Evidence map›Paper›PMID 22049417›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2011

Chronic 5-HT transporter blockade reduces DA signaling to elicit basal ganglia dysfunction.

Emanuela Morelli, Holly Moore, Tahilia J Rebello, Neil Gray, Kelly Steele, Ennio Esposito, Jay A Gingrich, Mark S Ansorge

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
3.0field-weighted citation impact, top 9% 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

22 citing papers in PubMed, 50 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Dopamine, Immunity, and Disease.Pharmacological reviews · 2023
    Review
  5. Article
  6. Review
  7. Article
  8. Serotonin 5-HTPsychopharmacology · 2021
    Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Review
  14. Decreased Incentive Motivation Following Knockout or Acute Blockade of the Serotonin Transporter: Role of the 5-HT2C Receptor.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2016
    Article
  15. Review
  16. Fluoxetine Administration Exacerbates Oral Tremor and Striatal Dopamine Depletion in a Rodent Pharmacological Model of Parkinsonism.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2015
    Article
  17. Article
  18. Monoamine-sensitive developmental periods impacting adult emotional and cognitive behaviors.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2015
    Review
  19. Article
  20. 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

8 authors at 3 institutions in 3 countries.

Emanuela MorelliDivision of Developmental Neuroscience, Department of Psychiatry, Columbia University, New York, New York 10032, USA.
Holly Moore
Tahilia J Rebello
Neil Gray
Kelly Steele
Ennio Esposito
Jay A Gingrich
Mark S Ansorge
Institute of Developmental Physiology · RUColumbia University · USMario Negri Sud Foundation · IT

Funding

Serotonergic Modulation of Brain Development: Genetic and Pharmacologic InfluencP50MH090966 · NIMH · NEW YORK STATE PSYCHIATRIC INSTITUTE DBA RESEARCH FOUNDATION FOR MENTAL HYGIENE, INC · PI POSNER, JONATHAN E · 2010 to 2014
$9.6M
NIMH NIH HHS P50 MH090966
6 · The paper itself

Abstract

Serotonin (5-HT)-selective reuptake inhibitors (SSRIs) are widely administered for the treatment of depression, anxiety, and other neuropsychiatric disorders, but response rates are low, and side effects often lead to discontinuation. Side effect profiles suggest that SSRIs inhibit dopaminergic activity, but mechanistic insight remains scarce. Here we show that in mice, chronic 5-HT transporter (5-HTT) blockade during adulthood but not during development impairs basal ganglia-dependent behaviors in a dose-dependent and reversible fashion. Furthermore, chronic 5-HTT blockade reduces striatal dopamine (DA) content and metabolism. A causal relationship between reduced DA signaling and impaired basal ganglia-dependent behavior is indicated by the reversal of behavioral deficits through L-DOPA administration. Our data suggest that augmentation of DA signaling would reduce side effects and increase efficacies of SSRI-based therapy.

Indexed as

3,4-Dihydroxyphenylacetic AcidAge FactorsAnimalsAnimals, NewbornBasal GangliaCell CountChromatography, High Pressure LiquidDopamineDopamine AgentsDose-Response Relationship, DrugDrug Administration ScheduleDrug InteractionsExploratory BehaviorFluoxetineHomovanillic AcidLevodopa3,4-Dihydroxyphenylacetic AcidDopamineDopamine AgentsFluoxetineHomovanillic AcidLevodopaSelective Serotonin Reuptake InhibitorsSerotoninSerotonin Plasma Membrane Transport Proteins

Identifiers

PMID22049417
PMCPMC3758550
OpenAlexW1978525638

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.