Evidence map›Paper›PMID 30116006›Full record

Trial reportNeuropsychopharmacology : official publication of the American College of Neuropsychopharmacology2019

High-dose ondansetron reduces activation of interoceptive and sensorimotor brain regions.

Emily R Stern, Rebbia Shahab, Stephanie J Grimaldi, Evan Leibu, James W Murrough, Lazar Fleysher, Michael K Parides, Barbara J Coffey, Katherine E Burdick, Wayne K Goodman

Open access · bronzeAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 2 pooled it
1.8field-weighted citation impact, top 15% 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

15 citing papers in PubMed, 2 syntheses or guidelines pooled it, 28 citations in OpenAlex.

  1. Serotonin type 3 receptor (5-HTNeuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2026
    Pooled it
  2. Selective 5HT3 antagonists and sensory processing: a systematic review.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2022
    Pooled it
  3. Trial
  4. Article
  5. Review
  6. Review
  7. Article
  8. Article
  9. Review
  10. Observational
  11. Pharmacotherapeutic Strategies and New Targets in OCD.Current topics in behavioral neurosciences · 2021
    Review
  12. Review
  13. Review
  14. Article
  15. 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

10 authors at 7 institutions in 1 country.

Emily R SternDepartment of Psychiatry, The New York University School of Medicine, New York, NY, USA. emily.stern@nyumc.org.
Rebbia ShahabDepartment of Psychiatry, The New York University School of Medicine, New York, NY, USA.
Stephanie J GrimaldiDepartment of Psychology, Hofstra University, Hempstead, NY, USA.
Evan LeibuDepartment of Psychiatry, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
James W MurroughDepartment of Psychiatry, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Lazar FleysherDepartment of Radiology, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Michael K ParidesDepartment of Population Health Science and Policy, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Barbara J CoffeyDepartment of Psychiatry, University of Miami Medical School, Miami, FL, USA.
Katherine E BurdickDepartment of Psychiatry, Brigham and Women's Hospital, Boston, MA, USA.
Wayne K GoodmanDepartment of Psychiatry, Baylor College of Medicine, Houston, TX, USA.
Icahn School of Medicine at Mount Sinai · USBaylor College of Medicine · USBrigham and Women's Hospital · USHofstra University · USNathan Kline Institute for Psychiatric Research · USNew York University · USUniversity of Miami · US

Funding

The effects of ondansetron on neural systems and symptoms associated with sensory phenomenaR33MH107589 · NIMH · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI STERN, EMILY R · 2017 to 2019
$1.4M
The effects of ondansetron on neural systems and symptoms associated with sensory phenomenaR21MH107589 · NIMH · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI STERN, EMILY R · 2015 to 2016
$922k
NIMH NIH HHS R21 MH107589NIMH NIH HHS R33 MH107589U.S. Department of Health & Human Services | NIH | National Institute of Mental Health (NIMH) R21MH107589
6 · The paper itself

Abstract

Several psychiatric disorders involve abnormalities of interoception and associated neural circuitry centered on the insula. The development of interventions modulating interoceptive circuits could lead to novel treatment approaches for these disorders. The 5-HT3 receptor antagonist ondansetron is a good candidate for the modulation of interoceptive circuits, as 5-HT3 receptors are located abundantly on sensory pathways and ondansetron has shown some clinical utility in disorders characterized by sensory and interoceptive abnormalities. The present study tested the ability of three different doses of ondansetron to engage neural regions involved in interoception to determine the drug's utility as a therapeutic agent to target circuit abnormalities in patients. Fifty-three healthy subjects were randomized to receive a single 8-mg (n = 18), 16-mg (n = 17), or 24-mg (n = 18) dose of ondansetron and placebo before MRI scanning on separate days. Subjects performed an fMRI task previously shown to engage interoceptive circuitry in which they viewed videos depicting body movements/sensation and control videos. The results revealed a highly significant relationship between dosage and activation in bilateral insula, somatosensory and premotor regions, cingulate cortex, and temporal cortex for control but not body-focused videos. These effects were driven by a robust reduction in activation for ondansetron compared to placebo for the 24-mg group, with weaker effects for the 16-mg and 8-mg groups. In conclusion, high-dose ondansetron reduces activation of several areas important for interoception, including insula and sensorimotor cortical regions. This study reveals the potential utility of this drug in modulating hyperactivity in these regions in patients.

Indexed as

AdultBrainFemaleHumansInteroceptionMagnetic Resonance ImagingMaleOndansetronSerotonin AntagonistsYoung AdultOndansetronSerotonin Antagonists

Identifiers

PMID30116006
PMCPMC6300545
OpenAlexW2885869118

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.