Evidence map›Paper›PMID 37586638›Full record

ArticleProgress in neuro-psychopharmacology & biological psychiatry2023

Relationship between two forms of impulsivity in mice at baseline and under acute and sub-chronic atomoxetine treatment.

Maria Kyriakidou, Maitane Caballero-Puntiverio, Jesper T Andreasen, Morgane Thomsen

Open access · hybridAbstract read
In one paragraph

Article in Progress in neuro-psychopharmacology & biological psychiatry, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.4field-weighted citation impact, top 36% 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

0 citing papers in PubMed, 2 citations in OpenAlex.

No citing paper in PubMed yet.

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.

Maria KyriakidouLaboratory of Neuropsychiatry, Psychiatric Centre Copenhagen, Mental Health Services in the Capital Region of Denmark, Copenhagen, Denmark.
Maitane Caballero-PuntiverioDepartment of Drug Design and Pharmacology, University of Copenhagen, Copenhagen, Denmark.
Jesper T AndreasenDepartment of Drug Design and Pharmacology, University of Copenhagen, Copenhagen, Denmark. Electronic address: jta@sund.ku.dk.
Morgane ThomsenLaboratory of Neuropsychiatry, Psychiatric Centre Copenhagen, Mental Health Services in the Capital Region of Denmark, Copenhagen, Denmark; Department of Neuroscience, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
University of Copenhagen · DKCapital Region of Denmark · DK

Funding

Glucagon-like peptide-1 modulation of alcohol effectsR01AA025071 · NIAAA · REGION HOVEDSTADEN · PI THOMSEN, MORGANE HERMANN · 2017 to 2022
$627k
NIAAA NIH HHS R01 AA025071
6 · The paper itself

Abstract

rationaleImpulsivity is a symptom of various mental disorders, including attention deficit hyperactivity disorder (ADHD), bipolar disorder, and addiction. Impulsivity is not a unitary construct, but is present in different forms, yet only a few rodent studies have explored the relationship between these forms within individual subjects.

objectivesIn this study, we compared behaviors representing two impulsivity forms, delay discounting (choice impulsivity) and premature responding (waiting impulsivity), within the same mice.

methodsC57BL/6J male mice were concurrently trained and tested in the delay discounting task and the rodent continuous performance test in a counterbalanced design. The effects of the ADHD medication atomoxetine were tested in both tasks, after both acute (0.3-5.0 mg/kg) and sub-chronic (0.3 mg/kg twice daily for seven days) administration.

resultsThere was no correlation between the two impulsivity forms at baseline. Acute atomoxetine treatment (1, 3, and 5 mg/kg) significantly reduced premature responding. Furthermore, sub-chronic treatment with 0.3 mg/kg of atomoxetine caused a stable decrease in premature responding. Atomoxetine had no significant effect on delay discounting after acute or sub-chronic administration, although the acute administration of 1 mg/kg showed a trend towards increasing delay discounting.

conclusionsThe present results support that delay discounting and premature responding represent two different forms of impulsivity that show dissimilar responses to atomoxetine treatment. The consistency with findings in humans lends support to the translatability of the results in mice.

Indexed as

Attention Deficit Disorder with HyperactivityImpulsive BehaviorAnimalsAtomoxetine HydrochlorideHumansMaleMiceMice, Inbred C57BLRodentiaAtomoxetine HydrochlorideAtomoxetineDelay discountingImpulsivityImpulsivity formsPremature respondingRodent continuous performance test

Identifiers

PMID37586638
PMCPMC11531202
OpenAlexW4385799678

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Registered trials

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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.