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Systemic administration of heparin ameliorates radiation-induced oral mucositis—preclinical studies in mice
PURPOSE: The present study investigates the impact of systemic application of heparins on the manifestation of radiation-induced oral mucositis in a well-established mouse model. MATERIALS AND METHODS: Male C3H/Neu mice were irradiated with either single-dose or fractionated irradiation protocols wi...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6008356/ https://www.ncbi.nlm.nih.gov/pubmed/29663036 http://dx.doi.org/10.1007/s00066-018-1300-8 |
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author | Kowaliuk, Maria Bozsaky, Eva Gruber, Sylvia Kuess, Peter Dörr, Wolfgang |
author_facet | Kowaliuk, Maria Bozsaky, Eva Gruber, Sylvia Kuess, Peter Dörr, Wolfgang |
author_sort | Kowaliuk, Maria |
collection | PubMed |
description | PURPOSE: The present study investigates the impact of systemic application of heparins on the manifestation of radiation-induced oral mucositis in a well-established mouse model. MATERIALS AND METHODS: Male C3H/Neu mice were irradiated with either single-dose or fractionated irradiation protocols with 5 × 3 Gy/week, given over one (days 0–4) or two (days 0–4, 7–11) weeks. All fractionation protocols were concluded by a local test irradiation (day 7/14) using graded doses to generate complete dose–effect curves. Daily doses of unfractionated or low molecular weight heparin (40 or 200 I.U./mouse, respectively) were applied subcutaneously over varying time intervals. The incidence and the time course of mucosal ulceration, corresponding to confluent mucositis in patients (RTOG/EORTC grade 3), were analysed as clinically relevant endpoints. RESULTS: Systemic application of heparins significantly increased the iso-effective doses for the induction of mucosal ulceration, particularly in combination with fractionated irradiation protocols. Moreover, a tentative prolongation of the latent time and a pronounced reduction of the ulcer duration were observed. CONCLUSION: These data provide the first evidence for a protective and/or mitigative effect of heparins for radiation-induced oral mucositis. Further studies are ongoing investigating the underlying mechanism. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00066-018-1300-8) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6008356 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-60083562018-07-04 Systemic administration of heparin ameliorates radiation-induced oral mucositis—preclinical studies in mice Kowaliuk, Maria Bozsaky, Eva Gruber, Sylvia Kuess, Peter Dörr, Wolfgang Strahlenther Onkol Original Article PURPOSE: The present study investigates the impact of systemic application of heparins on the manifestation of radiation-induced oral mucositis in a well-established mouse model. MATERIALS AND METHODS: Male C3H/Neu mice were irradiated with either single-dose or fractionated irradiation protocols with 5 × 3 Gy/week, given over one (days 0–4) or two (days 0–4, 7–11) weeks. All fractionation protocols were concluded by a local test irradiation (day 7/14) using graded doses to generate complete dose–effect curves. Daily doses of unfractionated or low molecular weight heparin (40 or 200 I.U./mouse, respectively) were applied subcutaneously over varying time intervals. The incidence and the time course of mucosal ulceration, corresponding to confluent mucositis in patients (RTOG/EORTC grade 3), were analysed as clinically relevant endpoints. RESULTS: Systemic application of heparins significantly increased the iso-effective doses for the induction of mucosal ulceration, particularly in combination with fractionated irradiation protocols. Moreover, a tentative prolongation of the latent time and a pronounced reduction of the ulcer duration were observed. CONCLUSION: These data provide the first evidence for a protective and/or mitigative effect of heparins for radiation-induced oral mucositis. Further studies are ongoing investigating the underlying mechanism. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00066-018-1300-8) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2018-04-16 2018 /pmc/articles/PMC6008356/ /pubmed/29663036 http://dx.doi.org/10.1007/s00066-018-1300-8 Text en © The Author(s) 2018 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 Kowaliuk, Maria Bozsaky, Eva Gruber, Sylvia Kuess, Peter Dörr, Wolfgang Systemic administration of heparin ameliorates radiation-induced oral mucositis—preclinical studies in mice |
title | Systemic administration of heparin ameliorates radiation-induced oral mucositis—preclinical studies in mice |
title_full | Systemic administration of heparin ameliorates radiation-induced oral mucositis—preclinical studies in mice |
title_fullStr | Systemic administration of heparin ameliorates radiation-induced oral mucositis—preclinical studies in mice |
title_full_unstemmed | Systemic administration of heparin ameliorates radiation-induced oral mucositis—preclinical studies in mice |
title_short | Systemic administration of heparin ameliorates radiation-induced oral mucositis—preclinical studies in mice |
title_sort | systemic administration of heparin ameliorates radiation-induced oral mucositis—preclinical studies in mice |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6008356/ https://www.ncbi.nlm.nih.gov/pubmed/29663036 http://dx.doi.org/10.1007/s00066-018-1300-8 |
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