Literature DB >> 2578923

Exocrine pancreatic function in rats after acute trypsin inhibitor treatment.

M Otsuki, A Ohki, C Sakamoto, Y Okabayashi, S Baba.   

Abstract

A single oral dose of synthetic trypsin inhibitor (TI, 20 mg/100 g) was given to rats by orogastric tube 6, 12, 18, or 24 hr before the removal of the pancreas and the preparation of isolated perfused pancreas. TI treatment induced no significant changes in body weight and total amount of DNA content in the pancreas, but pancreatic wet weight, total pancreatic protein and amylase, and the concentration of total protein and amylase relative to DNA were significantly decreased at 6 or 12 hr posttreatment, with a partial return toward control values at 18-24 hr after TI treatment. In isolated perfused pancreas, basal amylase output was similar in the control and in all 4 groups of TI-pretreated rats, while basal rate of flow of pancreatic juice was significantly increased at 12-24 hr posttreatment. Caerulein (0.1 ng/ml; 64 pM) stimulated pancreatic juice flow was greatly increased in rats pretreated with TI 12-24 hr earlier. In contrast, caerulein-stimulated amylase output was significantly lower in TI-pretreated groups compared with the control. However, when amylase output was related to the total content in the pancreas, the secretory responsiveness for amylase release was significantly higher in rats at 6-18 hr posttreatment compared with the control. The present study indicates that a single oral administration of TI modulates biological response to caerulein in the isolated perfused pancreas. The enhanced responsiveness of amylase release to subsequent stimulation is seen in early periods, while that of pancreatic juice flow is observed in late periods.

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Year:  1985        PMID: 2578923     DOI: 10.1007/bf01347895

Source DB:  PubMed          Journal:  Dig Dis Sci        ISSN: 0163-2116            Impact factor:   3.199


  21 in total

1.  Chymotrypsinogen in the intestine of rats fed soybean trypsin inhibitor and its inability to suppress pancreatic enzyme secretions.

Authors:  R L Lyman; B A Olds; G M Green
Journal:  J Nutr       Date:  1974-01       Impact factor: 4.798

2.  Feedback regulation of pancreatic enzyme secretion as a mechanism for trypsin inhibitor-induced hypersecretion in rats.

Authors:  G M Green; R L Lyman
Journal:  Proc Soc Exp Biol Med       Date:  1972-05

3.  A new and rapid method for the clinical determination of alpha-amylase activities in human serum and urine. Optimal conditions.

Authors:  M Ceska; K Birath; B Brown
Journal:  Clin Chim Acta       Date:  1969-12       Impact factor: 3.786

4.  An improved fluorometric assay for DNA.

Authors:  R T Hinegardner
Journal:  Anal Biochem       Date:  1971-01       Impact factor: 3.365

5.  Trypsin as a regulator of pancreatic secretion in the rat.

Authors:  I Ihse; P Lilja; I Lundquist
Journal:  Scand J Gastroenterol       Date:  1979       Impact factor: 2.423

6.  Amylase secretion by isolated pancreatic acini after acute cholecystokinin treatment in vivo.

Authors:  M Otsuki; Y Okabayashi; A Ohki; S R Hootman; S Baba; J A Williams
Journal:  Am J Physiol       Date:  1984-04

7.  Secretion of rat pancreas perfused with plasma from rats fed soybean trypsin inhibitor.

Authors:  H Khayambashi; R L Lyman
Journal:  Am J Physiol       Date:  1969-09

8.  Glucose-dependent insulinotropic action of cholecystokinin and caerulein in the isolated perfused rat pancreas.

Authors:  C Sakamoto; M Otsuki; A Ohki; H Yuu; M Maeda; T Yamasaki; S Baba
Journal:  Endocrinology       Date:  1982-02       Impact factor: 4.736

9.  Amylase secretion by isolated pancreatic acini after chronic cholecystokinin treatment in vivo.

Authors:  M Otsuki; J A Williams
Journal:  Am J Physiol       Date:  1983-06

10.  The release of rat intestinal cholecystokinin after oral trypsin inhibitor measured by bio-assay.

Authors:  S J Brand; R G Morgan
Journal:  J Physiol       Date:  1981       Impact factor: 5.182

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  4 in total

1.  Histologic and biochemical alterations in experimental acute pancreatitis induced by supramaximal caerulein stimulation.

Authors:  S Tani; M Otsuki; H Itoh; M Fujii; T Nakamura; T Oka; S Baba
Journal:  Int J Pancreatol       Date:  1987 Oct-Dec

2.  Elevation of resting fluid secretion precedes trophic responses in the rat pancreas following a single oral administration of Camostat.

Authors:  K Terasawa; T Kanno
Journal:  Int J Pancreatol       Date:  1991-04

3.  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

4.  Effects of secretin and caerulein on luminal feedback regulation of pancreatic enzyme secretion in rats.

Authors:  K Kataoka
Journal:  Gastroenterol Jpn       Date:  1988-04
  4 in total

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