CFTR and its key role in in vivo resting and luminal acid-induced duodenal HCO3- secretion

Acta Physiol (Oxf). 2008 Aug;193(4):357-65. doi: 10.1111/j.1748-1716.2008.01854.x. Epub 2008 Mar 21.

Abstract

Background and aims: We investigated the role of the recently discovered, villous-expressed anion exchanger Slc26a6 (PAT1) and the predominantly crypt-expressed cystic fibrosis transmembrane regulator (CFTR) in basal and acid-stimulated murine duodenal HCO(3)(-) secretion in vivo, and the influence of blood HCO(3)(-) concentration on both.

Methods: The proximal duodenum of anaesthetized mice was perfused in situ, and HCO(3)(-) secretion was determined by back-titration. Duodenal mucosal permeability was assessed by determining (51)Cr-EDTA leakage from blood to lumen.

Results: Compared with wild type (WT) littermates basal duodenal HCO(3)(-) secretory rates were slightly reduced in Slc26-deficient mice at low ( approximately 21 mm), and markedly reduced at high blood HCO(3)(-) concentration ( approximately 29 mm). In contrast, basal HCO(3)(-) secretion was markedly reduced in CFTR-deficient mice compared with WT littermates both at high and low blood HCO(3)(-) concentration. A short-term application of luminal acid increased duodenal HCO(3)(-) secretory rate in Slc26a6-deficient and WT mice to the same degree, but had no stimulatory effect in the absence of CFTR. Luminal acidification to pH 2.5 did not alter duodenal permeability.

Conclusions: The involvement of Slc26a6 in basal HCO(3)(-) secretion in murine duodenum in vivo is critically dependent on the systemic acid/base status, and this transporter is not involved in acid-stimulated HCO(3)(-) secretion. The presence of CFTR is essential for basal and acid-induced HCO(3)(-) secretion irrespective of acid/base status. This suggests a coupled action of Slc26a6 with CFTR for murine basal duodenal HCO(3)(-) secretion, but not acid-stimulated secretion, in vivo.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antiporters / deficiency
  • Antiporters / physiology
  • Bicarbonates / blood
  • Bicarbonates / metabolism*
  • Cystic Fibrosis Transmembrane Conductance Regulator / deficiency
  • Cystic Fibrosis Transmembrane Conductance Regulator / physiology*
  • Duodenum / metabolism*
  • Hydrogen-Ion Concentration
  • Intestinal Absorption / physiology
  • Intestinal Mucosa / metabolism*
  • Mice
  • Mice, Inbred C57BL
  • Mice, Inbred CFTR
  • Permeability
  • Sulfate Transporters

Substances

  • Antiporters
  • Bicarbonates
  • Slc26a6 protein, mouse
  • Sulfate Transporters
  • Cystic Fibrosis Transmembrane Conductance Regulator