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Assessment of cellular and molecular changes in the rat brain after gamma radiation and radioprotection by anisomycin
The objective of the study was to describe cellular and molecular markers of radioprotection by anisomycin, focusing on the changes in rat brain tissue. Two-month-old Wistar rats were exposed to a (60)Co radiation source at a dose of 6 Gy, with or without radioprotection with anisomycin (150 mg/kg)...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Oxford University Press
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8438266/ https://www.ncbi.nlm.nih.gov/pubmed/34062561 http://dx.doi.org/10.1093/jrr/rrab045 |
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author | Kočović, Dušica M Bajuk-Bogdanović, Danica Pećinar, Ilinka Nedeljković, Biljana Božić Daković, Marko Andjus, Pavle R |
author_facet | Kočović, Dušica M Bajuk-Bogdanović, Danica Pećinar, Ilinka Nedeljković, Biljana Božić Daković, Marko Andjus, Pavle R |
author_sort | Kočović, Dušica M |
collection | PubMed |
description | The objective of the study was to describe cellular and molecular markers of radioprotection by anisomycin, focusing on the changes in rat brain tissue. Two-month-old Wistar rats were exposed to a (60)Co radiation source at a dose of 6 Gy, with or without radioprotection with anisomycin (150 mg/kg) administered subcutaneously 30 min before or 3 or 6 h after irradiation. Survivors were analyzed 30 days after treatment. Astroglial and microglial responses were investigated based on the expression of glial markers assessed with immunohistochemistry, and quantitative changes in brain biomolecules were investigated by Raman microspectroscopy. In addition, blood plasma levels of pro-inflammatory (interleukin 6 and tumor necrosis factor α) and anti-inflammatory (interleukin 10) cytokines were assessed. We found that application of anisomycin either before or after irradiation significantly decreased the expression of the microglial marker Iba-1. We also found an increased intensity of Raman spectral bands related to nucleic acids, as well as an increased level of cytokines when anisomycin was applied after irradiation. This suggests that the radioprotective effects of anisomycin are by decreasing Iba-1 expression and stabilizing genetic material by increasing the level of nucleic acids. |
format | Online Article Text |
id | pubmed-8438266 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-84382662021-09-15 Assessment of cellular and molecular changes in the rat brain after gamma radiation and radioprotection by anisomycin Kočović, Dušica M Bajuk-Bogdanović, Danica Pećinar, Ilinka Nedeljković, Biljana Božić Daković, Marko Andjus, Pavle R J Radiat Res Fundamental Radiation Science The objective of the study was to describe cellular and molecular markers of radioprotection by anisomycin, focusing on the changes in rat brain tissue. Two-month-old Wistar rats were exposed to a (60)Co radiation source at a dose of 6 Gy, with or without radioprotection with anisomycin (150 mg/kg) administered subcutaneously 30 min before or 3 or 6 h after irradiation. Survivors were analyzed 30 days after treatment. Astroglial and microglial responses were investigated based on the expression of glial markers assessed with immunohistochemistry, and quantitative changes in brain biomolecules were investigated by Raman microspectroscopy. In addition, blood plasma levels of pro-inflammatory (interleukin 6 and tumor necrosis factor α) and anti-inflammatory (interleukin 10) cytokines were assessed. We found that application of anisomycin either before or after irradiation significantly decreased the expression of the microglial marker Iba-1. We also found an increased intensity of Raman spectral bands related to nucleic acids, as well as an increased level of cytokines when anisomycin was applied after irradiation. This suggests that the radioprotective effects of anisomycin are by decreasing Iba-1 expression and stabilizing genetic material by increasing the level of nucleic acids. Oxford University Press 2021-06-01 /pmc/articles/PMC8438266/ /pubmed/34062561 http://dx.doi.org/10.1093/jrr/rrab045 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of The Japanese Radiation Research Society and Japanese Society for Radiation Oncology. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Fundamental Radiation Science Kočović, Dušica M Bajuk-Bogdanović, Danica Pećinar, Ilinka Nedeljković, Biljana Božić Daković, Marko Andjus, Pavle R Assessment of cellular and molecular changes in the rat brain after gamma radiation and radioprotection by anisomycin |
title | Assessment of cellular and molecular changes in the rat brain after gamma radiation and radioprotection by anisomycin |
title_full | Assessment of cellular and molecular changes in the rat brain after gamma radiation and radioprotection by anisomycin |
title_fullStr | Assessment of cellular and molecular changes in the rat brain after gamma radiation and radioprotection by anisomycin |
title_full_unstemmed | Assessment of cellular and molecular changes in the rat brain after gamma radiation and radioprotection by anisomycin |
title_short | Assessment of cellular and molecular changes in the rat brain after gamma radiation and radioprotection by anisomycin |
title_sort | assessment of cellular and molecular changes in the rat brain after gamma radiation and radioprotection by anisomycin |
topic | Fundamental Radiation Science |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8438266/ https://www.ncbi.nlm.nih.gov/pubmed/34062561 http://dx.doi.org/10.1093/jrr/rrab045 |
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