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The effect of a single dose of escitalopram on sensorimotor networks
INTRODUCTION: Serving as a pilot study of poststroke pharmacotherapy, the present investigation was intended to establish the effect of a single dose of escitalopram on motor task performance in normal volunteers. METHODS: Ten healthy volunteers of median age 63 years including four females performe...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5991571/ https://www.ncbi.nlm.nih.gov/pubmed/30106253 http://dx.doi.org/10.1002/brb3.975 |
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author | Weisstanner, Christian Kägi, Georg Krammer, Werner Eap, Chin B. Wiest, Roland Missimer, John H. Weder, Bruno J. |
author_facet | Weisstanner, Christian Kägi, Georg Krammer, Werner Eap, Chin B. Wiest, Roland Missimer, John H. Weder, Bruno J. |
author_sort | Weisstanner, Christian |
collection | PubMed |
description | INTRODUCTION: Serving as a pilot study of poststroke pharmacotherapy, the present investigation was intended to establish the effect of a single dose of escitalopram on motor task performance in normal volunteers. METHODS: Ten healthy volunteers of median age 63 years including four females performed a well‐studied tactile manipulation task in two fMRI sessions using a double‐blind cross‐over design. The sessions began approximately three hours after ingestion of 20 mg escitalopram or placebo presented in pseudorandom order. The fMRI image sequences were submitted to principal component analysis (PCA). RESULTS: Based on volume correlations of task‐related principal components with the mean component images derived in our previous study, we established the reproducibility of two networks of sensorimotor activity proposed there. The network reflecting motor control (cerebral pattern I) appeared invariably in placebo and verum conditions. In contrast, the other network, attributed to diminished motor control due to distracting mental processing (cerebral pattern II), emerged less regularly and exhibited more variability. Second‐level PCAs of both conditions confirmed the findings of the initial analysis. Specifically, it validated the dominant and invariable expression of cerebral pattern I after application of a single dose of escitalopram. Dynamic causal modeling confirmed enhanced motor output as a result of a significantly increased connectivity between primary motor cortex and dorsal premotor cortex. CONCLUSION: This pilot study suggests the promise of stimulation by a specific serotonin reuptake inhibitor in regard to recovery and preservation of motor control after stroke. |
format | Online Article Text |
id | pubmed-5991571 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-59915712018-06-20 The effect of a single dose of escitalopram on sensorimotor networks Weisstanner, Christian Kägi, Georg Krammer, Werner Eap, Chin B. Wiest, Roland Missimer, John H. Weder, Bruno J. Brain Behav Original Research INTRODUCTION: Serving as a pilot study of poststroke pharmacotherapy, the present investigation was intended to establish the effect of a single dose of escitalopram on motor task performance in normal volunteers. METHODS: Ten healthy volunteers of median age 63 years including four females performed a well‐studied tactile manipulation task in two fMRI sessions using a double‐blind cross‐over design. The sessions began approximately three hours after ingestion of 20 mg escitalopram or placebo presented in pseudorandom order. The fMRI image sequences were submitted to principal component analysis (PCA). RESULTS: Based on volume correlations of task‐related principal components with the mean component images derived in our previous study, we established the reproducibility of two networks of sensorimotor activity proposed there. The network reflecting motor control (cerebral pattern I) appeared invariably in placebo and verum conditions. In contrast, the other network, attributed to diminished motor control due to distracting mental processing (cerebral pattern II), emerged less regularly and exhibited more variability. Second‐level PCAs of both conditions confirmed the findings of the initial analysis. Specifically, it validated the dominant and invariable expression of cerebral pattern I after application of a single dose of escitalopram. Dynamic causal modeling confirmed enhanced motor output as a result of a significantly increased connectivity between primary motor cortex and dorsal premotor cortex. CONCLUSION: This pilot study suggests the promise of stimulation by a specific serotonin reuptake inhibitor in regard to recovery and preservation of motor control after stroke. John Wiley and Sons Inc. 2018-04-20 /pmc/articles/PMC5991571/ /pubmed/30106253 http://dx.doi.org/10.1002/brb3.975 Text en © 2018 The Authors. Brain and Behavior published by Wiley Periodicals, Inc. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Research Weisstanner, Christian Kägi, Georg Krammer, Werner Eap, Chin B. Wiest, Roland Missimer, John H. Weder, Bruno J. The effect of a single dose of escitalopram on sensorimotor networks |
title | The effect of a single dose of escitalopram on sensorimotor networks |
title_full | The effect of a single dose of escitalopram on sensorimotor networks |
title_fullStr | The effect of a single dose of escitalopram on sensorimotor networks |
title_full_unstemmed | The effect of a single dose of escitalopram on sensorimotor networks |
title_short | The effect of a single dose of escitalopram on sensorimotor networks |
title_sort | effect of a single dose of escitalopram on sensorimotor networks |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5991571/ https://www.ncbi.nlm.nih.gov/pubmed/30106253 http://dx.doi.org/10.1002/brb3.975 |
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