Biomedical subjects
H Sarles
Publications and source records attributed to H Sarles.
The effects of pentolinium and vagotomy on the inhibition of canine exocrine pancreatic secretion by intravenous ethanol.
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Effects of chronic intragastric ethanol administration on canine exocrine pancreatic secretion.
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Presence of colipase in a congenital pancreatic lipase deficiency.
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Inhibitory action of alcohol on human exocrine pancreatic secretion.
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[Controlled study of the action of maintenance therapy between attacks of duodenal ulcer].
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[An experience in computerized medical records in gastroenterology].
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[Pathogenesis and geographic distribution of chronic pancreatitis].
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[The effects of atropine, penthonium, vagotomy and fluothane on pancreatic secretion in dogs].
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[Chronic primary calcifying pancreatitis. (Apropos of 150 cases)].
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Three-dimensional reconstruction of the pancreatic ducts in chronic pancreatitis.
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[Different action of short, medium, and long chain triglycerides on exocrine pancreatic secretion in man].
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Alcohol and chronic pancreatitis.
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[Comparison of the proteins in pancreatic juice in normal and diseased humans. Determination of serum proteins and demonstration of a particular protein in chronic calcifying pancreatitis].
For a better understanding of the molecular mechanism leading to intraductal precipitation of proteins in primary chronic calcifying pancreatitis in man, we studied the composition of normal and pathological human pancreatic juice by immunotechniques. We found an increased level of serum proteins in pathological juices: 12.47% of total proteins compared to 1.8% in normal ones; albumin is 8.16% of the total proteins, IgG 2.84%, IgA 0.83% and IgM 0.91%. Transferrin and alpha 2-macroglobulin are present, but were not estimated. The albumin/IgA and albumin/IgG ratios favour the hypothesis of a local synthesis of these immunoglobulins as was shown in normal juice. The cross adsorption of antisera against pancreatic juice showed the presence in the pathological juice of a normal molecule in much higher concentration. The role of these proteins in precipitation is discussed.
[Albumin, IgG and IgA in normal adult human pancreatic juice].
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A comparison of alcoholic pancreatitis in rat and man.
Acute ethanol intoxication was studied in 38 Wistar rats, 18 on a balanced diet and 20 on a high fat diet, fed by gavage on 47% ethanol in a dosage of from 3 to 12 g/kg body weight daily for periods ranging from three to 16 days. No macroscopic changes in pancreas or liver were found in any of these animals. Histological changes (venous congestion of the pancreas, the liver, and the kidneys) were found in rats given 4 g or more per kilogram. The only difference between the findings in rats given a balanced diet and those given a high fat diet was the development of fatty livers in the latter group. Chronic ethanol intoxication was studied in 45 Wistar rats, on a balanced diet, which were given 20% ethanol freely for 20 to 30 months. More than half the animals developed pancreatic lesions very similar to those of human chronic pancreatitis. The pathological changes, in foci surrounded by normal pancreatic tissue, were a reduction in acini, duct multiplication (probably by neogenesis), protein plugs, sometimes calcified in the ducts and sclerosis. Samples of pancreatic juice from four animals exposed to ethanol contained significantly higher protein concentrations than samples taken from two control animals. Protein precipitates appeared spontaneously in the pancreatic juice of the animals exposed to ethanol, but not in that of the controls. These findings are very similar to those in alcoholic pancreatitis in man, which has thus been reproduced for the first time in experimental animals. Beta-cell adenomata of the islets of Langerhans were observed in four of the rats exposed to ethanol.
The interaction of ethanol, dietary lipids, and proteins on the rat pancreas. I. Pancreatic enzymes.
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The interaction of ethanol, dietary lipids and proteins on the rat pancreas. II. Ultrastructural study.
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