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Fluoride Alteration of [(3)H]Glucose Uptake in Wistar Rat Brain and Peripheral Tissues

The present study was designed to investigate the role of postnatal fluoride intake on [3H]glucose uptake and transport in rat brain and peripheral tissues. Sodium fluoride (NaF) in a concentration of 10 or 50 ppm was added to the drinking water of adult Wistar rats. The control group received disti...

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Autores principales: Rogalska, Anna, Kuter, Katarzyna, Żelazko, Aleksandra, Głogowska-Gruszka, Anna, Świętochowska, Elżbieta, Nowak, Przemysław
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2017
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5360833/
https://www.ncbi.nlm.nih.gov/pubmed/28243943
http://dx.doi.org/10.1007/s12640-017-9709-x
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author Rogalska, Anna
Kuter, Katarzyna
Żelazko, Aleksandra
Głogowska-Gruszka, Anna
Świętochowska, Elżbieta
Nowak, Przemysław
author_facet Rogalska, Anna
Kuter, Katarzyna
Żelazko, Aleksandra
Głogowska-Gruszka, Anna
Świętochowska, Elżbieta
Nowak, Przemysław
author_sort Rogalska, Anna
collection PubMed
description The present study was designed to investigate the role of postnatal fluoride intake on [3H]glucose uptake and transport in rat brain and peripheral tissues. Sodium fluoride (NaF) in a concentration of 10 or 50 ppm was added to the drinking water of adult Wistar rats. The control group received distilled water. After 4 weeks, respective plasma fluoride levels were 0.0541 ± 0.0135 μg/ml (control), 0.0596 ± 0.0202 μg/ml (10 ppm), and 0.0823 ± 0.0199 μg/ml (50 ppm). Although plasma glucose levels were not altered in any group, the plasma insulin level in the fluoride (50 ppm) group was elevated (0.72 ± 0.13 μg/ml) versus the control group (0.48 ± 0.24 μg/ml) and fluoride (10 ppm) group. In rats receiving fluoride for 4 weeks at 10 ppm in drinking water, [3H]glucose uptake was unaltered in all tested parts of the brain. However, in rats receiving fluoride at 50 ppm, [3H]glucose uptake in cerebral cortex, hippocampus, and thalamus with hypothalamus was elevated, versus the saline group. Fluoride intake had a negligible effect on [3H]glucose uptake by peripheral tissues (liver, pancreas, stomach, small intestine, atrium, aorta, kidney, visceral tissue, lung, skin, oral mucosa, tongue, salivary gland, incisor, molars, and jawbone). In neither fluoride group was glucose transporter proteins 1 (GLUT 1) or 3 (GLUT 3) altered in frontal cortex and striatum versus control. On the assumption that increased glucose uptake (by neural tissue) reasonably reflects neuronal activity, it appears that fluoride damage to the brain results in a compensatory increase in glucose uptake and utilization without changes in GLUT 1 and GLUT 3 expression.
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spelling pubmed-53608332017-04-04 Fluoride Alteration of [(3)H]Glucose Uptake in Wistar Rat Brain and Peripheral Tissues Rogalska, Anna Kuter, Katarzyna Żelazko, Aleksandra Głogowska-Gruszka, Anna Świętochowska, Elżbieta Nowak, Przemysław Neurotox Res Original Article The present study was designed to investigate the role of postnatal fluoride intake on [3H]glucose uptake and transport in rat brain and peripheral tissues. Sodium fluoride (NaF) in a concentration of 10 or 50 ppm was added to the drinking water of adult Wistar rats. The control group received distilled water. After 4 weeks, respective plasma fluoride levels were 0.0541 ± 0.0135 μg/ml (control), 0.0596 ± 0.0202 μg/ml (10 ppm), and 0.0823 ± 0.0199 μg/ml (50 ppm). Although plasma glucose levels were not altered in any group, the plasma insulin level in the fluoride (50 ppm) group was elevated (0.72 ± 0.13 μg/ml) versus the control group (0.48 ± 0.24 μg/ml) and fluoride (10 ppm) group. In rats receiving fluoride for 4 weeks at 10 ppm in drinking water, [3H]glucose uptake was unaltered in all tested parts of the brain. However, in rats receiving fluoride at 50 ppm, [3H]glucose uptake in cerebral cortex, hippocampus, and thalamus with hypothalamus was elevated, versus the saline group. Fluoride intake had a negligible effect on [3H]glucose uptake by peripheral tissues (liver, pancreas, stomach, small intestine, atrium, aorta, kidney, visceral tissue, lung, skin, oral mucosa, tongue, salivary gland, incisor, molars, and jawbone). In neither fluoride group was glucose transporter proteins 1 (GLUT 1) or 3 (GLUT 3) altered in frontal cortex and striatum versus control. On the assumption that increased glucose uptake (by neural tissue) reasonably reflects neuronal activity, it appears that fluoride damage to the brain results in a compensatory increase in glucose uptake and utilization without changes in GLUT 1 and GLUT 3 expression. Springer US 2017-02-27 2017 /pmc/articles/PMC5360833/ /pubmed/28243943 http://dx.doi.org/10.1007/s12640-017-9709-x Text en © The Author(s) 2017 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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.
spellingShingle Original Article
Rogalska, Anna
Kuter, Katarzyna
Żelazko, Aleksandra
Głogowska-Gruszka, Anna
Świętochowska, Elżbieta
Nowak, Przemysław
Fluoride Alteration of [(3)H]Glucose Uptake in Wistar Rat Brain and Peripheral Tissues
title Fluoride Alteration of [(3)H]Glucose Uptake in Wistar Rat Brain and Peripheral Tissues
title_full Fluoride Alteration of [(3)H]Glucose Uptake in Wistar Rat Brain and Peripheral Tissues
title_fullStr Fluoride Alteration of [(3)H]Glucose Uptake in Wistar Rat Brain and Peripheral Tissues
title_full_unstemmed Fluoride Alteration of [(3)H]Glucose Uptake in Wistar Rat Brain and Peripheral Tissues
title_short Fluoride Alteration of [(3)H]Glucose Uptake in Wistar Rat Brain and Peripheral Tissues
title_sort fluoride alteration of [(3)h]glucose uptake in wistar rat brain and peripheral tissues
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5360833/
https://www.ncbi.nlm.nih.gov/pubmed/28243943
http://dx.doi.org/10.1007/s12640-017-9709-x
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