Evidence map›Paper›PMID 31419519›Full record

ReviewBehavioural brain research2019

Rodent ketamine depression-related research: Finding patterns in a literature of variability.

Andrew J Polis, Paul J Fitzgerald, Pho J Hale, Brendon O Watson

Open access · hybridAbstract readReview
In one paragraph

Review in Behavioural brain research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

35 citing papers in PubMed, 58 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Rapid hippocampal synaptic potentiation induced by ketamine metabolite (2R,6R)-hydroxynorketamine persistently primes synaptic plasticity.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2025
    Article
  10. Article
  11. Frontal Alpha Asymmetry and Its Modulation by Monoaminergic Neurotransmitters in Depression.Clinical psychopharmacology and neuroscience : the official scientific journal of the Korean College of Neuropsychopharmacology · 2024
    Review
  12. Article
  13. Article
  14. Article
  15. Therapeutic mechanisms of psychedelics and entactogens.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2024
    Review
  16. Article
  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

4 authors at 1 institution in 1 country.

Andrew J PolisUniversity of Michigan, Department of Psychiatry, Ann Arbor, MI 48109-5720, United States of America.
Paul J FitzgeraldUniversity of Michigan, Department of Psychiatry, Ann Arbor, MI 48109-5720, United States of America.
Pho J HaleUniversity of Michigan, Department of Psychiatry, Ann Arbor, MI 48109-5720, United States of America.
Brendon O WatsonUniversity of Michigan, Department of Psychiatry, Ann Arbor, MI 48109-5720, United States of America. Electronic address: brendonw@umich.edu.
University of Michigan–Ann Arbor · US

Funding

Role of waking activity in determining sleep-based modification of cortical circuitsK08MH107662 · NIMH · WEILL MEDICAL COLL OF CORNELL UNIV · PI WATSON, BRENDON O · 2015 to 2018
$697k
NIMH NIH HHS K08 MH107662
6 · The paper itself

Abstract

Discovering that the anesthetic drug ketamine has rapidly acting antidepressant effects in many individuals with major depression is one of the most important findings in clinical psychopharmacology in recent decades. The initial report of these effects in human subjects was based on a foundation of rodent preclinical studies carried out in the 1990s, and subsequent investigation has included both further studies in individuals with depression, as well as reverse translational experiments in animal models, especially rodents. While there is general agreement in the rodent literature that ketamine has rapidly-acting, and generally sustained, antidepressant-like properties, there are also points of contention across studies, including the precise mechanism of action of this drug. In this review, we briefly summarize prominent yet variable findings regarding the mechanism of action. We also discuss a combination of similarities and variances in the rodent literature in the antidepressant-like effects of ketamine as a function of dose, species and strain, test, stressor, and presumably sex of the experimenter. We then present previously unpublished mouse strain comparison data suggesting that subanesthetic ketamine does not have robust antidepressant-like properties in unstressed animals, and may actually promote depression-like behavior, in contrast to widely reported findings. We conclude that the data best support the notion of ketamine action principally via NMDA receptor antagonism, transiently boosting glutamatergic (and possibly other) signaling in diverse brain circuits. We also suggest that future studies should address in greater detail the extent to which antidepressant-like properties of this drug are stress-sensitive, in an effort to better model major depression present in humans.

Indexed as

AnimalsAntidepressive AgentsDepressionDisease Models, AnimalHumansKetamineMajor Depressive DisorderReceptors, N-Methyl-D-AspartateRodentiaAntidepressive AgentsKetamineReceptors, N-Methyl-D-Aspartate

Identifiers

PMID31419519
PMCPMC6783386
OpenAlexW2968746826

What OpenQuestion holds

Textmetadata
LicenceTDM
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.