Evidence map›Paper›PMID 32061748›Full record

ReviewBehavioural brain research2020

Overlap in the neural circuitry and molecular mechanisms underlying ketamine abuse and its use as an antidepressant.

Saurabh S Kokane, Ross J Armant, Carlos A Bolaños-Guzmán, Linda I Perrotti

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 24 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed, 2 pooled it
5.7field-weighted citation impact, top 3% 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

24 citing papers in PubMed, 2 syntheses or guidelines pooled it, 58 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Efficacy and safety of zuranolone co-initiated with an antidepressant in adults with major depressive disorder: results from the phase 3 CORAL study.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2024
    Trial
  4. Trial
  5. Trial
  6. Ketamine and Evolving Neuroplasticity.Clinical drug investigation · 2026
    Review
  7. Article
  8. Towards an expanded neurocognitive account of ketamine's rapid antidepressant effects.The international journal of neuropsychopharmacology · 2025
    Review
  9. Review
  10. Article
  11. Review
  12. Article
  13. Article
  14. Review
  15. Review
  16. Article
  17. Article
  18. Article
  19. Use and abuse of dissociative and psychedelic drugs in adolescence.Pharmacology, biochemistry, and behavior · 2021
    Review
  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 2 institutions in 1 country.

Saurabh S KokaneDepartment of Psychology, The University of Texas at Arlington, United States.
Ross J ArmantDepartment of Psychology, The University of Texas at Arlington, United States.
Carlos A Bolaños-GuzmánDepartment of Psychological and Brain Sciences, Institute for Neuroscience, Texas A&M University, College Station, TX 77840, United States.
Linda I PerrottiDepartment of Psychology, The University of Texas at Arlington, United States. Electronic address: perrotti@uta.edu.
The University of Texas at Arlington · USTexas A&M University · US

Funding

Serotonin receptors that potentiate addiction-related behavioral and molecular effects induced by methylphenidate plus SSRI exposureR01DA046794 · NIDA · ROSALIND FRANKLIN UNIV OF MEDICINE & SCI · PI BOLANOS, CARLOS A., STEINER, HEINZ · 2019 to 2023
$1.7M
Sex differences cocaine conditioned reward: role of estradiol and intracellular signalingR15DA040809 · NIDA · UNIVERSITY OF TEXAS ARLINGTON · PI PERROTTI, LINDA IRENE · 2016 to 2016
$414k
NIDA NIH HHS R01 DA046794NIDA NIH HHS R15 DA040809
6 · The paper itself

Abstract

Ketamine, a dissociative anesthetic and psychedelic compound, has revolutionized the field of psychopharmacology by showing robust, and rapid-acting antidepressant activity in patients suffering from major depressive disorder (MDD), suicidal tendencies, and treatment-resistant depression (TRD). Ketamine's efficacy, however, is transient, and patients must return to the clinic for repeated treatment as they experience relapse. This is cause for concern because ketamine is known for its abuse liability, and repeated exposure to drugs of abuse often leads to drug abuse/dependence. Though the mechanism(s) underlying its antidepressant activity is an area of current intense research, both clinical and preclinical evidence shows that ketamine's effects are mediated, at least in part, by molecular adaptations resulting in long-lasting synaptic changes in mesolimbic brain regions known to regulate natural and drug reward. This review outlines our limited knowledge of ketamine's neurobiological and biochemical underpinnings mediating its antidepressant effects and correlates them to its abuse potential. Depression and addiction share overlapping neural circuitry and molecular mechanisms, and though speculative, repeated use of ketamine for the treatment of depression could lead to the development of substance use disorder/addiction, and thus should be tempered with caution. There is much that remains to be known about the long-term effects of ketamine, and our lack of understanding of neurobiological mechanisms underlying its antidepressant effects is a clear limiting factor that needs to be addressed systematically before using repeated ketamine in the treatment of depressed patients.

Indexed as

Antidepressive AgentsBrainCholinergic NeuronsDepressive Disorder, Treatment-ResistantExcitatory Amino Acid AntagonistsGABA Agentsgamma-Aminobutyric AcidGlutamic AcidHumansKetamineMajor Depressive DisorderNeural PathwaysNorepinephrineReceptors, GABA-AReceptors, N-Methyl-D-AspartateSerotoninAntidepressive AgentsExcitatory Amino Acid AntagonistsGABA Agentsgamma-Aminobutyric AcidGlutamic AcidKetamineNorepinephrineReceptors, GABA-AReceptors, N-Methyl-D-AspartateSerotoninAddictionBDNFDopamineGlutamatergic neurotransmissionGSK3ΒKetamineMesolimbic doapminergic reward systemmTOR

Identifiers

PMID32061748
PMCPMC7469509
OpenAlexW3005582604

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.