Evidence map›Paper›PMID 31927606›Full record

ArticlePsychopharmacology2020

Ketamine induces immediate and delayed alterations of OCD-like behavior.

Summer L Thompson, Amanda C Welch, Julia Iourinets, Stephanie C Dulawa

Abstract read
PubMed Publisher
In one paragraph

Article in Psychopharmacology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.5field-weighted citation impact, top 11% 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

11 citing papers in PubMed, 22 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Increased Compulsivity in Adulthood after Early Adolescence Immune Activation: Preclinical Evidence.International journal of environmental research and public health · 2021
    Article
  10. Serotonin 5-HTPsychopharmacology · 2021
    Article
  11. 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

4 authors at 2 institutions in 1 country.

Summer L ThompsonCommittee on Neurobiology, University of Chicago, Chicago, IL, 60637, USA.
Amanda C WelchDepartment of Psychiatry, University of California San Diego, 9500 Gilman Drive, La Jolla, CA, 92093, USA.
Julia IourinetsUniversity of Rochester School of Medicine and Dentistry, Rochester, NY, 14642, USA.
Stephanie C DulawaDepartment of Psychiatry, University of California San Diego, 9500 Gilman Drive, La Jolla, CA, 92093, USA. sdulawa@ucsd.edu.
University of California, San Diego · USUniversity of Rochester · US

Funding

NEUROPSYCHOPHARMACOLOLGY TRG FOR DRUG ABUSE RESEARCHT32DA007255 · NIDA · UNIVERSITY OF CHICAGO · PI VEZINA, PAUL R · 1991 to 2012
$5.9M
TRAINING IN NEURAL SYSTEMST32GM007839 · NIGMS · UNIVERSITY OF CHICAGO · PI MASON, PEGGY · 1985 to 2012
$4.2M
International Mental Health Research Organization Rising Star Depression Research AwardNational Alliance for Research on Schizophrenia and Depression Independent Investigator AwardNIDA NIH HHS T32 DA07255NIGMS NIH HHS T32 GM07839
6 · The paper itself

Abstract

rationaleObsessive-compulsive disorder (OCD) is a psychiatric disorder characterized by intrusive obsessive thoughts and/or compulsive behaviors. Currently, serotonin reuptake inhibitors (SRIs) provide the only pharmacological monotherapy for OCD, but response rates are insufficient. Ketamine, a noncompetitive NMDA receptor antagonist, was reported to have rapid, sustained therapeutic effects in OCD patients. However, the mechanisms remain unknown.

objectivesHere, we aimed to provide a platform for investigating mechanisms underlying anti-OCD effects of ketamine treatment by assessing whether ketamine pretreatment could alleviate 5-HT1B receptor (5-HT1BR)-induced OCD-like behavior in mice.

methodsWe assessed whether acute ketamine (0, 3, 10, 30 mg/kg), administered at two pretreatment time points (30 min, 24 h), would modulate 5-HT1BR-induced OCD-like behavior in mice. Behavioral measures were perseverative hyperlocomotion in the open field and deficits in prepulse inhibition (PPI) induced by acute pharmacological 5-HT1BR challenge.

resultsThree milligrams per kilogram of ketamine reduced 5-HT1BR-induced perseverative hyperlocomotion, but not PPI deficits, 24 h postinjection. In contrast, higher doses of ketamine were either ineffective (10 mg/kg) or exacerbated (30 mg/kg) 5-HT1BR-induced perseverative hyperlocomotion 30 min postinjection. At 24 h postinjection, 30 mg/kg ketamine reduced perseverative hyperlocomotion across all groups.

conclusionsOur results suggest that the 5-HT1BR-induced model of OCD-like behavior is sensitive to a low dose of ketamine, a potential fast-acting anti-OCD treatment, and may provide a tool for studying mechanisms underlying the rapid therapeutic effects of ketamine in OCD patients.

Indexed as

AnimalsDose-Response Relationship, DrugExcitatory Amino Acid AntagonistsFemaleKetamineMiceMice, Inbred BALB CObsessive-Compulsive DisorderPrepulse InhibitionRandom AllocationSelective Serotonin Reuptake InhibitorsSerotonin 5-HT1 Receptor AgonistsTime FactorsExcitatory Amino Acid AntagonistsKetamineSelective Serotonin Reuptake InhibitorsSerotonin 5-HT1 Receptor Agonists5-HT1BCompulsiveKetamineNMDAOCDPerseverativePrepulse inhibitionRU24969

Identifiers

PMID31927606
OpenAlexW2999019869

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.