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Duodenal mucosal bicarbonate secretion in pigs is accompanied by compensatory changes in pancreatic and biliary HCO3- secretion

  • Odense Universitetshospital
  • Rigshospitalet

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningpeer review

Abstract

Background: The purpose of the study was to examine the effect of stimulation and inhibition of duodenal mucosal bicarbonate secretion on pancreatic and hepatic bicarbonate secretion in response to acid. Methods: The effect of inhibition (indomethacin) or stimulation (misoprostol) of duodenal mucosal bicarbonate secretion on pancreatic and biliary bicarbonate secretion in response to intraduodenal infusion of HCl or intravenous infusion of secretin was studied in anaesthetized pigs. Results: The hepatic and pancreatic response to exogenous secretin was not significantly altered by stimulation/ inhibition of duodenal bicarbonate secretion. However, pancreatic and biliary bicarbonate secretion in response to duodenal acidification was significantly augmented by inhibition of duodenal mucosal bicarbonate secretion; conversely, it was reduced by stimulation of duodenal bicarbonate secretion. The increase in plasma secretin levels in response to duodenal acidification was reduced by stimulation and augmented by inhibition of duodenal mucosal bicarbonate secretion. Conclusions: Duodenal mucosal bicarbonate secretion can serve as a modulator of both pancreatic and biliary bicarbonate secretion in response to luminal acidification, possibly through regulation of the release of secretin.

OriginalsprogEngelsk
TidsskriftScandinavian Journal of Gastroenterology
Vol/bind29
Udgave nummer10
Sider (fra-til)889-896
ISSN0036-5521
DOI
StatusUdgivet - 1994

Bibliografisk note

Funding Information:
This study was supported by the Danish Medical Research Council (grant 12-9810), P. Carl Petersen’s Fond, and The Foundation of 17-12-1981. The skilful assistance of Karin Sejersen and Sofie Eckhardt is gratefully acknowledged. The authors are grateful to Dr. Jon I. Isenberg and Daniel L. Hogan for revising the manuscript.

Finansiering

This study was supported by the Danish Medical Research Council (grant 12-9810), P. Carl Petersen’s Fond, and The Foundation of 17-12-1981. The skilful assistance of Karin Sejersen and Sofie Eckhardt is gratefully acknowledged. The authors are grateful to Dr. Jon I. Isenberg and Daniel L. Hogan for revising the manuscript.

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