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Local radiotherapy of exposed murine small bowel: Apoptosis and inflammation
BACKGROUND: Preoperative radiotherapy of the pelvic abdomen presents with complications mostly affecting the small bowel. The aim of this study was to define the features of early radiation-induced injury on small bowel. METHODS: 54 mice were divided into two groups (36 irradiated and 18 sham irradi...
Autores principales: | , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2008
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2248567/ https://www.ncbi.nlm.nih.gov/pubmed/18173838 http://dx.doi.org/10.1186/1471-2482-8-1 |
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author | Polistena, Andrea Johnson, Louis Banka Ohiami-Masseron, Salomé Wittgren, Lena Bäck, Sven Thornberg, Charlotte Gadaleanu, Virgil Adawi, Diya Jeppsson, Bengt |
author_facet | Polistena, Andrea Johnson, Louis Banka Ohiami-Masseron, Salomé Wittgren, Lena Bäck, Sven Thornberg, Charlotte Gadaleanu, Virgil Adawi, Diya Jeppsson, Bengt |
author_sort | Polistena, Andrea |
collection | PubMed |
description | BACKGROUND: Preoperative radiotherapy of the pelvic abdomen presents with complications mostly affecting the small bowel. The aim of this study was to define the features of early radiation-induced injury on small bowel. METHODS: 54 mice were divided into two groups (36 irradiated and 18 sham irradiated). Animals were placed on a special frame and (in the radiated group) the exteriorized segment of ileum was subjected to a single absorbed dose of 19 or 38 Gy radiation using 6 MV high energy photons. Specimens were collected for histology, immunohistochemistry (IHC) and ELISA analysis after 2, 24 and 48 hours. Venous blood was collected for systemic leucocyte count in a Burker chamber. RESULTS: Histology demonstrated progressive infiltration of inflammatory cells with cryptitis and increased apoptosis. MIP-2 (macrophage inflammatory protein) concentration was significantly increased in irradiated animals up to 48 hours. No significant differences were observed in IL-10 (interleukin) and TNF-α (tumour necrosis factor) levels. IHC with CD45 showed a significant increase at 2 hours of infiltrating leucocytes and lymphocytes after irradiation followed by progressive decrease with time. Caspase-3 expression increased significantly in a dose dependent trend in both irradiated groups up to 48 hours. CONCLUSION: Acute small bowel injury caused by local irradiation is characterised by increased apoptosis of crypt epithelial cells and by lymphocyte infiltration of the underlying tissue. The severity of histological changes tends to be dose dependent and may affect the course of tissue damage. |
format | Text |
id | pubmed-2248567 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-22485672008-02-21 Local radiotherapy of exposed murine small bowel: Apoptosis and inflammation Polistena, Andrea Johnson, Louis Banka Ohiami-Masseron, Salomé Wittgren, Lena Bäck, Sven Thornberg, Charlotte Gadaleanu, Virgil Adawi, Diya Jeppsson, Bengt BMC Surg Research Article BACKGROUND: Preoperative radiotherapy of the pelvic abdomen presents with complications mostly affecting the small bowel. The aim of this study was to define the features of early radiation-induced injury on small bowel. METHODS: 54 mice were divided into two groups (36 irradiated and 18 sham irradiated). Animals were placed on a special frame and (in the radiated group) the exteriorized segment of ileum was subjected to a single absorbed dose of 19 or 38 Gy radiation using 6 MV high energy photons. Specimens were collected for histology, immunohistochemistry (IHC) and ELISA analysis after 2, 24 and 48 hours. Venous blood was collected for systemic leucocyte count in a Burker chamber. RESULTS: Histology demonstrated progressive infiltration of inflammatory cells with cryptitis and increased apoptosis. MIP-2 (macrophage inflammatory protein) concentration was significantly increased in irradiated animals up to 48 hours. No significant differences were observed in IL-10 (interleukin) and TNF-α (tumour necrosis factor) levels. IHC with CD45 showed a significant increase at 2 hours of infiltrating leucocytes and lymphocytes after irradiation followed by progressive decrease with time. Caspase-3 expression increased significantly in a dose dependent trend in both irradiated groups up to 48 hours. CONCLUSION: Acute small bowel injury caused by local irradiation is characterised by increased apoptosis of crypt epithelial cells and by lymphocyte infiltration of the underlying tissue. The severity of histological changes tends to be dose dependent and may affect the course of tissue damage. BioMed Central 2008-01-03 /pmc/articles/PMC2248567/ /pubmed/18173838 http://dx.doi.org/10.1186/1471-2482-8-1 Text en Copyright © 2008 Polistena et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Polistena, Andrea Johnson, Louis Banka Ohiami-Masseron, Salomé Wittgren, Lena Bäck, Sven Thornberg, Charlotte Gadaleanu, Virgil Adawi, Diya Jeppsson, Bengt Local radiotherapy of exposed murine small bowel: Apoptosis and inflammation |
title | Local radiotherapy of exposed murine small bowel: Apoptosis and inflammation |
title_full | Local radiotherapy of exposed murine small bowel: Apoptosis and inflammation |
title_fullStr | Local radiotherapy of exposed murine small bowel: Apoptosis and inflammation |
title_full_unstemmed | Local radiotherapy of exposed murine small bowel: Apoptosis and inflammation |
title_short | Local radiotherapy of exposed murine small bowel: Apoptosis and inflammation |
title_sort | local radiotherapy of exposed murine small bowel: apoptosis and inflammation |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2248567/ https://www.ncbi.nlm.nih.gov/pubmed/18173838 http://dx.doi.org/10.1186/1471-2482-8-1 |
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