Evidence map›Paper›PMID 23790225›Full record

ArticleBiological psychiatry2013

Repeated ketamine exposure induces an enduring resilient phenotype in adolescent and adult rats.

Eric M Parise, Lyonna F Alcantara, Brandon L Warren, Katherine N Wright, Roey Hadad, Omar K Sial, Kyle G Kroeck, Sergio D Iñiguez, Carlos A Bolaños-Guzmán

Open access · bronzeAbstract read
In one paragraph

Article in Biological psychiatry, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 61 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
61citing papers in PubMed, 4 pooled it
1.9field-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

61 citing papers in PubMed, 4 syntheses or guidelines pooled it, 124 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Pooled it
  5. Article
  6. Ketamine or Esketamine in Special Populations of Patients With Treatment-Resistant Depression.Medical science monitor : international medical journal of experimental and clinical research · 2026
    Review
  7. Review
  8. Article
  9. The antipsychotic potential ofIBRO neuroscience reports · 2024
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1 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 1 institution in 1 country.

Eric M PariseDepartment of Psychology and Program in Neuroscience, Florida State University, Tallahassee, Florida.
Lyonna F Alcantara
Brandon L Warren
Katherine N Wright
Roey Hadad
Omar K Sial
Kyle G Kroeck
Sergio D Iñiguez
Carlos A Bolaños-Guzmán
Florida State University · US

Funding

Integrated Clinical Neuroscience Training for Translational ResearchT32MH093311 · NIMH · FLORIDA STATE UNIVERSITY · PI LISA A ECKEL, Pamela K. Keel · 2012 to 2026
$2.3M
Ontogeny of Drug Exposure and Mood Dysregulation.R01DA026854 · NIDA · FLORIDA STATE UNIVERSITY · PI BOLANOS, CARLOS A. · 2010 to 2014
$1.6M
Ontogeny of Physical versus Emotional Stress and Reward PathwaysR21DA022351 · NIDA · FLORIDA STATE UNIVERSITY · PI BOLANOS, CARLOS A. · 2008 to 2009
$374k
Long-Term Consequences of Antidepressant Exposure During Adolescence in Male RatsF31DA027300 · NIDA · FLORIDA STATE UNIVERSITY · PI INIGUEZ, SERGIO DIAZ · 2009 to 2011
$80k
NIDA NIH HHS F31 DA027300NIDA NIH HHS F31DA027300NIDA NIH HHS R01 DA026854NIDA NIH HHS R01DA026854NIDA NIH HHS R21 DA022351NIDA NIH HHS R21DA022351NIMH NIH HHS T32 MH093311NIMH NIH HHS T32MH093311
6 · The paper itself

Abstract

backgroundMajor depressive disorder afflicts up to 10% of adolescents. However, nearly 50% of those afflicted are considered nonresponsive to available treatments. Ketamine, a noncompetitive N-methyl-D-aspartate receptor antagonist has shown potential as a rapid-acting and long-lasting treatment for major depressive disorder in adults. Thus, the effectiveness and functional consequences of ketamine exposure during adolescence were explored.

methodsAdolescent male rats (postnatal day [PD] 35) received two ketamine (0, 5, 10, or 20 mg/kg) injections, 4 hours apart, after exposure to day 1 of the forced swim test (FST). The next day, rats were reexposed to the FST to assess ketamine-induced antidepressant-like responses. Separate groups were exposed to chronic unpredictable stress to confirm findings from the FST. After these initial experiments, adolescent naive rats were exposed to either 1 or 15 consecutive days (PD35-49) of ketamine (20 mg/kg) twice daily. Ketamine's influence on behavioral reactivity to rewarding (i.e., sucrose preference) and aversive (i.e., elevated plus-maze, FST) circumstances was then assessed 2 months after treatment. To control for age-dependent effects, adult rats (PD75-89) were exposed to identical experimental conditions.

resultsKetamine (20 mg/kg) reversed the chronic unpredictable stress-induced depression-like behaviors in the FST. Repeated ketamine exposure resulted in anxiolytic- and antidepressant-like responses 2 months after drug exposure. None of the ketamine doses used were capable of inducing drug-seeking behaviors as measured by place preference conditioning.

conclusionsRepeated ketamine exposure induces enduring resilient-like responses regardless of age of exposure. These findings point to ketamine, and its repeated exposure, as a potentially useful antidepressant during adolescence.

Indexed as

Age FactorsAnimalsAntidepressive AgentsAnxietyDepressionExcitatory Amino Acid AntagonistsKetamineMalePhenotypeRatsRats, Sprague-DawleyStress, PsychologicalSwimmingAntidepressive AgentsExcitatory Amino Acid AntagonistsKetamineAdolescenceanxietydepressionketamineratsresiliencestress

Identifiers

PMID23790225
PMCPMC3785550
OpenAlexW1992784372

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.