Evidence map›Paper›PMID 31739001›Full record

ReviewBehavioural brain research2020

Antidepressant effects of ketamine on depression-related phenotypes and dopamine dysfunction in rodent models of stress.

Millie Rincón-Cortés, Anthony A Grace

Open access · greenAbstract readReview
In one paragraph

Review in Behavioural brain research, 2020. 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
3.3field-weighted citation impact, top 7% 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, 69 citations in OpenAlex.

  1. Article
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  6. Article
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  9. Review
  10. Neuroprotective effects of total phenolics fromFrontiers in pharmacology · 2024
    Article
  11. Article
  12. Article
  13. Review
  14. Antidepressant-like Activity of Patchouli Oil var. Tapak Tuan (Pharmaceuticals (Basel, Switzerland) · 2022
    Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Review
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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

2 authors at 1 institution in 1 country.

Millie Rincón-CortésDepartment of Neuroscience, University of Pittsburgh, Pittsburgh, PA, 15260, United States. Electronic address: rincon-cortes@pitt.edu.
Anthony A GraceDepartment of Neuroscience, University of Pittsburgh, Pittsburgh, PA, 15260, United States; Department of Psychiatry, University of Pittsburgh, Pittsburgh, PA, 15260, United States; Department of Psychology, University of Pittsburgh, Pittsburgh, PA, 15260, United States.
University of Pittsburgh · US

Funding

Gating of Information Flow Within the Nucleus Accumbens (Supplement)R01MH057440 · NIMH · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI ANTHONY A GRACE · 1997 to 2026
$7.2M
Circuit-based Study of Depression/Anhedonia in RatsR01MH101180 · NIMH · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI GRACE, ANTHONY A · 2014 to 2018
$1.9M
Circuit-based study of sex differences in stress-induced dopamine down regulationF32MH110128 · NIMH · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI RINCON CORTES, MILLIE · 2016 to 2017
$101k
NIMH NIH HHS F32 MH110128NIMH NIH HHS R01 MH057440NIMH NIH HHS R01 MH101180
6 · The paper itself

Abstract

Depression, the most prevalent psychiatric disorder, is characterized by increased negative affect (i.e. depressed mood) and reduced positive affect (i.e. anhedonia). Stress is a risk factor for depression in humans, and animal models of chronic stress are typically used to study neurobehavioral alterations relevant to depression. Common behavioral outcomes in rodent models of chronic stress include anhedonia, social dysfunction and behavioral despair. For example, chronically stressed rodents exhibit reduced reward preference, as measured by a loss of preference for sucrose solutions and time spent interacting with a novel conspecific, while also exhibiting less time struggling against inescapable stressors (e.g. forced swim, tail suspension). In both humans and rodents, anhedonia is associated with dysfunction of the dopamine (DA) system. Unlike traditional antidepressants, which are limited by inadequate efficacy and delayed therapeutic response, acute ketamine administration rapidly alleviates depressive symptoms in humans and reverses stress-induced changes in animal models. These effects are partially mediated via actions on the DA system. This review summarizes the clinical effects of ketamine, the neurobiological underpinnings of depression with a focus on DA dysfunction, as well as antidepressant effects of ketamine on depression-related endophenotypes (i.e. anhedonia, despair) and ventral tegmental area (VTA) activity in rodent models of repeated stress. Moreover, we discuss evidence regarding sex differences in ketamine's antidepressant effects, wherein females appear to be more sensitive to lower dose ketamine, as well as novel findings suggesting that ketamine has prophylactic effects with regard to protection against the neurobehavioral impact of future stressors.

Indexed as

DepressionStress, PsychologicalAnhedoniaAnimalsAntidepressive AgentsBehavior, AnimalDisease Models, AnimalDopamineKetamineVentral Tegmental AreaAntidepressive AgentsDopamineKetamineAnhedoniaAnimal modelsDepressionDopamineKetamineStress

Identifiers

PMID31739001
PMCPMC6948930
OpenAlexW2984586476

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.