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The influence of erythropoietin on apoptosis and fibrosis in the early phase of chronic pancreatitis in rats

INTRODUCTION: Chronic pancreatitis (CP) is a continuing, inflammatory process of the pancreas, characterised by irreversible morphological changes. The identification of pancreatic stellate cells resulted in the development of research on the pathogenesis of CP. Erythropoietin (Epo) regulates the in...

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Autores principales: Kazmierak, Weronika, Korolczuk, Agnieszka, Kurzepa, Jacek, Czechowska, Grażyna, Boguszewska-Czubara, Anna, Madro, Agnieszka
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Termedia Publishing House 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8314426/
https://www.ncbi.nlm.nih.gov/pubmed/34336038
http://dx.doi.org/10.5114/aoms.2020.99800
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author Kazmierak, Weronika
Korolczuk, Agnieszka
Kurzepa, Jacek
Czechowska, Grażyna
Boguszewska-Czubara, Anna
Madro, Agnieszka
author_facet Kazmierak, Weronika
Korolczuk, Agnieszka
Kurzepa, Jacek
Czechowska, Grażyna
Boguszewska-Czubara, Anna
Madro, Agnieszka
author_sort Kazmierak, Weronika
collection PubMed
description INTRODUCTION: Chronic pancreatitis (CP) is a continuing, inflammatory process of the pancreas, characterised by irreversible morphological changes. The identification of pancreatic stellate cells resulted in the development of research on the pathogenesis of CP. Erythropoietin (Epo) regulates the interaction between apoptosis and inflammation of the brain, kidney, and heart muscle. Erythropoietin receptors were also found in the pancreas, in particular on the islet cells. Our objective was to evaluate the influence of Epo on fibrosis and apoptosis in experimental CP. MATERIAL AND METHODS: The experiments were performed on 48 male Wistar rats (250–350 g). The animals were divided into six equal groups (I – control, II – chronic cerulein – induced pancreatitis, III – 1 ml of Epo sc, IV – 0.5 ml of Epo sc, V – CP treated with 1 ml Epo, VI – CP treated with 0.5 ml Epo). The blood for gelatinases and pancreata for the morphological examinations and immunohistochemistry were collected. RESULTS: A slight reduction of interstitial oedema and less severe fibrosis were noticed in the groups treated with Epo. Reduced expression of caspase-3 and α-actin, and a lack of Bcl-2 expression were observed in areas with inflammation. There was no expression of caspase-9 observed in all groups. There were no statistically significant differences between the groups in the activity of gelatinases. CONCLUSIONS: Erythropoietin seems to have the effect of reducing fibrosis and apoptosis in an experimental model of CP.
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spelling pubmed-83144262021-07-31 The influence of erythropoietin on apoptosis and fibrosis in the early phase of chronic pancreatitis in rats Kazmierak, Weronika Korolczuk, Agnieszka Kurzepa, Jacek Czechowska, Grażyna Boguszewska-Czubara, Anna Madro, Agnieszka Arch Med Sci Experimental Research INTRODUCTION: Chronic pancreatitis (CP) is a continuing, inflammatory process of the pancreas, characterised by irreversible morphological changes. The identification of pancreatic stellate cells resulted in the development of research on the pathogenesis of CP. Erythropoietin (Epo) regulates the interaction between apoptosis and inflammation of the brain, kidney, and heart muscle. Erythropoietin receptors were also found in the pancreas, in particular on the islet cells. Our objective was to evaluate the influence of Epo on fibrosis and apoptosis in experimental CP. MATERIAL AND METHODS: The experiments were performed on 48 male Wistar rats (250–350 g). The animals were divided into six equal groups (I – control, II – chronic cerulein – induced pancreatitis, III – 1 ml of Epo sc, IV – 0.5 ml of Epo sc, V – CP treated with 1 ml Epo, VI – CP treated with 0.5 ml Epo). The blood for gelatinases and pancreata for the morphological examinations and immunohistochemistry were collected. RESULTS: A slight reduction of interstitial oedema and less severe fibrosis were noticed in the groups treated with Epo. Reduced expression of caspase-3 and α-actin, and a lack of Bcl-2 expression were observed in areas with inflammation. There was no expression of caspase-9 observed in all groups. There were no statistically significant differences between the groups in the activity of gelatinases. CONCLUSIONS: Erythropoietin seems to have the effect of reducing fibrosis and apoptosis in an experimental model of CP. Termedia Publishing House 2020-10-12 /pmc/articles/PMC8314426/ /pubmed/34336038 http://dx.doi.org/10.5114/aoms.2020.99800 Text en Copyright: © 2020 Termedia & Banach https://creativecommons.org/licenses/by-nc-sa/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) License, allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material, provided the original work is properly cited and states its license.
spellingShingle Experimental Research
Kazmierak, Weronika
Korolczuk, Agnieszka
Kurzepa, Jacek
Czechowska, Grażyna
Boguszewska-Czubara, Anna
Madro, Agnieszka
The influence of erythropoietin on apoptosis and fibrosis in the early phase of chronic pancreatitis in rats
title The influence of erythropoietin on apoptosis and fibrosis in the early phase of chronic pancreatitis in rats
title_full The influence of erythropoietin on apoptosis and fibrosis in the early phase of chronic pancreatitis in rats
title_fullStr The influence of erythropoietin on apoptosis and fibrosis in the early phase of chronic pancreatitis in rats
title_full_unstemmed The influence of erythropoietin on apoptosis and fibrosis in the early phase of chronic pancreatitis in rats
title_short The influence of erythropoietin on apoptosis and fibrosis in the early phase of chronic pancreatitis in rats
title_sort influence of erythropoietin on apoptosis and fibrosis in the early phase of chronic pancreatitis in rats
topic Experimental Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8314426/
https://www.ncbi.nlm.nih.gov/pubmed/34336038
http://dx.doi.org/10.5114/aoms.2020.99800
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