Evidence map›Paper›PMID 32241310›Full record

ReviewPsychological medicine2021

Translating the promise of 5HT

Susannah E Murphy, Angharad N de Cates, Amy L Gillespie, Beata R Godlewska, Jessica C Scaife, Lucy C Wright, Philip J Cowen, Catherine J Harmer

Open access · hybridAbstract readReview
In one paragraph

Review in Psychological medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
2.7field-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

30 citing papers in PubMed, 46 citations in OpenAlex.

  1. Article
  2. Early effects of a novel 5-HTThe British journal of psychiatry : the journal of mental science · 2026
    Article
  3. Article
  4. Article
  5. Article
  6. Prostaglandin FThe Journal of veterinary medical science · 2025
    Article
  7. Combinatorial targeting of NMDARs and 5-HTAlzheimer's research & therapy · 2025
    Article
  8. Chronic, combinatorial targeting of NMDARs and 5-HTNeuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2025
    Article
  9. Article
  10. Review
  11. Article
  12. Review
  13. Review
  14. Effects of a 5-HTScientific reports · 2024
    Article
  15. Article
  16. SSRIs in the Treatment of Depression: A Pharmacological CUL-DE-SAC?Current topics in behavioral neurosciences · 2024
    Review
  17. Article
  18. 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 1 institution in 1 country.

Susannah E MurphyUniversity Department of Psychiatry, Warneford Hospital, University of Oxford, OX3 7JX, UK.
Angharad N de CatesUniversity Department of Psychiatry, Warneford Hospital, University of Oxford, OX3 7JX, UK.
Amy L GillespieUniversity Department of Psychiatry, Warneford Hospital, University of Oxford, OX3 7JX, UK.
Beata R GodlewskaUniversity Department of Psychiatry, Warneford Hospital, University of Oxford, OX3 7JX, UK.
Jessica C ScaifeUniversity Department of Psychiatry, Warneford Hospital, University of Oxford, OX3 7JX, UK.
Lucy C WrightUniversity Department of Psychiatry, Warneford Hospital, University of Oxford, OX3 7JX, UK.
Philip J CowenUniversity Department of Psychiatry, Warneford Hospital, University of Oxford, OX3 7JX, UK.
Catherine J HarmerUniversity Department of Psychiatry, Warneford Hospital, University of Oxford, OX3 7JX, UK.ORCID 0000-0002-1609-8335
Oxford Health NHS Foundation Trust · GB

Funding

Department of HealthMedical Research Council MR/P012604/1Medical Research Council MR/S003037/1
6 · The paper itself

Abstract

Animal experimental studies suggest that 5-HT4 receptor activation holds promise as a novel target for the treatment of depression and cognitive impairment. 5-HT4 receptors are post-synaptic receptors that are located in striatal and limbic areas known to be involved in cognition and mood. Consistent with this, 5-HT4 receptor agonists produce rapid antidepressant effects in a number of animal models of depression, and pro-cognitive effects in tasks of learning and memory. These effects are accompanied by molecular changes, such as the increased expression of neuroplasticity-related proteins that are typical of clinically useful antidepressant drugs. Intriguingly, these antidepressant-like effects have a fast onset of their action, raising the possibility that 5-HT4 receptor agonists may be a particularly useful augmentation strategy in the early stages of SSRI treatment. Until recently, the translation of these effects to humans has been challenging. Here, we review the evidence from animal studies that the 5-HT4 receptor is a promising target for the treatment of depression and cognitive disorders, and outline a potential pathway for the efficient and cost-effective translation of these effects into humans and, ultimately, to the clinic.

Indexed as

AnimalsAntidepressive AgentsDepressionMiceReceptors, Serotonin, 5-HT4Selective Serotonin Reuptake InhibitorsSerotonin 5-HT4 Receptor AgonistsAntidepressive AgentsReceptors, Serotonin, 5-HT4Selective Serotonin Reuptake InhibitorsSerotonin 5-HT4 Receptor AgonistsAntidepressantscognitionemotionserotonin

Identifiers

PMID32241310
PMCPMC8188527
OpenAlexW3014288215

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.