Literature DB >> 6202931

General and selective inhibition of pancreatic enzyme discharge using a proteinase inhibitor (FOY-305).

G Adler, U Rausch, F Weidenbach, R Arnold, H F Kern.   

Abstract

The guanidino acid esters (FOY, FOY-305) represent a new class of potent proteinase inhibitors and are thought to have a beneficial effect on the course of acute pancreatitis. Because of their structure and low molecular size they might enter cells and interfere with cellular processes. To test this possibility in the case of the exocrine pancreas a series of in vivo and in vitro studies was carried out to analyse intracellular transport and discharge of pancreatic enzymes in the presence of FOY-305. The infusion of FOY-305 to conscious rats led to a transient inhibition of protein and enzyme discharge from the cannulated pancreas accompanied by lower serum enzyme levels and increased enzyme content in the pancreas. An identical inhibition of discharge of newly synthesized proteins was observed in vitro in the presence of 1 microM FOY-305. The analysis of the release of individual enzymes using separation on two-dimensional gels showed a pronounced inhibition of mainly the release of acidic proteins. FOY-305 not only interfered with discharge of serine proteinases (trypsinogen, chymotrypsinogen, proelastase) but also with procarboxypeptidases and lipase. It was concluded that FOY-305 enters the acinar cell and due to an unspecific binding to acidic proteins interferes with the intracellular transport of individual enzyme proteins during their passage through the membrane-bound cellular compartments. This charge-dependent effect is independent of the inhibitory effect on enzymatic activity of serine proteinases.

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Year:  1984        PMID: 6202931     DOI: 10.1007/bf01742297

Source DB:  PubMed          Journal:  Klin Wochenschr        ISSN: 0023-2173


  16 in total

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Authors:  G A Scheele
Journal:  J Biol Chem       Date:  1975-07-25       Impact factor: 5.157

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Authors:  W Bieger; A Martin-Achard; M Bassler; H F Kern
Journal:  Cell Tissue Res       Date:  1976-01-28       Impact factor: 5.249

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Authors:  M Muramatu; S Fujii
Journal:  Biochim Biophys Acta       Date:  1972-04-07

5.  Modifications of the diphenylamine reaction giving increased sensitivity and simplicity in the estimation of DNA.

Authors:  G M Richards
Journal:  Anal Biochem       Date:  1974-02       Impact factor: 3.365

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Authors:  S Takasugi; H Yonezawa; N Ikei; T Kanno
Journal:  Digestion       Date:  1982       Impact factor: 3.216

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Journal:  Lancet       Date:  1977-09-24       Impact factor: 79.321

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Authors:  G Adler; G Rohr; H F Kern
Journal:  Dig Dis Sci       Date:  1982-11       Impact factor: 3.199

9.  Effects of in vivo cholinergic stimulation of rat exocrine pancreas.

Authors:  G Adler; G Gerhards; J Schick; G Rohr; H F Kern
Journal:  Am J Physiol       Date:  1983-06

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Authors:  G Scheele; R Jacoby; T Carne
Journal:  J Cell Biol       Date:  1980-12       Impact factor: 10.539

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  8 in total

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2.  Stimulation of pancreatic secretory process in the rat by low-molecular weight proteinase inhibitor. II. Regulation of total protein and individual enzyme biosynthesis.

Authors:  U Rausch; H Weidenbach; G Adler; H F Kern
Journal:  Cell Tissue Res       Date:  1987-07       Impact factor: 5.249

3.  Beneficial effects of the synthetic trypsin inhibitor camostate in cerulein-induced acute pancreatitis in rats.

Authors:  M Otsuki; S Tani; Y Okabayashi; M Fuji; T Nakamura; T Fujisawa; H Itoh
Journal:  Dig Dis Sci       Date:  1990-02       Impact factor: 3.199

4.  The effects of nafamostat mesilate (FUT-175) on caerulein-induced acute pancreatitis in the rat.

Authors:  J R Wisner; S Ozawa; I G Renner
Journal:  Int J Pancreatol       Date:  1989-05

5.  Hepatic and pancreatic metabolism and biliary excretion of the protease inhibitor camostat mesilate.

Authors:  K Beckh; H Weidenbach; F Weidenbach; R Müller; G Adler
Journal:  Int J Pancreatol       Date:  1991 Nov-Dec

6.  Chronic oral administration of synthetic trypsin inhibitor camostate reduces amylase release from isolated rat pancreatic acini.

Authors:  M Otsuki; M Fujii; T Nakamura; S Tani; Y Okabayashi
Journal:  Int J Pancreatol       Date:  1995-10

7.  Intracellular action of an exogenous low-molecular-weight synthetic protease inhibitor, E3123, in cerulein-induced acute pancreatitis in rats.

Authors:  N Sata; Y Atomi; W Kimura; A Kuroda; T Muto; C Mineo
Journal:  Int J Pancreatol       Date:  1994-04

8.  Stimulation of pancreatic secretory process in the rat by low-molecular weight proteinase inhibitor. I. Dose-response study on enzyme content and secretion, cholecystokinin release and pancreatic fine structure.

Authors:  U Rausch; G Adler; H Weidenbach; F Weidenbach; D Rudolff; I Koop; H F Kern
Journal:  Cell Tissue Res       Date:  1987-01       Impact factor: 5.249

  8 in total

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