Glutathione and ATP levels, subcellular distribution of enzymes, and permeability of duct system in rabbit pancreas following intravenous administration of alcohol and cerulein

• Published in: Digestive diseases and sciences 1994-04, Vol.39 (4), p.871-879
• Main Authors: LÜTHEN, R. E, NIEDERAU, C, GRENDELL, J. H
• Format: Article
• Language: English
• Subjects: Adenosine Triphosphate - metabolism; Alcoholism - complications; Animals; Biological and medical sciences; Ceruletide - adverse effects; Ethanol - adverse effects; Gastroenterology. Liver. Pancreas. Abdomen; Glutathione - metabolism; Liver. Biliary tract. Portal circulation. Exocrine pancreas; Male; Medical sciences; Other diseases. Semiology; Pancreas - drug effects; Pancreas - enzymology; Pancreas - metabolism; Pancreatic Ducts - metabolism; Pancreatitis - etiology; Pancreatitis - physiopathology; Rabbits
• ISSN: 0163-2116; 1573-2568
• DOI: 10.1007/BF02087436

In order to reproduce what might occur during the initial phase in some cases of acute alcohol-induced pancreatitis, rabbits were infused with diluted ethanol and low-dose cerulein. The duct permeability was assessed by recovery of fluoresceinated dextran (molecular weight 19,500) in central venous blood following orthograde duct perfusion with this substance in the anesthetized animal. Serum ethanol, lipase, and amylase were measured; pancreatic duct morphology was examined by light microscopy and electron microscopy. ATP and glutathione were measured, as were amylase, trypsinogen/trypsin, cathepsin B, and DNA levels in differential centrifugates. As expected, acinar amylase and trypsinogen showed a significant decrease in the experimental group; cathepsin B activity was similarly diminished. Compared with the control group, the activity of serum amylase and lipase in the experimental group demonstrated a significant increase. However, no differences between saline-infused control animals and the treated group regarding pancreatic duct permeability, continuity of lumen-lining epithelium, ATP and glutathione levels, and the relative subcellular distribution of pancreatic digestive and lysosomal enzymes were observed. Thus, our findings do not support the relevance of some of the most common hypotheses on the pathophysiology of acute pancreatitis in its early stage for at least a certain subgroup of patients with acute alcohol-induced pancreatitis.