Literature DB >> 22227376

Radiation-induced damage in different segments of the rat intestine after external beam irradiation of the liver.

Silke Cameron1, Antonia Schwartz, Sadaf Sultan, Inga-Marie Schaefer, Robert Hermann, Margret Rave-Fränk, Clemens F Hess, Hans Christiansen, Giuliano Ramadori.   

Abstract

INTRODUCTION: The out-of-field effects on the intestine, caused by radiation treatment of a parenchymatous organ, have not previously been studied.
METHODS: A single dose of 25Gy was administered percutaneously to the liver of male Wistar rats after a planning CT-scan. Sham-irradiated animals served as controls. At 1, 6, 24, 96h, 1.5 and 3months the duodenum, jejunum, ileum and distal colon were removed, washed and deep-frozen or prepared for paraffin staining.
RESULTS: All animals survived the treatment. Epithelial cell damage occurred in all small-intestinal segments. However, prolonged denudation of the villi together with destruction of the crypt lining was only observed in the ileum, resulting in deficient regeneration. In the colon, changes were minor. Radiation mucositis with granulocyte (MP0+) infiltration was seen from 1 to 24h in the duodenum and jejunum, when ED1+ macrophages, CD3+ T-lymphocytes, and CD34+ hematopoietic precursor cells were recruited, accompanied by an increase in the chemokines MCP-1, MIP-1α, MIP3α and Il-8. In the ileum, early granulocyte infiltration was delayed but continuous. Recruitment of macrophages and lymphocytes was deficient and induction of chemokines as of the adhesion molecules PECAM-1, ICAM-1 was lacking.
CONCLUSION: Post-irradiation damage to the ileum was delayed and followed by an altered repair process with structural changes of the villi. The observed changes might result from a higher sensitivity to oxidative stress mechanisms with subsequent damage of the regenerative capacity of the crypt-villus axis, accompanied by a sustained "inflammatory response" and vascular damage with a lack of regeneratory cell recruitment.
Copyright © 2011 Elsevier Inc. All rights reserved.

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Year:  2011        PMID: 22227376     DOI: 10.1016/j.yexmp.2011.11.007

Source DB:  PubMed          Journal:  Exp Mol Pathol        ISSN: 0014-4800            Impact factor:   3.362


  11 in total

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Authors:  Ashley Purgason; Ye Zhang; Stanley R Hamilton; Daila S Gridley; Ayodotun Sodipe; Olufisayo Jejelowo; Govindarajan T Ramesh; Maria Moreno-Villanueva; Honglu Wu
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2.  FDG-Avid Focal Liver Reaction From Proton Therapy in a Patient With Primary Esophageal Adenocarcinoma.

Authors:  Hena S Ahmed; Austin R Pantel; James M Metz; John P Plastaras; Michael D Farwell
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3.  Matrix metalloproteinase expression is altered in the small and large intestine following fractionated radiation in vivo.

Authors:  Romany L Stansborough; Noor Al-Dasooqi; Emma H Bateman; Joanne M Bowen; Dorothy M K Keefe; Richard M Logan; Ann S J Yeoh; Eric E K Yeoh; Andrea M Stringer; Rachel J Gibson
Journal:  Support Care Cancer       Date:  2018-05-12       Impact factor: 3.603

4.  Rapid disruption of intestinal epithelial tight junction and barrier dysfunction by ionizing radiation in mouse colon in vivo: protection by N-acetyl-l-cysteine.

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Review 6.  Macrophage inflammatory protein-2 as mediator of inflammation in acute liver injury.

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Journal:  PLoS One       Date:  2017-04-12       Impact factor: 3.240

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Authors:  Mohamed T Khayyal; Farouk K El-Baz; Meselhy R Meselhy; Gamila H Ali; Rania M El-Hazek
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9.  Differential regulation of ferritin subunits and iron transport proteins: an effect of targeted hepatic X-irradiation.

Authors:  Naila Naz; Shakil Ahmad; Silke Cameron; Federico Moriconi; Margret Rave-Fränk; Hans Christiansen; Clemens Friedrich Hess; Giuliano Ramadori; Ihtzaz A Malik
Journal:  Biomed Res Int       Date:  2013-12-12       Impact factor: 3.411

10.  Single administration of p2TA (AB103), a CD28 antagonist peptide, prevents inflammatory and thrombotic reactions and protects against gastrointestinal injury in total-body irradiated mice.

Authors:  Salida Mirzoeva; Tatjana Paunesku; M Beau Wanzer; Anat Shirvan; Raymond Kaempfer; Gayle E Woloschak; William Small
Journal:  PLoS One       Date:  2014-07-23       Impact factor: 3.240

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