Reduced Pancreatic Exocrine Function and Organellar Disarray in a Canine Model of Acute Pancreatitis

PLoS One. 2016 Feb 19;11(2):e0148458. doi: 10.1371/journal.pone.0148458. eCollection 2016.

Abstract

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.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acute Disease
  • Amylases / biosynthesis
  • Amylases / blood
  • Animals
  • Bicarbonates / metabolism
  • Disease Models, Animal
  • Dogs
  • Extracellular Fluid / metabolism
  • Lipase / biosynthesis
  • Lipase / blood
  • Organelles / metabolism*
  • Organelles / pathology
  • Organelles / ultrastructure
  • Pancreas, Exocrine / metabolism*
  • Pancreas, Exocrine / pathology*
  • Pancreas, Exocrine / ultrastructure
  • Pancreatitis / blood
  • Pancreatitis / metabolism*
  • Pancreatitis / pathology*

Substances

  • Bicarbonates
  • Lipase
  • Amylases

Grants and funding

This work was funded by the Zhejiang Provincial Natural Science Foundation of China (No. LY12H03007), China National Natural Science Foundation (No. 81370563), Ministry of Health of China (No. WKJ2012-2-033), and Public Welfare Technology application research project supported by Science Technology Department of Zhejiang province (No. 2012C23108).