Evidence map›Paper›PMID 37419977›Full record

ArticleNature communications2023

Amphetamine disrupts dopamine axon growth in adolescence by a sex-specific mechanism in mice.

Lauren M Reynolds, Giovanni Hernandez, Del MacGowan, Christina Popescu, Dominique Nouel, Santiago Cuesta, Samuel Burke, Katherine E Savell, Janet Zhao, Jose Maria Restrepo-Lozano and 14 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
4.6field-weighted citation impact, top 4% 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

19 citing papers in PubMed, 31 citations in OpenAlex.

  1. Prefrontal cortex development and its implications in mental illness.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2026
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  16. Social Defeat Stress Model for Adolescent C57BL/6 Male and Female Mice.Journal of visualized experiments : JoVE · 2024
    Article
  17. Article
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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

24 authors at 6 institutions in 3 countries.

Lauren M ReynoldsIntegrated Program in Neuroscience, McGill University, Montréal, QC, Canada.ORCID 0000-0003-3798-2055
Giovanni HernandezDouglas Mental Health University Institute, Montréal, QC, Canada.
Del MacGowanIntegrated Program in Neuroscience, McGill University, Montréal, QC, Canada.
Christina PopescuIntegrated Program in Neuroscience, McGill University, Montréal, QC, Canada.ORCID 0000-0003-1738-4680
Dominique NouelDouglas Mental Health University Institute, Montréal, QC, Canada.
Santiago CuestaDouglas Mental Health University Institute, Montréal, QC, Canada.ORCID 0000-0001-6960-9410
Samuel BurkeCNS Research Group, Department of Pharmacology and Physiology, Department of Neurosciences, Faculty of Medicine, Université de Montréal, Montreal, QC, Canada.
Katherine E SavellDepartment of Neurobiology, University of Alabama at Birmingham, Birmingham, AL, USA.ORCID 0000-0001-8811-8254
Janet ZhaoDouglas Mental Health University Institute, Montréal, QC, Canada.
Jose Maria Restrepo-LozanoIntegrated Program in Neuroscience, McGill University, Montréal, QC, Canada.
Michel GirouxDouglas Mental Health University Institute, Montréal, QC, Canada.
Sonia IsraelDouglas Mental Health University Institute, Montréal, QC, Canada.ORCID 0000-0002-2213-4179
Taylor OrsiniDouglas Mental Health University Institute, Montréal, QC, Canada.
Susan HeDouglas Mental Health University Institute, Montréal, QC, Canada.
Michael WodzinskiDouglas Mental Health University Institute, Montréal, QC, Canada.
Radu G AvramescuDouglas Mental Health University Institute, Montréal, QC, Canada.
Matthew PokinkoIntegrated Program in Neuroscience, McGill University, Montréal, QC, Canada.
Julia G EpelbaumDouglas Mental Health University Institute, Montréal, QC, Canada.
Zhipeng NiuDouglas Mental Health University Institute, Montréal, QC, Canada.
Andrea Harée Pantoja-UrbánIntegrated Program in Neuroscience, McGill University, Montréal, QC, Canada.
Louis-Éric TrudeauCNS Research Group, Department of Pharmacology and Physiology, Department of Neurosciences, Faculty of Medicine, Université de Montréal, Montreal, QC, Canada.ORCID 0000-0003-4684-1377
Bryan KolbCanadian Centre for Behavioural Neuroscience, University of Lethbridge, Lethbridge, AB, Canada.
Jeremy J DayDepartment of Neurobiology, University of Alabama at Birmingham, Birmingham, AL, USA.ORCID 0000-0002-7361-3399
Cecilia FloresDouglas Mental Health University Institute, Montréal, QC, Canada. cecilia.flores@mcgill.ca.ORCID 0000-0001-8606-5910
Douglas Mental Health University Institute · CAUniversité de Montréal · CAUniversity of Alabama at Birmingham · USCentre National de la Recherche Scientifique · FRRutgers, The State University of New Jersey · USUniversity of Lethbridge · CA

Funding

Amphetamine in adolescence disrupts frontal cortex developmentR01DA037911 · NIDA · MCGILL UNIVERSITY · PI FLORES, CECILIA · 2015 to 2024
$2.5M
Amphetamine During Adolescence Reroutes Mesolimbic Dopamine Axons to the Prefrontal Cortex via DCC SignalingF31DA041188 · NIDA · MCGILL UNIVERSITY · PI REYNOLDS, LAUREN MACKENZIE · 2016 to 2018
$99k
NIDA NIH HHS F31 DA041188NIDA NIH HHS R01 DA037911
6 · The paper itself

Abstract

Initiating drug use during adolescence increases the risk of developing addiction or other psychopathologies later in life, with long-term outcomes varying according to sex and exact timing of use. The cellular and molecular underpinnings explaining this differential sensitivity to detrimental drug effects remain unexplained. The Netrin-1/DCC guidance cue system segregates cortical and limbic dopamine pathways in adolescence. Here we show that amphetamine, by dysregulating Netrin-1/DCC signaling, triggers ectopic growth of mesolimbic dopamine axons to the prefrontal cortex, only in early-adolescent male mice, underlying a male-specific vulnerability to enduring cognitive deficits. In adolescent females, compensatory changes in Netrin-1 protect against the deleterious consequences of amphetamine on dopamine connectivity and cognitive outcomes. Netrin-1/DCC signaling functions as a molecular switch which can be differentially regulated by the same drug experience as function of an individual's sex and adolescent age, and lead to divergent long-term outcomes associated with vulnerable or resilient phenotypes.

Indexed as

AmphetamineDopamineAnimalsAxonsDCC ReceptorFemaleMaleMiceNetrin-1AmphetamineDCC ReceptorDopamineNetrin-1

Identifiers

PMID37419977
PMCPMC10329029
OpenAlexW4383499952

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.