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Neurobehavioral effects of uremic toxin–indoxyl sulfate in the rat model

Chronic kidney disease (CKD) is deemed to be a worldwide health concern connected with neurological manifestations. The etiology of central nervous system (CNS) disorders in CKD is still not fully understood, however particular attention is currently being paid to the impact of accumulated toxins. I...

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Autores principales: Karbowska, Malgorzata, Hermanowicz, Justyna M., Tankiewicz-Kwedlo, Anna, Kalaska, Bartlomiej, Kaminski, Tomasz W., Nosek, Krzysztof, Wisniewska, Roza J., Pawlak, Dariusz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7289875/
https://www.ncbi.nlm.nih.gov/pubmed/32528183
http://dx.doi.org/10.1038/s41598-020-66421-y
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author Karbowska, Malgorzata
Hermanowicz, Justyna M.
Tankiewicz-Kwedlo, Anna
Kalaska, Bartlomiej
Kaminski, Tomasz W.
Nosek, Krzysztof
Wisniewska, Roza J.
Pawlak, Dariusz
author_facet Karbowska, Malgorzata
Hermanowicz, Justyna M.
Tankiewicz-Kwedlo, Anna
Kalaska, Bartlomiej
Kaminski, Tomasz W.
Nosek, Krzysztof
Wisniewska, Roza J.
Pawlak, Dariusz
author_sort Karbowska, Malgorzata
collection PubMed
description Chronic kidney disease (CKD) is deemed to be a worldwide health concern connected with neurological manifestations. The etiology of central nervous system (CNS) disorders in CKD is still not fully understood, however particular attention is currently being paid to the impact of accumulated toxins. Indoxyl sulfate (IS) is one of the most potent uremic toxins. The purpose of the present study was to assess IS concentrations in the cerebellum, brainstem, cortex, hypothalamus, and striatum with hippocampus of rats chronically exposed to IS. To evaluate IS impact on neurochemical and behavioral alterations, we examined its influence on brain levels of norepinephrine, epinephrine, dopamine, serotonin and their metabolites, as well as changes in behavioral tests (open field test, elevated plus maze test, chimney test, T maze test, and splash test). Our results show the highest IS accumulation in the brainstem. IS leads to behavioral alterations involving apathetic behavior, increased stress sensitivity, and reduced locomotor and exploratory activity. Besides, IS contributes to the impairment of spatial memory and motor coordination. Furthermore, we observed reduced levels of norepinephrine, dopamine or serotonin, mainly in the brainstem. Our findings indicate that IS can be one of the crucial uremic factors responsible for altered mental status in CKD.
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spelling pubmed-72898752020-06-15 Neurobehavioral effects of uremic toxin–indoxyl sulfate in the rat model Karbowska, Malgorzata Hermanowicz, Justyna M. Tankiewicz-Kwedlo, Anna Kalaska, Bartlomiej Kaminski, Tomasz W. Nosek, Krzysztof Wisniewska, Roza J. Pawlak, Dariusz Sci Rep Article Chronic kidney disease (CKD) is deemed to be a worldwide health concern connected with neurological manifestations. The etiology of central nervous system (CNS) disorders in CKD is still not fully understood, however particular attention is currently being paid to the impact of accumulated toxins. Indoxyl sulfate (IS) is one of the most potent uremic toxins. The purpose of the present study was to assess IS concentrations in the cerebellum, brainstem, cortex, hypothalamus, and striatum with hippocampus of rats chronically exposed to IS. To evaluate IS impact on neurochemical and behavioral alterations, we examined its influence on brain levels of norepinephrine, epinephrine, dopamine, serotonin and their metabolites, as well as changes in behavioral tests (open field test, elevated plus maze test, chimney test, T maze test, and splash test). Our results show the highest IS accumulation in the brainstem. IS leads to behavioral alterations involving apathetic behavior, increased stress sensitivity, and reduced locomotor and exploratory activity. Besides, IS contributes to the impairment of spatial memory and motor coordination. Furthermore, we observed reduced levels of norepinephrine, dopamine or serotonin, mainly in the brainstem. Our findings indicate that IS can be one of the crucial uremic factors responsible for altered mental status in CKD. Nature Publishing Group UK 2020-06-11 /pmc/articles/PMC7289875/ /pubmed/32528183 http://dx.doi.org/10.1038/s41598-020-66421-y Text en © The Author(s) 2020 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Karbowska, Malgorzata
Hermanowicz, Justyna M.
Tankiewicz-Kwedlo, Anna
Kalaska, Bartlomiej
Kaminski, Tomasz W.
Nosek, Krzysztof
Wisniewska, Roza J.
Pawlak, Dariusz
Neurobehavioral effects of uremic toxin–indoxyl sulfate in the rat model
title Neurobehavioral effects of uremic toxin–indoxyl sulfate in the rat model
title_full Neurobehavioral effects of uremic toxin–indoxyl sulfate in the rat model
title_fullStr Neurobehavioral effects of uremic toxin–indoxyl sulfate in the rat model
title_full_unstemmed Neurobehavioral effects of uremic toxin–indoxyl sulfate in the rat model
title_short Neurobehavioral effects of uremic toxin–indoxyl sulfate in the rat model
title_sort neurobehavioral effects of uremic toxin–indoxyl sulfate in the rat model
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7289875/
https://www.ncbi.nlm.nih.gov/pubmed/32528183
http://dx.doi.org/10.1038/s41598-020-66421-y
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