Evidence map›Paper›PMID 26888470›Full record

ArticleScientific reports2016

Hedonic sensitivity to low-dose ketamine is modulated by gonadal hormones in a sex-dependent manner.

Samantha K Saland, Kristofer J Schoepfer, Mohamed Kabbaj

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06957704 (Evaluation of the Efficacy and Safety of Subcutaneous Ketamine in the Treatment of Depressive Episode With Suicidal Ideation and/or Behavior in Adolescents), which is not on this map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
1.4field-weighted citation impact, top 23% 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.

NCT06957704 phase3not yet recruitingnot on this mapstarted 2025, after this paper: background citation

Evaluation of the Efficacy and Safety of Subcutaneous Ketamine in the Treatment of Depressive Episode With Suicidal Ideation and/or Behavior in Adolescents

TypeinterventionalSponsorFederal University of São PauloRan2025 to 2028Enrolled60ConditionsDepressive Disorder, Suicidal IdeasArmsketamine, Midazolam
3 · Its place in the literature

Who cites it

33 citing papers in PubMed, 55 citations in OpenAlex.

  1. Sex-dependent metabolism of ketamine and (Journal of psychopharmacology (Oxford, England) · 2022
    Trial
  2. Trial
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. The Role of Glutamate Underlying Treatment-resistant Depression.Clinical psychopharmacology and neuroscience : the official scientific journal of the Korean College of Neuropsychopharmacology · 2023
    Review
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
  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

3 authors at 1 institution in 1 country.

Samantha K SalandDepartment of Biomedical Sciences, Program in Neurosciences, College of Medicine, Florida State University, USA.
Kristofer J SchoepferDepartment of Biomedical Sciences, Program in Neurosciences, College of Medicine, Florida State University, USA.
Mohamed KabbajDepartment of Biomedical Sciences, Program in Neurosciences, College of Medicine, Florida State University, USA.
Florida State University · US

Funding

Sex Differences in Ketamine Antidepressant EffectsR01MH099085 · NIMH · FLORIDA STATE UNIVERSITY · PI KABBAJ, MOHAMED, ZHOU, YI · 2013 to 2017
$1.9M
Sex Differences In Anxiety: Role of Zif268R01MH087583 · NIMH · FLORIDA STATE UNIVERSITY · PI KABBAJ, MOHAMED · 2010 to 2014
$1.8M
NIMH NIH HHS R01 MH087583NIMH NIH HHS R01 MH099085NIMH NIH HHS R01 MH87583
6 · The paper itself

Abstract

We recently reported a greater sensitivity of female rats to rapid antidepressant-like effects of ketamine compared to male rats, and that ovarian-derived estradiol (E2) and progesterone (P4) are essential for this response. However, to what extent testosterone may also contribute, and whether duration of response to ketamine is modulated in a sex- and hormone-dependent manner remains unclear. To explore this, we systematically investigated the influence of testosterone, estradiol and progesterone on initiation and maintenance of hedonic response to low-dose ketamine (2.5 mg/kg) in intact and gonadectomized male and female rats. Ketamine induced a sustained increase in sucrose preference of female, but not male, rats in an E2P4-dependent manner. Whereas testosterone failed to alter male treatment response, concurrent administration of P4 alone in intact males enhanced hedonic response low-dose ketamine. Treatment responsiveness in female rats only was associated with greater hippocampal BDNF levels, but not activation of key downstream signaling effectors. We provide novel evidence supporting activational roles for ovarian-, but not testicular-, derived hormones in mediating hedonic sensitivity to low-dose ketamine in female and male rats, respectively. Organizational differences may, in part, account for the persistence of sex differences following gonadectomy and selective involvement of BDNF in treatment response.

Indexed as

Sex CharacteristicsAnimalsBrain-Derived Neurotrophic FactorEstradiolFeeding BehaviorFemaleHippocampusKetamineMaleProgesteroneRatsRats, Sprague-DawleyTestosteroneBrain-Derived Neurotrophic FactorEstradiolKetamineProgesteroneTestosterone

Identifiers

PMID26888470
PMCPMC4766854
OpenAlexW2410881212

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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.