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Single and simultaneous effects of acrylamide and ethanol on bone microstructure of mice after one remodeling cycle
BACKGROUND: This study aimed to examine femoral bone microstructure of mice after single and simultaneous administration to acrylamide and ethanol since both substances are often consumed separately and/or together by humans. Interactive effects of these toxins were analysed after one remodeling cyc...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6604442/ https://www.ncbi.nlm.nih.gov/pubmed/31262364 http://dx.doi.org/10.1186/s40360-019-0317-7 |
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author | Sarocka, Anna Kovacova, Veronika Omelka, Radoslav Grosskopf, Birgit Kapusta, Edyta Goc, Zofia Formicki, Grzegorz Martiniakova, Monika |
author_facet | Sarocka, Anna Kovacova, Veronika Omelka, Radoslav Grosskopf, Birgit Kapusta, Edyta Goc, Zofia Formicki, Grzegorz Martiniakova, Monika |
author_sort | Sarocka, Anna |
collection | PubMed |
description | BACKGROUND: This study aimed to examine femoral bone microstructure of mice after single and simultaneous administration to acrylamide and ethanol since both substances are often consumed separately and/or together by humans. Interactive effects of these toxins were analysed after one remodeling cycle. METHODS: Twenty clinically healthy adult mice were randomly divided into four groups following 2 weeks administration of toxins: A group - mice were fed with acrylamide (40 mg/kg bw); E group - mice were ethanol-fed (15% ethanol); AE group - mice were simultaneously fed with both toxins, and a C group – control (without acrylamide and/or ethanol supplementation). Generally, 2D and 3D imaging methods were used to determine cortical and trabecular bone tissues microstructure. Biochemical analyses of plasma parameters were also realized using commercially available ELISA tests and spectrophotometrically. RESULTS: Single and simultaneous exposure to acrylamide and ethanol affected only cortical bone microstructure. No significant changes in trabecular bone morphometry were detected among all groups. In mice from the A group, increased endocortical remodeling associated with a higher level of serum calcium and vasoconstriction of primary osteon’s vascular canals (POVC) were identified. On the contrary, increased cortical porosity consistent with a decreased relative bone volume, bone mineral density (BMD) and lower levels of alkaline phosphatase (ALP), glutathione (GSH), calcium in plasma and also with vasodilation of POVC were observed in the E group. In the AE group, the highest density of secondary osteons associated with a lower BMD and decreased levels of ALP, GSH were documented. The parameters of POVC and Haversian canals approximated to the C group. In addition, single and simultaneous exposure to both toxins caused liver disease consistent with a higher values of alanine aminotransferase (ALT), aspartate aminotransferase (AST) in plasma of all experimental groups. CONCLUSIONS: Single administration to acrylamide and ethanol had negative effects on cortical bone structure of mice after one remodeling cycle. However, we identified possible antagonistic impact of these toxins on the structure of the cortical bone. |
format | Online Article Text |
id | pubmed-6604442 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-66044422019-07-12 Single and simultaneous effects of acrylamide and ethanol on bone microstructure of mice after one remodeling cycle Sarocka, Anna Kovacova, Veronika Omelka, Radoslav Grosskopf, Birgit Kapusta, Edyta Goc, Zofia Formicki, Grzegorz Martiniakova, Monika BMC Pharmacol Toxicol Research Article BACKGROUND: This study aimed to examine femoral bone microstructure of mice after single and simultaneous administration to acrylamide and ethanol since both substances are often consumed separately and/or together by humans. Interactive effects of these toxins were analysed after one remodeling cycle. METHODS: Twenty clinically healthy adult mice were randomly divided into four groups following 2 weeks administration of toxins: A group - mice were fed with acrylamide (40 mg/kg bw); E group - mice were ethanol-fed (15% ethanol); AE group - mice were simultaneously fed with both toxins, and a C group – control (without acrylamide and/or ethanol supplementation). Generally, 2D and 3D imaging methods were used to determine cortical and trabecular bone tissues microstructure. Biochemical analyses of plasma parameters were also realized using commercially available ELISA tests and spectrophotometrically. RESULTS: Single and simultaneous exposure to acrylamide and ethanol affected only cortical bone microstructure. No significant changes in trabecular bone morphometry were detected among all groups. In mice from the A group, increased endocortical remodeling associated with a higher level of serum calcium and vasoconstriction of primary osteon’s vascular canals (POVC) were identified. On the contrary, increased cortical porosity consistent with a decreased relative bone volume, bone mineral density (BMD) and lower levels of alkaline phosphatase (ALP), glutathione (GSH), calcium in plasma and also with vasodilation of POVC were observed in the E group. In the AE group, the highest density of secondary osteons associated with a lower BMD and decreased levels of ALP, GSH were documented. The parameters of POVC and Haversian canals approximated to the C group. In addition, single and simultaneous exposure to both toxins caused liver disease consistent with a higher values of alanine aminotransferase (ALT), aspartate aminotransferase (AST) in plasma of all experimental groups. CONCLUSIONS: Single administration to acrylamide and ethanol had negative effects on cortical bone structure of mice after one remodeling cycle. However, we identified possible antagonistic impact of these toxins on the structure of the cortical bone. BioMed Central 2019-07-01 /pmc/articles/PMC6604442/ /pubmed/31262364 http://dx.doi.org/10.1186/s40360-019-0317-7 Text en © The Author(s). 2019 Open AccessThis 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. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Sarocka, Anna Kovacova, Veronika Omelka, Radoslav Grosskopf, Birgit Kapusta, Edyta Goc, Zofia Formicki, Grzegorz Martiniakova, Monika Single and simultaneous effects of acrylamide and ethanol on bone microstructure of mice after one remodeling cycle |
title | Single and simultaneous effects of acrylamide and ethanol on bone microstructure of mice after one remodeling cycle |
title_full | Single and simultaneous effects of acrylamide and ethanol on bone microstructure of mice after one remodeling cycle |
title_fullStr | Single and simultaneous effects of acrylamide and ethanol on bone microstructure of mice after one remodeling cycle |
title_full_unstemmed | Single and simultaneous effects of acrylamide and ethanol on bone microstructure of mice after one remodeling cycle |
title_short | Single and simultaneous effects of acrylamide and ethanol on bone microstructure of mice after one remodeling cycle |
title_sort | single and simultaneous effects of acrylamide and ethanol on bone microstructure of mice after one remodeling cycle |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6604442/ https://www.ncbi.nlm.nih.gov/pubmed/31262364 http://dx.doi.org/10.1186/s40360-019-0317-7 |
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