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Functional ultrasound detects frequency-specific acute and delayed S-ketamine effects in the healthy mouse brain

INTRODUCTION: S-ketamine has received great interest due to both its antidepressant effects and its potential to induce psychosis when administered subchronically. However, no studies have investigated both its acute and delayed effects using in vivo small-animal imaging. Recently, functional ultras...

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Autores principales: Ionescu, Tudor M., Grohs-Metz, Gillian, Hengerer, Bastian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10229773/
https://www.ncbi.nlm.nih.gov/pubmed/37266546
http://dx.doi.org/10.3389/fnins.2023.1177428
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author Ionescu, Tudor M.
Grohs-Metz, Gillian
Hengerer, Bastian
author_facet Ionescu, Tudor M.
Grohs-Metz, Gillian
Hengerer, Bastian
author_sort Ionescu, Tudor M.
collection PubMed
description INTRODUCTION: S-ketamine has received great interest due to both its antidepressant effects and its potential to induce psychosis when administered subchronically. However, no studies have investigated both its acute and delayed effects using in vivo small-animal imaging. Recently, functional ultrasound (fUS) has emerged as a powerful alternative to functional magnetic resonance imaging (fMRI), outperforming it in sensitivity and in spatiotemporal resolution. In this study, we employed fUS to thoroughly characterize acute and delayed S-ketamine effects on functional connectivity (FC) within the same cohort at slow frequency bands ranging from 0.01 to 1.25 Hz, previously reported to exhibit FC. METHODS: We acquired fUS in a total of 16 healthy C57/Bl6 mice split in two cohorts (n = 8 received saline, n = 8 S-ketamine). One day after the first scans, performed at rest, the mice received the first dose of S-ketamine during the second measurement, followed by four further doses administered every 2 days. First, we assessed FC reproducibility and reliability at baseline in six frequency bands. Then, we investigated the acute and delayed effects at day 1 after the first dose and at day 9, 1 day after the last dose, for all bands, resulting in a total of four fUS measurements for every mouse. RESULTS: We found reproducible (r > 0.9) and reliable (r > 0.9) group-average readouts in all frequency bands, only the 0.01–0.27 Hz band performing slightly worse. Acutely, S-ketamine induced strong FC increases in five of the six bands, peaking in the 0.073–0.2 Hz band. These increases comprised both cortical and subcortical brain areas, yet were of a transient nature, FC almost returning to baseline levels towards the end of the scan. Intriguingly, we observed robust corticostriatal FC decreases in the fastest band acquired (0.75 Hz–1.25  Hz). These changes persisted to a weaker extent after 1 day and at this timepoint they were accompanied by decreases in the other five bands as well. After 9 days, the decreases in the 0.75–1.25 Hz band were maintained, however no changes between cohorts could be detected in any other bands. DISCUSSION: In summary, the study reports that acute and delayed ketamine effects in mice are not only dissimilar but have different directionalities in most frequency bands. The complementary readouts of the employed frequency bands recommend the use of fUS for frequency-specific investigation of pharmacological effects on FC.
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spelling pubmed-102297732023-06-01 Functional ultrasound detects frequency-specific acute and delayed S-ketamine effects in the healthy mouse brain Ionescu, Tudor M. Grohs-Metz, Gillian Hengerer, Bastian Front Neurosci Neuroscience INTRODUCTION: S-ketamine has received great interest due to both its antidepressant effects and its potential to induce psychosis when administered subchronically. However, no studies have investigated both its acute and delayed effects using in vivo small-animal imaging. Recently, functional ultrasound (fUS) has emerged as a powerful alternative to functional magnetic resonance imaging (fMRI), outperforming it in sensitivity and in spatiotemporal resolution. In this study, we employed fUS to thoroughly characterize acute and delayed S-ketamine effects on functional connectivity (FC) within the same cohort at slow frequency bands ranging from 0.01 to 1.25 Hz, previously reported to exhibit FC. METHODS: We acquired fUS in a total of 16 healthy C57/Bl6 mice split in two cohorts (n = 8 received saline, n = 8 S-ketamine). One day after the first scans, performed at rest, the mice received the first dose of S-ketamine during the second measurement, followed by four further doses administered every 2 days. First, we assessed FC reproducibility and reliability at baseline in six frequency bands. Then, we investigated the acute and delayed effects at day 1 after the first dose and at day 9, 1 day after the last dose, for all bands, resulting in a total of four fUS measurements for every mouse. RESULTS: We found reproducible (r > 0.9) and reliable (r > 0.9) group-average readouts in all frequency bands, only the 0.01–0.27 Hz band performing slightly worse. Acutely, S-ketamine induced strong FC increases in five of the six bands, peaking in the 0.073–0.2 Hz band. These increases comprised both cortical and subcortical brain areas, yet were of a transient nature, FC almost returning to baseline levels towards the end of the scan. Intriguingly, we observed robust corticostriatal FC decreases in the fastest band acquired (0.75 Hz–1.25  Hz). These changes persisted to a weaker extent after 1 day and at this timepoint they were accompanied by decreases in the other five bands as well. After 9 days, the decreases in the 0.75–1.25 Hz band were maintained, however no changes between cohorts could be detected in any other bands. DISCUSSION: In summary, the study reports that acute and delayed ketamine effects in mice are not only dissimilar but have different directionalities in most frequency bands. The complementary readouts of the employed frequency bands recommend the use of fUS for frequency-specific investigation of pharmacological effects on FC. Frontiers Media S.A. 2023-05-17 /pmc/articles/PMC10229773/ /pubmed/37266546 http://dx.doi.org/10.3389/fnins.2023.1177428 Text en Copyright © 2023 Ionescu, Grohs-Metz and Hengerer. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Ionescu, Tudor M.
Grohs-Metz, Gillian
Hengerer, Bastian
Functional ultrasound detects frequency-specific acute and delayed S-ketamine effects in the healthy mouse brain
title Functional ultrasound detects frequency-specific acute and delayed S-ketamine effects in the healthy mouse brain
title_full Functional ultrasound detects frequency-specific acute and delayed S-ketamine effects in the healthy mouse brain
title_fullStr Functional ultrasound detects frequency-specific acute and delayed S-ketamine effects in the healthy mouse brain
title_full_unstemmed Functional ultrasound detects frequency-specific acute and delayed S-ketamine effects in the healthy mouse brain
title_short Functional ultrasound detects frequency-specific acute and delayed S-ketamine effects in the healthy mouse brain
title_sort functional ultrasound detects frequency-specific acute and delayed s-ketamine effects in the healthy mouse brain
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10229773/
https://www.ncbi.nlm.nih.gov/pubmed/37266546
http://dx.doi.org/10.3389/fnins.2023.1177428
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