Evidence map›Paper›PMID 33536200›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2021

Reduced Motivation in Perinatal Fluoxetine-Treated Mice: A Hypodopaminergic Phenotype.

Edênia C Menezes, Relish Shah, Lindsay Laughlin, K Yaragudri Vinod, John F Smiley, Catarina Cunha, Andrea Balla, Henry Sershen, Francisco X Castellanos, André Corvelo and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

7 citing papers in PubMed, 10 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

11 authors at 3 institutions in 1 country.

Edênia C MenezesEmotional Brain Institute, Nathan Kline Institute for Psychiatric Research, Orangeburg, New York 10962.
Relish ShahEmotional Brain Institute, Nathan Kline Institute for Psychiatric Research, Orangeburg, New York 10962.
Lindsay LaughlinEmotional Brain Institute, Nathan Kline Institute for Psychiatric Research, Orangeburg, New York 10962.
K Yaragudri VinodEmotional Brain Institute, Nathan Kline Institute for Psychiatric Research, Orangeburg, New York 10962.
John F SmileyEmotional Brain Institute, Nathan Kline Institute for Psychiatric Research, Orangeburg, New York 10962.
Catarina CunhaEmotional Brain Institute, Nathan Kline Institute for Psychiatric Research, Orangeburg, New York 10962.
Andrea BallaDepartment of Neurochemistry, Nathan Kline Institute for Psychiatric Research, Orangeburg, New York 10962.
Henry SershenDepartment of Neurochemistry, Nathan Kline Institute for Psychiatric Research, Orangeburg, New York 10962.
Francisco X CastellanosEmotional Brain Institute, Nathan Kline Institute for Psychiatric Research, Orangeburg, New York 10962.
André CorveloNew York Genome Center, New York, New York 10013.
Cátia M TeixeiraEmotional Brain Institute, Nathan Kline Institute for Psychiatric Research, Orangeburg, New York 10962 catia.teixeira@nki.rfmh.org.
Nathan Kline Institute for Psychiatric Research · USNew York University · USNew York Genome Center · US

Funding

Modulation of serotonin levels during development produce long-lasting changes in dopaminergic functionR01HD095966 · NICHD · NATHAN S. KLINE INSTITUTE FOR PSYCH RES · PI TEIXEIRA, CATIA · 2019 to 2023
$2.0M
Maternal presence modulates pups' brain activity via the serotonergic systemR03HD094978 · NICHD · NATHAN S. KLINE INSTITUTE FOR PSYCH RES · PI TEIXEIRA, CATIA · 2018 to 2019
$162k
NICHD NIH HHS R01 HD095966NICHD NIH HHS R03 HD094978
6 · The paper itself

Abstract

Early life is a sensitive period, in which enhanced neural plasticity allows the developing brain to adapt to its environment. This plasticity can also be a risk factor in which maladaptive development can lead to long-lasting behavioral deficits. Here, we test how early-life exposure to the selective-serotonin-reuptake-inhibitor (SSRI), fluoxetine, affects motivation, and dopaminergic signaling in adulthood. We show for the first time that mice exposed to fluoxetine in the early postnatal period exhibit a reduction in effort-related motivation. These mice also show blunted responses to amphetamine and reduced dopaminergic activation in a sucrose reward task. Interestingly, we find that the reduction in motivation can be rescued in the adult by administering bupropion, a dopamine-norepinephrine reuptake inhibitor used as an antidepressant and a smoke cessation aid but not by fluoxetine. Taken together, our studies highlight the effects of early postnatal exposure of fluoxetine on motivation and demonstrate the involvement of the dopaminergic system in this process.

Indexed as

PhenotypeAnimalsAnimals, NewbornDopamineFemaleFluoxetineLocomotionMaleMiceMice, 129 StrainMice, Inbred C57BLMicrodialysisMotivationSelective Serotonin Reuptake InhibitorsDopamineFluoxetineSelective Serotonin Reuptake Inhibitorsdopaminefluoxetinegestationmotivationpostnatalserotonin

Identifiers

PMID33536200
PMCPMC8018732
OpenAlexW3128923049

What OpenQuestion holds

Textmetadata
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.