Translating the immediate effects of S-Ketamine using hippocampal subfield analysis in healthy subjects-results of a randomized controlled trial

Abstract Antidepressant doses of ketamine rapidly facilitate synaptic plasticity and modify neuronal function within prefrontal and hippocampal circuits. However, most studies have demonstrated these effects in animal models and translational studies in humans are scarce. A recent animal study showe...

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Main Authors: Anna Höflich, Christoph Kraus, Ruth M. Pfeiffer, Rene Seiger, Dan Rujescu, Carlos A. Zarate, Siegfried Kasper, Dietmar Winkler, Rupert Lanzenberger
Format: Article
Language:English
Published: Nature Publishing Group 2021-04-01
Series:Translational Psychiatry
Online Access:https://doi.org/10.1038/s41398-021-01318-6
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spelling doaj-dc4807d813a3499da37db0e0de1370992021-04-04T11:44:13ZengNature Publishing GroupTranslational Psychiatry2158-31882021-04-011111910.1038/s41398-021-01318-6Translating the immediate effects of S-Ketamine using hippocampal subfield analysis in healthy subjects-results of a randomized controlled trialAnna Höflich0Christoph Kraus1Ruth M. Pfeiffer2Rene Seiger3Dan Rujescu4Carlos A. Zarate5Siegfried Kasper6Dietmar Winkler7Rupert Lanzenberger8Department of Psychiatry and Psychotherapy, Medical University of ViennaDepartment of Psychiatry and Psychotherapy, Medical University of ViennaBiostatistics Branch, National Cancer Institute, National Institutes of HealthDepartment of Psychiatry and Psychotherapy, Medical University of ViennaDepartment of Psychiatry, Psychotherapy and Psychosomatics, Martin-Luther-University Halle-WittenbergExperimental Therapeutics and Pathophysiology Branch, National Institute of Mental Health, National Institutes of HealthDepartment of Psychiatry and Psychotherapy, Medical University of ViennaDepartment of Psychiatry and Psychotherapy, Medical University of ViennaDepartment of Psychiatry and Psychotherapy, Medical University of ViennaAbstract Antidepressant doses of ketamine rapidly facilitate synaptic plasticity and modify neuronal function within prefrontal and hippocampal circuits. However, most studies have demonstrated these effects in animal models and translational studies in humans are scarce. A recent animal study showed that ketamine restored dendritic spines in the hippocampal CA1 region within 1 h of administration. To translate these results to humans, this randomized, double-blind, placebo-controlled, crossover magnetic resonance imaging (MRI) study assessed ketamine’s rapid neuroplastic effects on hippocampal subfield measurements in healthy volunteers. S-Ketamine vs. placebo data were analyzed, and data were also grouped by brain-derived neurotrophic factor (BDNF) genotype. Linear mixed models showed that overall hippocampal subfield volumes were significantly larger (p = 0.009) post ketamine than post placebo (LS means difference=0.008, standard error=0.003). Post-hoc tests did not attribute effects to specific subfields (all p > 0.05). Trend-wise volumetric increases were observed within the left hippocampal CA1 region (p = 0.076), and trend-wise volumetric reductions were obtained in the right hippocampal—amygdaloid transition region (HATA) (p = 0.067). Neither genotype nor a genotype–drug interaction significantly affected the results (all p > 0.7). The study provides evidence that ketamine has short-term effects on hippocampal subfield volumes in humans. The results translate previous findings from animal models of depression showing that ketamine has pro-neuroplastic effects on hippocampal structures and underscore the importance of the hippocampus as a key region in ketamine’s mechanism of action.https://doi.org/10.1038/s41398-021-01318-6
collection DOAJ
language English
format Article
sources DOAJ
author Anna Höflich
Christoph Kraus
Ruth M. Pfeiffer
Rene Seiger
Dan Rujescu
Carlos A. Zarate
Siegfried Kasper
Dietmar Winkler
Rupert Lanzenberger
spellingShingle Anna Höflich
Christoph Kraus
Ruth M. Pfeiffer
Rene Seiger
Dan Rujescu
Carlos A. Zarate
Siegfried Kasper
Dietmar Winkler
Rupert Lanzenberger
Translating the immediate effects of S-Ketamine using hippocampal subfield analysis in healthy subjects-results of a randomized controlled trial
Translational Psychiatry
author_facet Anna Höflich
Christoph Kraus
Ruth M. Pfeiffer
Rene Seiger
Dan Rujescu
Carlos A. Zarate
Siegfried Kasper
Dietmar Winkler
Rupert Lanzenberger
author_sort Anna Höflich
title Translating the immediate effects of S-Ketamine using hippocampal subfield analysis in healthy subjects-results of a randomized controlled trial
title_short Translating the immediate effects of S-Ketamine using hippocampal subfield analysis in healthy subjects-results of a randomized controlled trial
title_full Translating the immediate effects of S-Ketamine using hippocampal subfield analysis in healthy subjects-results of a randomized controlled trial
title_fullStr Translating the immediate effects of S-Ketamine using hippocampal subfield analysis in healthy subjects-results of a randomized controlled trial
title_full_unstemmed Translating the immediate effects of S-Ketamine using hippocampal subfield analysis in healthy subjects-results of a randomized controlled trial
title_sort translating the immediate effects of s-ketamine using hippocampal subfield analysis in healthy subjects-results of a randomized controlled trial
publisher Nature Publishing Group
series Translational Psychiatry
issn 2158-3188
publishDate 2021-04-01
description Abstract Antidepressant doses of ketamine rapidly facilitate synaptic plasticity and modify neuronal function within prefrontal and hippocampal circuits. However, most studies have demonstrated these effects in animal models and translational studies in humans are scarce. A recent animal study showed that ketamine restored dendritic spines in the hippocampal CA1 region within 1 h of administration. To translate these results to humans, this randomized, double-blind, placebo-controlled, crossover magnetic resonance imaging (MRI) study assessed ketamine’s rapid neuroplastic effects on hippocampal subfield measurements in healthy volunteers. S-Ketamine vs. placebo data were analyzed, and data were also grouped by brain-derived neurotrophic factor (BDNF) genotype. Linear mixed models showed that overall hippocampal subfield volumes were significantly larger (p = 0.009) post ketamine than post placebo (LS means difference=0.008, standard error=0.003). Post-hoc tests did not attribute effects to specific subfields (all p > 0.05). Trend-wise volumetric increases were observed within the left hippocampal CA1 region (p = 0.076), and trend-wise volumetric reductions were obtained in the right hippocampal—amygdaloid transition region (HATA) (p = 0.067). Neither genotype nor a genotype–drug interaction significantly affected the results (all p > 0.7). The study provides evidence that ketamine has short-term effects on hippocampal subfield volumes in humans. The results translate previous findings from animal models of depression showing that ketamine has pro-neuroplastic effects on hippocampal structures and underscore the importance of the hippocampus as a key region in ketamine’s mechanism of action.
url https://doi.org/10.1038/s41398-021-01318-6
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