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Deciphering the scopolamine challenge rat model by preclinical functional MRI

During preclinical drug testing, the systemic administration of scopolamine (SCO), a cholinergic antagonist, is widely used. However, it suffers important limitations, like non-specific behavioural effects partly due to its peripheral side-effects. Therefore, neuroimaging measures would enhance its...

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Autores principales: Somogyi, Gergely, Hlatky, Dávid, Spisák, Tamás, Spisák, Zsófia, Nyitrai, Gabriella, Czurkó, András
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8149883/
https://www.ncbi.nlm.nih.gov/pubmed/34035328
http://dx.doi.org/10.1038/s41598-021-90273-9
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author Somogyi, Gergely
Hlatky, Dávid
Spisák, Tamás
Spisák, Zsófia
Nyitrai, Gabriella
Czurkó, András
author_facet Somogyi, Gergely
Hlatky, Dávid
Spisák, Tamás
Spisák, Zsófia
Nyitrai, Gabriella
Czurkó, András
author_sort Somogyi, Gergely
collection PubMed
description During preclinical drug testing, the systemic administration of scopolamine (SCO), a cholinergic antagonist, is widely used. However, it suffers important limitations, like non-specific behavioural effects partly due to its peripheral side-effects. Therefore, neuroimaging measures would enhance its translational value. To this end, in Wistar rats, we measured whisker-stimulation induced functional MRI activation after SCO, peripherally acting butylscopolamine (BSCO), or saline administration in a cross-over design. Besides the commonly used gradient-echo echo-planar imaging (GE EPI), we also used an arterial spin labeling method in isoflurane anesthesia. With the GE EPI measurement, SCO decreased the evoked BOLD response in the barrel cortex (BC), while BSCO increased it in the anterior cingulate cortex. In a second experiment, we used GE EPI and spin-echo (SE) EPI sequences in a combined (isoflurane + i.p. dexmedetomidine) anesthesia to account for anesthesia-effects. Here, we also examined the effect of donepezil. In the combined anesthesia, with the GE EPI, SCO decreased the activation in the BC and the inferior colliculus (IC). BSCO reduced the response merely in the IC. Our results revealed that SCO attenuated the evoked BOLD activation in the BC as a probable central effect in both experiments. The likely peripheral vascular actions of SCO with the given fMRI sequences depended on the type of anesthesia or its dose.
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spelling pubmed-81498832021-05-26 Deciphering the scopolamine challenge rat model by preclinical functional MRI Somogyi, Gergely Hlatky, Dávid Spisák, Tamás Spisák, Zsófia Nyitrai, Gabriella Czurkó, András Sci Rep Article During preclinical drug testing, the systemic administration of scopolamine (SCO), a cholinergic antagonist, is widely used. However, it suffers important limitations, like non-specific behavioural effects partly due to its peripheral side-effects. Therefore, neuroimaging measures would enhance its translational value. To this end, in Wistar rats, we measured whisker-stimulation induced functional MRI activation after SCO, peripherally acting butylscopolamine (BSCO), or saline administration in a cross-over design. Besides the commonly used gradient-echo echo-planar imaging (GE EPI), we also used an arterial spin labeling method in isoflurane anesthesia. With the GE EPI measurement, SCO decreased the evoked BOLD response in the barrel cortex (BC), while BSCO increased it in the anterior cingulate cortex. In a second experiment, we used GE EPI and spin-echo (SE) EPI sequences in a combined (isoflurane + i.p. dexmedetomidine) anesthesia to account for anesthesia-effects. Here, we also examined the effect of donepezil. In the combined anesthesia, with the GE EPI, SCO decreased the activation in the BC and the inferior colliculus (IC). BSCO reduced the response merely in the IC. Our results revealed that SCO attenuated the evoked BOLD activation in the BC as a probable central effect in both experiments. The likely peripheral vascular actions of SCO with the given fMRI sequences depended on the type of anesthesia or its dose. Nature Publishing Group UK 2021-05-25 /pmc/articles/PMC8149883/ /pubmed/34035328 http://dx.doi.org/10.1038/s41598-021-90273-9 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Somogyi, Gergely
Hlatky, Dávid
Spisák, Tamás
Spisák, Zsófia
Nyitrai, Gabriella
Czurkó, András
Deciphering the scopolamine challenge rat model by preclinical functional MRI
title Deciphering the scopolamine challenge rat model by preclinical functional MRI
title_full Deciphering the scopolamine challenge rat model by preclinical functional MRI
title_fullStr Deciphering the scopolamine challenge rat model by preclinical functional MRI
title_full_unstemmed Deciphering the scopolamine challenge rat model by preclinical functional MRI
title_short Deciphering the scopolamine challenge rat model by preclinical functional MRI
title_sort deciphering the scopolamine challenge rat model by preclinical functional mri
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8149883/
https://www.ncbi.nlm.nih.gov/pubmed/34035328
http://dx.doi.org/10.1038/s41598-021-90273-9
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