Evidence map›Paper›PMID 38198569›Full record

ArticleScience translational medicine2024

Rapid-acting antidepressant drugs modulate affective bias in rats.

Justyna K Hinchcliffe, Sarah A Stuart, Christian M Wood, Julia Bartlett, Katie Kamenish, Roberto Arban, Christopher W Thomas, Aslihan Selimbeyoglu, Shaun Hurley, Bastian Hengerer and 2 more

Open access · hybridAbstract read
In one paragraph

Article in Science translational medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
15.3field-weighted citation impact, top 1% 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

12 citing papers in PubMed, 24 citations in OpenAlex.

  1. Trial
  2. Psychedelics produce enduring enhancement of reward responsiveness in male rats.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2026
    Article
  3. Review
  4. Article
  5. Comparing affective bias modification by first- and second-generation antidepressants in male rats using a translational behavioural task.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2026
    Article
  6. Review
  7. Article
  8. Article
  9. Review
  10. Examining memory reconsolidation as a mechanism of nitrous oxide's antidepressant action.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2025
    Review
  11. Review
  12. Effects of psilocybin on uncertain punishment learning.Neurobiology of learning and memory · 2024
    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

12 authors at 4 institutions in 3 countries.

Justyna K HinchcliffeSchool of Physiology, Pharmacology and Neuroscience, University of Bristol, Biomedical Sciences Building, Bristol BS8 1TD, UK.ORCID 0000-0002-9069-5023
Sarah A StuartSchool of Physiology, Pharmacology and Neuroscience, University of Bristol, Biomedical Sciences Building, Bristol BS8 1TD, UK.ORCID 0000-0002-8465-2692
Christian M WoodDepartment of Physiology, Development and Neuroscience, University of Cambridge, Cambridge CB3 2DY, UK.ORCID 0000-0003-1267-5032
Julia BartlettSchool of Physiology, Pharmacology and Neuroscience, University of Bristol, Biomedical Sciences Building, Bristol BS8 1TD, UK.
Katie KamenishSchool of Physiology, Pharmacology and Neuroscience, University of Bristol, Biomedical Sciences Building, Bristol BS8 1TD, UK.ORCID 0009-0008-8660-6754
Roberto ArbanCNS Diseases Research, Boehringer Ingelheim GmbH & Co. KG, Biberach an der Riss, Germany.
Christopher W ThomasCOMPASS Pathways plc, London W1F 0DQ, UK.ORCID 0000-0001-5371-7257
Aslihan SelimbeyogluCOMPASS Pathways plc, London W1F 0DQ, UK.
Shaun HurleyCOMPASS Pathways plc, London W1F 0DQ, UK.ORCID 0009-0007-4173-1669
Bastian HengererCNS Diseases Research, Boehringer Ingelheim GmbH & Co. KG, Biberach an der Riss, Germany.ORCID 0000-0002-7811-9795
Gary GilmourCOMPASS Pathways plc, London W1F 0DQ, UK.ORCID 0000-0003-1777-6975
Emma S J RobinsonSchool of Physiology, Pharmacology and Neuroscience, University of Bristol, Biomedical Sciences Building, Bristol BS8 1TD, UK.ORCID 0000-0002-1299-6541
University of Bristol · GBPathways Behavioral Services · USBoehringer Ingelheim (Germany) · DEUniversity of Cambridge · GB

Funding

Biotechnology and Biological Sciences Research Council BB/N015762/1Biotechnology and Biological Sciences Research Council BB/V015028/1Medical Research Council MR/L011212/1
6 · The paper itself

Abstract

How rapid-acting antidepressants (RAADs), such as ketamine, induce immediate and sustained improvements in mood in patients with major depressive disorder (MDD) is poorly understood. A core feature of MDD is the prevalence of cognitive processing biases associated with negative affective states, and the alleviation of negative affective biases may be an index of response to drug treatment. Here, we used an affective bias behavioral test in rats, based on an associative learning task, to investigate the effects of RAADs. To generate an affective bias, animals learned to associate two different digging substrates with a food reward in the presence or absence of an affective state manipulation. A choice between the two reward-associated digging substrates was used to quantify the affective bias generated. Acute treatment with the RAADs ketamine, scopolamine, or psilocybin selectively attenuated a negative affective bias in the affective bias test. Low, but not high, doses of ketamine and psilocybin reversed the valence of the negative affective bias 24 hours after RAAD treatment. Only treatment with psilocybin, but not ketamine or scopolamine, led to a positive affective bias that was dependent on new learning and memory formation. The relearning effects of ketamine were dependent on protein synthesis localized to the rat medial prefrontal cortex and could be modulated by cue reactivation, consistent with experience-dependent neural plasticity. These findings suggest a neuropsychological mechanism that may explain both the acute and sustained effects of RAADs, potentially linking their effects on neural plasticity with affective bias modulation in a rodent model.

Indexed as

KetamineMajor Depressive DisorderAnimalsAntidepressive AgentsBiasHumansPsilocybinRatsScopolamineAntidepressive AgentsKetaminePsilocybinScopolamine

Identifiers

PMID38198569
PMCPMC7615567
OpenAlexW4390691843

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.