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Reduced Pancreatic Exocrine Function and Organellar Disarray in a Canine Model of Acute Pancreatitis
The aim of the present study was to investigate the pancreatic exocrine function in a canine model and to analyze the changes in organelles of pancreatic acinar cells during the early stage of acute pancreatitis (AP). AP was induced by retrograde injection of 5% sodium taurocholate (0.5 ml/kg) into...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4760769/ https://www.ncbi.nlm.nih.gov/pubmed/26895040 http://dx.doi.org/10.1371/journal.pone.0148458 |
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author | Jin, Yuepeng Bai, Yongyu Li, Qiang Bhugul, Pravin Avinash Huang, Xince Liu, Lewei Pan, Liangliang Ni, Haizhen Chen, Bicheng Sun, Hongwei Zhang, Qiyu Hehir, Michael Zhou, Mengtao |
author_facet | Jin, Yuepeng Bai, Yongyu Li, Qiang Bhugul, Pravin Avinash Huang, Xince Liu, Lewei Pan, Liangliang Ni, Haizhen Chen, Bicheng Sun, Hongwei Zhang, Qiyu Hehir, Michael Zhou, Mengtao |
author_sort | Jin, Yuepeng |
collection | PubMed |
description | The aim of the present study was to investigate the pancreatic exocrine function in a canine model and to analyze the changes in organelles of pancreatic acinar cells during the early stage of acute pancreatitis (AP). AP was induced by retrograde injection of 5% sodium taurocholate (0.5 ml/kg) into the main pancreatic duct of dogs. The induction of AP resulted in serum hyperamylasemia and a marked reduction of amylase activity in the pancreatic fluid (PF). The pancreatic exocrine function was markedly decreased in subjects with AP compared with the control group. After the induction of AP, histological examination showed acinar cell edema, cytoplasmic vacuolization, fibroblasts infiltration, and inflammatory cell infiltration in the interstitium. Electron micrographs after the induction of AP revealed that most of the rough endoplasmic reticulum (RER) were dilated and that some of the ribosomes were no longer located on the RER. The mitochondria were swollen, with shortened and broken cristae. The present study demonstrated, in a canine model, a reduced volume of PF secretion with decreased enzyme secretion during the early stage of AP. Injury of mitochondria and dilatation and degranulation of RER may be responsible for the reduced exocrine function in AP. Furthermore, the present model and results may be useful for researching novel therapeutic measures in AP. |
format | Online Article Text |
id | pubmed-4760769 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-47607692016-03-07 Reduced Pancreatic Exocrine Function and Organellar Disarray in a Canine Model of Acute Pancreatitis Jin, Yuepeng Bai, Yongyu Li, Qiang Bhugul, Pravin Avinash Huang, Xince Liu, Lewei Pan, Liangliang Ni, Haizhen Chen, Bicheng Sun, Hongwei Zhang, Qiyu Hehir, Michael Zhou, Mengtao PLoS One Research Article The aim of the present study was to investigate the pancreatic exocrine function in a canine model and to analyze the changes in organelles of pancreatic acinar cells during the early stage of acute pancreatitis (AP). AP was induced by retrograde injection of 5% sodium taurocholate (0.5 ml/kg) into the main pancreatic duct of dogs. The induction of AP resulted in serum hyperamylasemia and a marked reduction of amylase activity in the pancreatic fluid (PF). The pancreatic exocrine function was markedly decreased in subjects with AP compared with the control group. After the induction of AP, histological examination showed acinar cell edema, cytoplasmic vacuolization, fibroblasts infiltration, and inflammatory cell infiltration in the interstitium. Electron micrographs after the induction of AP revealed that most of the rough endoplasmic reticulum (RER) were dilated and that some of the ribosomes were no longer located on the RER. The mitochondria were swollen, with shortened and broken cristae. The present study demonstrated, in a canine model, a reduced volume of PF secretion with decreased enzyme secretion during the early stage of AP. Injury of mitochondria and dilatation and degranulation of RER may be responsible for the reduced exocrine function in AP. Furthermore, the present model and results may be useful for researching novel therapeutic measures in AP. Public Library of Science 2016-02-19 /pmc/articles/PMC4760769/ /pubmed/26895040 http://dx.doi.org/10.1371/journal.pone.0148458 Text en © 2016 Jin et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Jin, Yuepeng Bai, Yongyu Li, Qiang Bhugul, Pravin Avinash Huang, Xince Liu, Lewei Pan, Liangliang Ni, Haizhen Chen, Bicheng Sun, Hongwei Zhang, Qiyu Hehir, Michael Zhou, Mengtao Reduced Pancreatic Exocrine Function and Organellar Disarray in a Canine Model of Acute Pancreatitis |
title | Reduced Pancreatic Exocrine Function and Organellar Disarray in a Canine Model of Acute Pancreatitis |
title_full | Reduced Pancreatic Exocrine Function and Organellar Disarray in a Canine Model of Acute Pancreatitis |
title_fullStr | Reduced Pancreatic Exocrine Function and Organellar Disarray in a Canine Model of Acute Pancreatitis |
title_full_unstemmed | Reduced Pancreatic Exocrine Function and Organellar Disarray in a Canine Model of Acute Pancreatitis |
title_short | Reduced Pancreatic Exocrine Function and Organellar Disarray in a Canine Model of Acute Pancreatitis |
title_sort | reduced pancreatic exocrine function and organellar disarray in a canine model of acute pancreatitis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4760769/ https://www.ncbi.nlm.nih.gov/pubmed/26895040 http://dx.doi.org/10.1371/journal.pone.0148458 |
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