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Novel Peritoneal Sclerosis Rat Model Developed by Administration of Bleomycin and Lansoprazole

In our preliminary experiment, peritoneal sclerosis likely induced by peritoneal dialysis was unexpectedly observed in the livers of rats given bleomycin and lansoprazole. We examined whether this peritoneal thickening around the liver was time-dependently induced by administration of both drugs. Ma...

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Autores principales: Kunitatsu, Kosei, Yamamoto, Yuta, Nasu, Shota, Taniji, Akira, Kawashima, Shuji, Yamagishi, Naoko, Ito, Takao, Inoue, Shigeaki, Kanai, Yoshimitsu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10671295/
https://www.ncbi.nlm.nih.gov/pubmed/38003303
http://dx.doi.org/10.3390/ijms242216108
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author Kunitatsu, Kosei
Yamamoto, Yuta
Nasu, Shota
Taniji, Akira
Kawashima, Shuji
Yamagishi, Naoko
Ito, Takao
Inoue, Shigeaki
Kanai, Yoshimitsu
author_facet Kunitatsu, Kosei
Yamamoto, Yuta
Nasu, Shota
Taniji, Akira
Kawashima, Shuji
Yamagishi, Naoko
Ito, Takao
Inoue, Shigeaki
Kanai, Yoshimitsu
author_sort Kunitatsu, Kosei
collection PubMed
description In our preliminary experiment, peritoneal sclerosis likely induced by peritoneal dialysis was unexpectedly observed in the livers of rats given bleomycin and lansoprazole. We examined whether this peritoneal thickening around the liver was time-dependently induced by administration of both drugs. Male Wistar rats were injected with bleomycin and/or lansoprazole for 2 or 4 weeks. The 3YB-1 cell line derived from rat fibroblasts was treated by bleomycin and/or lansoprazole for 24 h. The administration of both drugs together, but not individually, thickened the peritoneal tissue around the liver. There was accumulation of collagen fibers, macrophages, and eosinophils under mesothelial cells. Expressions of Col1a1, Mcp1 and Mcp3 genes were increased in the peritoneal tissue around the liver and in 3YB-1 cells by the administration of both drugs together, and Opn genes had increased expressions in this tissue and 3YB-1 cells. Mesothelial cells indicated immunoreactivity against both cytokeratin, a mesothelial cell marker, and αSMA, a fibroblast marker, around the livers of rats given both drugs. Administration of both drugs induced the migration of macrophages and eosinophils and induced fibrosis associated with the possible activation of fibroblasts and the possible promotion of the mesothelial–mesenchymal transition. This might become a novel model of peritoneal sclerosis for peritoneal dialysis.
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spelling pubmed-106712952023-11-09 Novel Peritoneal Sclerosis Rat Model Developed by Administration of Bleomycin and Lansoprazole Kunitatsu, Kosei Yamamoto, Yuta Nasu, Shota Taniji, Akira Kawashima, Shuji Yamagishi, Naoko Ito, Takao Inoue, Shigeaki Kanai, Yoshimitsu Int J Mol Sci Article In our preliminary experiment, peritoneal sclerosis likely induced by peritoneal dialysis was unexpectedly observed in the livers of rats given bleomycin and lansoprazole. We examined whether this peritoneal thickening around the liver was time-dependently induced by administration of both drugs. Male Wistar rats were injected with bleomycin and/or lansoprazole for 2 or 4 weeks. The 3YB-1 cell line derived from rat fibroblasts was treated by bleomycin and/or lansoprazole for 24 h. The administration of both drugs together, but not individually, thickened the peritoneal tissue around the liver. There was accumulation of collagen fibers, macrophages, and eosinophils under mesothelial cells. Expressions of Col1a1, Mcp1 and Mcp3 genes were increased in the peritoneal tissue around the liver and in 3YB-1 cells by the administration of both drugs together, and Opn genes had increased expressions in this tissue and 3YB-1 cells. Mesothelial cells indicated immunoreactivity against both cytokeratin, a mesothelial cell marker, and αSMA, a fibroblast marker, around the livers of rats given both drugs. Administration of both drugs induced the migration of macrophages and eosinophils and induced fibrosis associated with the possible activation of fibroblasts and the possible promotion of the mesothelial–mesenchymal transition. This might become a novel model of peritoneal sclerosis for peritoneal dialysis. MDPI 2023-11-09 /pmc/articles/PMC10671295/ /pubmed/38003303 http://dx.doi.org/10.3390/ijms242216108 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Kunitatsu, Kosei
Yamamoto, Yuta
Nasu, Shota
Taniji, Akira
Kawashima, Shuji
Yamagishi, Naoko
Ito, Takao
Inoue, Shigeaki
Kanai, Yoshimitsu
Novel Peritoneal Sclerosis Rat Model Developed by Administration of Bleomycin and Lansoprazole
title Novel Peritoneal Sclerosis Rat Model Developed by Administration of Bleomycin and Lansoprazole
title_full Novel Peritoneal Sclerosis Rat Model Developed by Administration of Bleomycin and Lansoprazole
title_fullStr Novel Peritoneal Sclerosis Rat Model Developed by Administration of Bleomycin and Lansoprazole
title_full_unstemmed Novel Peritoneal Sclerosis Rat Model Developed by Administration of Bleomycin and Lansoprazole
title_short Novel Peritoneal Sclerosis Rat Model Developed by Administration of Bleomycin and Lansoprazole
title_sort novel peritoneal sclerosis rat model developed by administration of bleomycin and lansoprazole
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10671295/
https://www.ncbi.nlm.nih.gov/pubmed/38003303
http://dx.doi.org/10.3390/ijms242216108
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