphenidate was switched to vehicle on P56. Cocaine self-administration began on postnatal day 77, and groups receiving methylphenidate during adolescence and adulthood were treated either 1-h before or 1-h after daily sessions. At baseline under a fixed-ratio 1 schedule, cocaine self-administration (2h sessions; 0.3mg/kg unit dose) did not differ among the four treatment groups. Under a progressive ratio schedule (4.5h maximum session length; 0.01-1.0mg/kg unit doses), breakpoints for self-administered cocaine in SHR receiving the adult methylphenidate treatment 1-h pre-session were not different from the vehicle control group. However, compared to the vehicle control group, breakpoints for self-administered cocaine at the 0.3 and 1.0mg/kg unit doses were greater in adult SHR that received adolescent-only methylphenidate or received methylphenidate that was continued into adulthood and administered 1-h post-session. These findings suggest that extending methylphenidate treatment beyond adolescence does not ameliorate explicitly the long-term consequences of adolescent methylphenidate treatment. Pre-session methylphenidate may mask temporarily the detection of an increase in cocaine self-administration following chronic methylphenidate treatment.

Indexed as

Age FactorsAnimalsAttention Deficit Disorder with HyperactivityCentral Nervous System StimulantsCocaine-Related DisordersDisease Models, AnimalDose-Response Relationship, DrugMaleMethylphenidateRatsRats, Inbred SHRCentral Nervous System StimulantsMethylphenidateAdolescenceAttention deficit/hyperactivity disorderCocaineMethylphenidateSelf-administrationSpontaneously hypertensive rat

Identifiers

PMID25643872
PMCPMC4369437
OpenAlexW1995544466

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.