Evidence map›Paper›PMID 29615190›Full record

ArticleBiological psychiatry2018

Ventral CA3 Activation Mediates Prophylactic Ketamine Efficacy Against Stress-Induced Depressive-like Behavior.

Alessia Mastrodonato, Randy Martinez, Ina P Pavlova, Christina T LaGamma, Rebecca A Brachman, Alfred J Robison, Christine A Denny

Abstract read
In one paragraph

Article in Biological psychiatry, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 58 papers.

0numbers the graph read from it
0cells of the map it votes in
58citing papers in PubMed
2.9field-weighted citation impact, top 8% 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

58 citing papers in PubMed, 97 citations in OpenAlex.

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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

7 authors at 5 institutions in 1 country.

Alessia MastrodonatoDivision of Integrative Neuroscience, Research Foundation for Mental Hygiene/New York State Psychiatric Institute, New York, New York; Department of Psychiatry, Columbia University, New York, New York.
Randy MartinezPaul Smith's College, Paul Smiths, New York.
Ina P PavlovaDivision of Integrative Neuroscience, Research Foundation for Mental Hygiene/New York State Psychiatric Institute, New York, New York.
Christina T LaGammaDivision of Integrative Neuroscience, Research Foundation for Mental Hygiene/New York State Psychiatric Institute, New York, New York.
Rebecca A BrachmanDepartment of Psychiatry, Columbia University, New York, New York.
Alfred J RobisonDepartment of Physiology and Neuroscience Program, Michigan State University, East Lansing, Michigan.
Christine A DennyDivision of Integrative Neuroscience, Research Foundation for Mental Hygiene/New York State Psychiatric Institute, New York, New York; Department of Psychiatry, Columbia University, New York, New York. Electronic address: cad2125@cumc.columbia.edu.
Columbia University · USResearch Foundation For Mental Hygiene · USMichigan State University · USNew York State Psychiatric InstitutePaul Smith's College · US

Funding

Projection-specific gene expression in resilience to chronic stressR01MH111604 · NIMH · MICHIGAN STATE UNIVERSITY · PI Michelle Suzanne Mazei-Robison, ALFRED J ROBISON · 2016 to 2026
$4.9M
Optogenetic dissection of hippocampal circuitry underlying Alzheimers diseaseDP5OD017908 · OD · NEW YORK STATE PSYCHIATRIC INSTITUTE DBA RESEARCH FOUNDATION FOR MENTAL HYGIENE, INC · PI DENNY, CHRISTINE ANN · 2013 to 2017
$2.0M
NIH HHS DP5 OD017908NIMH NIH HHS R01 MH111604
6 · The paper itself

Abstract

backgroundWe previously reported that a single injection of ketamine prior to stress protects against the onset of depressive-like behavior and attenuates learned fear. However, the molecular pathways and brain circuits underlying ketamine-induced stress resilience are still largely unknown.

methodsHere, we tested whether prophylactic ketamine administration altered neural activity in the prefrontal cortex and/or hippocampus. Mice were injected with saline or ketamine (30 mg/kg) 1 week before social defeat. Following behavioral tests assessing depressive-like behavior, mice were sacrificed and brains were processed to quantify ΔFosB expression. In a second set of experiments, mice were stereotaxically injected with viral vectors into ventral CA3 (vCA3) in order to silence or overexpress ΔFosB prior to prophylactic ketamine administration. In a third set of experiments, ArcCreER

resultsProphylactic ketamine administration increased ΔFosB expression in the ventral dentate gyrus and vCA3 of social defeat mice but not of control mice. Transcriptional silencing of ΔFosB activity in vCA3 inhibited prophylactic ketamine efficacy, while overexpression of ΔFosB mimicked and occluded ketamine's prophylactic effects. In ArcCreER

conclusionsOur data indicate that prophylactic ketamine may be protective against a stressor by altering neural activity, specifically the neural ensembles representing an individual stressor in vCA3.

Indexed as

AnimalsBehavior Rating ScaleCA3 Region, HippocampalConditioning, ClassicalDepressionFearFemaleKetamineMaleMiceProto-Oncogene Proteins c-fosStress, PsychologicalFosb protein, mouseKetamineProto-Oncogene Proteins c-fosArcHippocampusKetaminePrefrontal cortexStressΔFosB

Identifiers

PMID29615190
PMCPMC6107435
OpenAlexW2791285903

What OpenQuestion holds

Textmetadata
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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.