Bicarbonate-dependent chloride absorption in small intestine: Ion fluxes and intracellular chloride activities

Summary Proximal, stripped segments of small intestine from the urodeleAmphiuma were short-circuited in media containing Na⁺, Cl^– and HCO ₃ ^– . Under these conditions there was a large net absorption of Cl^–, a small net absorption of Na⁺ and a residual flux (J _Net ^R ) consistent with HCO ₃ ^– secretion. Net Cl^– absorption correlated with the short-circuit current (I _sc); net Na⁺ absorption correlated negatively withJ _Net ^R . Acetazolamide eliminated theI _sc, lowered Cl^– absorption by 50%, and reduced net Na⁺ absorption without alteringJ _Net ^R . Benzolamide inhibited theI _sc without alteringJ _Net ^R . Benzolamide inhibited theI _sc more rapidly when applied on the mucosal surface. Replacement of Na⁺ or HCO ₃ ^– (and CO₂) in the media eliminated theI _sc, net Cl^– absorption and the residual flux. Likewise, inclusion of the stilbene SITS in the serosal media eliminated theI _sc, net Cl^– absorption and the residual flux. The cytoplasmic activity of Cl^– (a _ci ^a ) was determined with single and double-barreled microelectrodes. Thea _ci ^a of villus absorptive cells in normal media was 21.0mm and in excess of that expected on the basis of electrochemical equilibrium of Cl^– at the mucosal membrane. Active Cl^– accumulation was also observed in the presence of acetazolamide but was eliminated upon replacement of media Na⁺ with choline. The mucosal membrane potential was depolarized upon replacement of media Na⁺. It is concluded that Cl^– is actively absorbed into intestinal cells ofAmphiuma by an electrogenic process located in the mucosal membrane. Depending on the level of intracellular HCO ₃ ^– , accumulated Cl^– may diffuse passively back into the mucosal media or undergo exchange with bath HCO ₃ ^– at the serosal membrane.