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Animal Models of Chronic Pancreatitis
Animal models for CP in rats can be classified into 2 groups: one is noninvasive or nonsurgical models and the other is invasive or surgical models. Pancreatic injury induced by repetitive injections of supramaximal stimulatory dose of caerulein (Cn) or by intraductal infusion of sodium taurocholate...
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Formato: | Texto |
Lenguaje: | English |
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Hindawi Publishing Corporation
2010
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3010641/ https://www.ncbi.nlm.nih.gov/pubmed/21197438 http://dx.doi.org/10.1155/2010/403295 |
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author | Otsuki, Makoto Yamamoto, Mitsuyoshi Yamaguchi, Taizo |
author_facet | Otsuki, Makoto Yamamoto, Mitsuyoshi Yamaguchi, Taizo |
author_sort | Otsuki, Makoto |
collection | PubMed |
description | Animal models for CP in rats can be classified into 2 groups: one is noninvasive or nonsurgical models and the other is invasive or surgical models. Pancreatic injury induced by repetitive injections of supramaximal stimulatory dose of caerulein (Cn) or by intraductal infusion of sodium taurocholate (NaTc) recovered within 14 days, whereas that caused by repetitive injection of arginine or by intraductal infusion of oleic acid was persistent. However, the destroyed acinar tissues were replaced by fatty tissues without fibrosis. Transient stasis of pancreatic fluid flow by 0.01% agarose and minimum injury of the pancreatic duct by 0.1% NaTc solution induced progressive pancreatic injury although one alone is insufficient to cause persistent pancreatic injury. However, the damaged tissue was replaced by fatty tissue without fibrosis. Continuous pancreatic ductal hypertension (PDH) caused diffuse interlobular and intralobular fibrosis closely resembling human CP. |
format | Text |
id | pubmed-3010641 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-30106412010-12-30 Animal Models of Chronic Pancreatitis Otsuki, Makoto Yamamoto, Mitsuyoshi Yamaguchi, Taizo Gastroenterol Res Pract Review Article Animal models for CP in rats can be classified into 2 groups: one is noninvasive or nonsurgical models and the other is invasive or surgical models. Pancreatic injury induced by repetitive injections of supramaximal stimulatory dose of caerulein (Cn) or by intraductal infusion of sodium taurocholate (NaTc) recovered within 14 days, whereas that caused by repetitive injection of arginine or by intraductal infusion of oleic acid was persistent. However, the destroyed acinar tissues were replaced by fatty tissues without fibrosis. Transient stasis of pancreatic fluid flow by 0.01% agarose and minimum injury of the pancreatic duct by 0.1% NaTc solution induced progressive pancreatic injury although one alone is insufficient to cause persistent pancreatic injury. However, the damaged tissue was replaced by fatty tissue without fibrosis. Continuous pancreatic ductal hypertension (PDH) caused diffuse interlobular and intralobular fibrosis closely resembling human CP. Hindawi Publishing Corporation 2010 2010-12-14 /pmc/articles/PMC3010641/ /pubmed/21197438 http://dx.doi.org/10.1155/2010/403295 Text en Copyright © 2010 Makoto Otsuki et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Article Otsuki, Makoto Yamamoto, Mitsuyoshi Yamaguchi, Taizo Animal Models of Chronic Pancreatitis |
title | Animal Models of Chronic Pancreatitis |
title_full | Animal Models of Chronic Pancreatitis |
title_fullStr | Animal Models of Chronic Pancreatitis |
title_full_unstemmed | Animal Models of Chronic Pancreatitis |
title_short | Animal Models of Chronic Pancreatitis |
title_sort | animal models of chronic pancreatitis |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3010641/ https://www.ncbi.nlm.nih.gov/pubmed/21197438 http://dx.doi.org/10.1155/2010/403295 |
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