Evidence map›Paper›PMID 24968775›Full record

ReviewProgress in brain research2014

Life-long consequences of juvenile exposure to psychotropic drugs on brain and behavior.

Heinz Steiner, Brandon L Warren, Vincent Van Waes, Carlos A Bolaños-Guzmán

Abstract readReview
In one paragraph

Review in Progress in brain research, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
8.7field-weighted citation impact, top 2% 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

9 citing papers in PubMed, 22 citations in OpenAlex.

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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

4 authors at 2 institutions in 1 country.

Heinz SteinerDepartment of Cellular and Molecular Pharmacology, The Chicago Medical School, Rosalind Franklin University of Medicine and Science, North Chicago, IL, USA. Electronic address: heinz.steiner@rosalindfranklin.edu.
Brandon L WarrenDepartment of Psychology and Program in Neuroscience, Florida State University, Tallahassee, FL, USA.
Vincent Van WaesDepartment of Cellular and Molecular Pharmacology, The Chicago Medical School, Rosalind Franklin University of Medicine and Science, North Chicago, IL, USA.
Carlos A Bolaños-GuzmánDepartment of Psychology and Program in Neuroscience, Florida State University, Tallahassee, FL, USA.
Florida State University · USRosalind Franklin University of Medicine and Science · US

Funding

Integrated Clinical Neuroscience Training for Translational ResearchT32MH093311 · NIMH · FLORIDA STATE UNIVERSITY · PI LISA A ECKEL, Pamela K. Keel · 2012 to 2026
$2.3M
Ontogeny of Drug Exposure and Mood Dysregulation.R01DA026854 · NIDA · FLORIDA STATE UNIVERSITY · PI BOLANOS, CARLOS A. · 2010 to 2014
$1.6M
BASAL GANGLIA OUTPUT AND PSYCHOSTIMULANT ABUSER01DA011261 · NIDA · ROSALIND FRANKLIN UNIV OF MEDICINE &SCI · PI STEINER, HEINZ · 2005 to 2009
$1.3M
Risk of cocaine addiction after methylphenidate plus SSRI combination treatmentR21DA031916 · NIDA · UNIVERSITY OF TEXAS AT AUSTIN · PI MARINELLI, MICHELA (MICKY) · 2012 to 2013
$416k
OPIOID PEPTIDES AND COCAINE ABUSER29DA011261 · NIDA · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI STEINER, HEINZ · 1998 to 2002
$306k
NIDA NIH HHS DA011261NIDA NIH HHS DA026854NIDA NIH HHS DA031916NIDA NIH HHS R01 DA011261NIDA NIH HHS R01 DA026854NIDA NIH HHS R21 DA031916NIDA NIH HHS R29 DA011261NIMH NIH HHS MH093311NIMH NIH HHS T32 MH093311
6 · The paper itself

Abstract

Psychostimulants such as methylphenidate (MPH) and antidepressants such as fluoxetine (FLX) are widely used in the treatment of various mental disorders or as cognitive enhancers. These medications are often combined, for example, to treat comorbid disorders. There is a considerable body of evidence from animal models indicating that individually these psychotropic medications can have detrimental effects on the brain and behavior, especially when given during sensitive periods of brain development. However, almost no studies investigate possible interactions between these drugs. This is surprising given that their combined neurochemical effects (enhanced dopamine and serotonin neurotransmission) mimic some effects of illicit drugs such as cocaine and amphetamine. Here, we summarize recent studies in juvenile rats on the molecular effects in the mid- and forebrain and associated behavioral changes, after such combination treatments. Our findings indicate that these combined MPH+FLX treatments can produce similar molecular changes as seen after cocaine exposure while inducing behavioral changes indicative of dysregulated mood and motivation, effects that often endure into adulthood.

Indexed as

AgingAnimalsBehavior, AnimalBrainChildDisease Models, AnimalFluoxetineHumansMethylphenidatePsychotropic DrugsFluoxetineMethylphenidatePsychotropic Drugsaddictiondopaminefluoxetinegene regulationmethylphenidatemoodrewardserotoninstriatumventral tegmental area

Identifiers

PMID24968775
PMCPMC4331026
OpenAlexW1757973043

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.