Literature DB >> 2562834

Effects of somatostatin on hepatic bile formation.

I Magnusson1, K Einarsson, B Angelin, B Nyberg, K Bergström, L Thulin.   

Abstract

Somatostatin is a peptide that has anticholeretic properties in the dog. The purpose of the present work was to investigate if somatostatin is an anticholeretic agent in humans also. The effects of intravenous infusion of somatostatin on hepatic bile flow and biliary electrolytes and secretion of biliary lipids were studied in 7 patients with complete biliary drainage who had been operated on for choledocholithiasis. Somatostatin, 250 microgram/h, was found to decrease the hepatic bile secretion by approximately 30%. The peptide also reduced the outputs of bile acids, cholesterol, and phospholipids and the outputs of sodium, potassium, and chloride. The concentrations of the biliary lipids were not significantly changed. Somatostatin inhibited the erythritol clearance in the 2 patients studied by approximately 25%. The present study thus provides evidence that somatostatin inhibits bile formation in humans. It appears as if the reduction in bile production is mainly due to decreased canalicular bile flow. It is possible that this effect of somatostatin is attributable to inhibition of bile acid synthesis or of transport-secretion of bile acids, or both.

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Year:  1989        PMID: 2562834     DOI: 10.1016/0016-5085(89)90782-8

Source DB:  PubMed          Journal:  Gastroenterology        ISSN: 0016-5085            Impact factor:   22.682


  12 in total

1.  Bile acid formation in primary human hepatocytes.

Authors:  Curt Einarsson; Ewa Ellis; Anna Abrahamsson; Bo-Goran Ericzon; Ingermar Bjorkhem; Magnus Axelson
Journal:  World J Gastroenterol       Date:  2000-08       Impact factor: 5.742

2.  Cholescintigraphic study of effect of somatostatin analog, octreotide, on bile secretion and gallbladder emptying in normal subjects.

Authors:  C Grimaldi; J Darcourt; A G Harris; E Lebot; F Lapalus; J Delmont
Journal:  Dig Dis Sci       Date:  1993-09       Impact factor: 3.199

3.  Hepatolithiasis (intrahepatic stone) during octreotide therapy for acromegaly: a case report.

Authors:  M T Sheehan; T B Nippoldt
Journal:  Pituitary       Date:  2000-12       Impact factor: 4.107

4.  The effect of plasma low density lipoprotein apheresis on the hepatic secretion of biliary lipids in humans.

Authors:  C G Hillebrant; B Nyberg; K Einarsson; M Eriksson
Journal:  Gut       Date:  1997-11       Impact factor: 23.059

Review 5.  Drug-induced gallbladder disease. Incidence, aetiology and management.

Authors:  P P Michielsen; H Fierens; Y M Van Maercke
Journal:  Drug Saf       Date:  1992 Jan-Feb       Impact factor: 5.606

6.  Effect of octreotide on gall stone prevalence and gall bladder motility in acromegaly.

Authors:  S M Catnach; J V Anderson; P D Fairclough; R C Trembath; P A Wilson; E Parker; G M Besser; J A Wass
Journal:  Gut       Date:  1993-02       Impact factor: 23.059

7.  Postprandial gall bladder motility and hormone release during intermittent and continuous subcutaneous octreotide treatment in acromegaly.

Authors:  M F Stolk; K J van Erpecum; H P Koppeschaar; W I de Bruin; J B Jansen; C B Lamers; G P van Berge Henegouwen
Journal:  Gut       Date:  1993-06       Impact factor: 23.059

8.  Postprandial gallbladder motility and plasma cholecystokinin at regular time intervals after injection of octreotide in acromegalics on long-term treatment.

Authors:  W P Hopman; P A Van Liessum; G F Pieters; J B Jansen; C B Lamers; A G Smals; G Rosenbusch; P W Kloppenborg
Journal:  Dig Dis Sci       Date:  1992-11       Impact factor: 3.199

9.  Pancreatic polypeptide inhibits somatostatin secretion.

Authors:  Wook Kim; Jennifer L Fiori; Yu-Kyong Shin; Eitan Okun; Jung Seok Kim; Peter R Rapp; Josephine M Egan
Journal:  FEBS Lett       Date:  2014-07-11       Impact factor: 4.124

10.  Effect of chronic octreotide treatment on intestinal absorption in patients with acromegaly.

Authors:  P J Ho; L D Boyajy; E Greenstein; A L Barkan
Journal:  Dig Dis Sci       Date:  1993-02       Impact factor: 3.199

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