DCCD (N,N'-dicyclohexylcarbodiimide) inhibits biliary secretion of HCO-3

Scand J Gastroenterol. 1987 Mar;22(2):207-13. doi: 10.3109/00365528708991881.

Abstract

To study whether a proton pump is an integral part of the mechanism responsible for secretin-dependent biliary secretion of HCO-3 ions, the proton pump inhibitor N,N'-dicyclohexylcarbodiimide (DCCD) was systemically administered to six anesthetized, secretin-infused pigs. Because biliary HCO-3 secretion varies with arterial pH, secretion rate was measured at several different arterial pH values, before and after DCCD (25 mumol/kg). At arterial pH 7.45, bile flow was 2.1 (1.6-2.9) ml/min, and HCO-3 secretion was 224 (157-311) mumol/min. DCCD reduced bile flow and HCO-3 secretion by 30% and 40%, respectively, independent of arterial pH. In contrast, bile acid secretion, 46 (41-59) mumol/min, was not changed by DCCD. The hepatic adenosine triphosphatase (ATP) level, 2.0 (1.8-2.1) mumol/g wet tissue, was not changed by DCCD. DCCD (10(-4) mol/l) affected neither Na,K-ATPase nor carbonic anhydrase activities in separate in vitro assay systems. The reduction in biliary HCO-3 secretion induced by the proton pump inhibitor DCCD may indicate that a proton pump is integrated into the mechanism responsible for secretin-dependent biliary secretion of HCO-3.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenosine Triphosphate / metabolism
  • Animals
  • Bicarbonates / metabolism*
  • Bile Acids and Salts / metabolism
  • Bile Ducts / metabolism*
  • Carbodiimides / pharmacology*
  • Carbonic Anhydrases / metabolism
  • Dicyclohexylcarbodiimide / pharmacology*
  • Hemodynamics / drug effects
  • Liver / metabolism
  • Protons
  • Secretory Rate / drug effects
  • Sodium-Potassium-Exchanging ATPase / metabolism
  • Swine

Substances

  • Bicarbonates
  • Bile Acids and Salts
  • Carbodiimides
  • Protons
  • Dicyclohexylcarbodiimide
  • Adenosine Triphosphate
  • Carbonic Anhydrases
  • Sodium-Potassium-Exchanging ATPase