Evidence map›Paper›PMID 24452697›Full record

ArticlePsychopharmacology2014

Effects of psychotropic drugs on second messenger signaling and preference for nicotine in juvenile male mice.

Lyonna F Alcantara, Brandon L Warren, Eric M Parise, Sergio D Iñiguez, Carlos A Bolaños-Guzmán

Abstract read
In one paragraph

Article in Psychopharmacology, 2014. 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
0.6field-weighted citation impact, top 33% 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, 23 citations in OpenAlex.

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  10. Enduring effects of adolescent ketamine exposure on cocaine- and sucrose-induced reward in male and female C57BL/6 mice.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2020
    Article
  11. Article
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  14. Functional Upregulation of α4* Nicotinic Acetylcholine Receptors in VTA GABAergic Neurons Increases Sensitivity to Nicotine Reward.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2015
    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

5 authors at 2 institutions in 1 country.

Lyonna F AlcantaraDepartment of Psychology and Program in Neuroscience, Florida State University, 1107 West Call Street, Tallahassee, FL, 32306, USA.
Brandon L Warren
Eric M Parise
Sergio D Iñiguez
Carlos A Bolaños-Guzmán
Florida State University · USCalifornia State University System · 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
Functional studies of antidepressant exposure during adolescence on the brain.SC2GM109811 · NIGMS · UNIVERSITY OF TEXAS EL PASO · PI INIGUEZ, SERGIO DIAZ · 2015 to 2017
$444k
NIDA NIH HHS R01 DA026854NIDA NIH HHS R01DA026854NIGMS NIH HHS SC2 GM109811NIMH NIH HHS T32 MH093311NIMH NIH HHS T32MH093311PHS HHS F31027300
6 · The paper itself

Abstract

rationaleA common treatment strategy for pediatric attention deficit/hyperactivity disorder (ADHD) and major depressive disorder (MDD) is combined methylphenidate (MPH) and fluoxetine (FLX). This has raised concerns because MPH + FLX treatment may have pharmacodynamic properties similar to cocaine, potentially increasing drug abuse liability.

objectivesTo examine the short- and long-term consequences of repeated vehicle, MPH, FLX, MPH + FLX, and cocaine treatment on gene expression in juvenile (postnatal days [PD] 20-34) and adult (PD 70-84) male mice. We further assessed whether juvenile drug treatment influenced subsequent sensitivity for nicotine in adulthood.

methodsJuvenile and adult C57BL/6J mice received vehicle, MPH, FLX, MPH + FLX, or cocaine twice-daily for 15 consecutive days. Mice were sacrificed 24 h or 2 months after the last drug injection to assess drug-induced effects on the extracellular signal-regulated protein kinase-1/2 (ERK) pathway within the ventral tegmental area. Subsequent sensitivity for nicotine (0.05, 0.07, and 0.09 mg/kg) was measured using the place-conditioning paradigm (CPP) 24 h and 2 months after juvenile drug exposure.

resultsMPH + FLX, or cocaine exposure in juvenile mice increased mRNA expression of ERK2 and its downstream targets (CREB, cFos, and Zif268), and increased protein phosphorylation of ERK2 and CREB 2 months after drug exposure. Similar mRNA findings were observed in the adult-treated mice. Findings on gene expression 24 h following drug treatment were variable. Juvenile drug exposure increased preference for nicotine when tested in adulthood.

conclusionsEarly-life MPH + FLX, or cocaine exposure similarly disrupts the ERK pathway, a signaling cascade implicated in motivation and mood regulation, and increases sensitivity for nicotine in adulthood.

Indexed as

AnimalsCocaineConditioning, PsychologicalDopamine Uptake InhibitorsDose-Response Relationship, DrugDrug-Seeking BehaviorFluoxetineGene ExpressionMaleMAP Kinase Signaling SystemMethylphenidateMice, Inbred C57BLNicotineNicotinic AgonistsPsychotropic DrugsRNA, MessengerCocaineDopamine Uptake InhibitorsFluoxetineMethylphenidateNicotineNicotinic AgonistsPsychotropic DrugsRNA, Messenger

Identifiers

PMID24452697
PMCPMC5534174
OpenAlexW2057571684

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.