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Cellular bicarbonate protects rat duodenal mucosa from acid-induced injury
Yasutada Akiba, … , Ira Kurtz, Jonathan D. Kaunitz
Yasutada Akiba, … , Ira Kurtz, Jonathan D. Kaunitz
Published December 15, 2001
Citation Information: J Clin Invest. 2001;108(12):1807-1816. https://doi.org/10.1172/JCI12218.
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Article

Cellular bicarbonate protects rat duodenal mucosa from acid-induced injury

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Abstract

Secretion of bicarbonate from epithelial cells is considered to be the primary mechanism by which the duodenal mucosa is protected from acid-related injury. Against this view is the finding that patients with cystic fibrosis, who have impaired duodenal bicarbonate secretion, are paradoxically protected from developing duodenal ulcers. Therefore, we hypothesized that epithelial cell intracellular pH regulation, rather than secreted extracellular bicarbonate, was the principal means by which duodenal epithelial cells are protected from acidification and injury. Using a novel in vivo microscopic method, we have measured bicarbonate secretion and epithelial cell intracellular pH (pHi), and we have followed cell injury in the presence of the anion transport inhibitor DIDS and the Cl– channel inhibitor, 5-nitro-2-(3-phenylpropylamino) benzoic acid (NPPB). DIDS and NPPB abolished the increase of duodenal bicarbonate secretion following luminal acid perfusion. DIDS decreased basal pHi, whereas NPPB increased pHi; DIDS further decreased pHi during acid challenge and abolished the pHi overshoot over baseline observed after acid challenge, whereas NPPB attenuated the fall of pHi and exaggerated the overshoot. Finally, acid-induced epithelial injury was enhanced by DIDS and decreased by NPPB. The results support the role of intracellular bicarbonate in the protection of duodenal epithelial cells from luminal gastric acid.

Authors

Yasutada Akiba, Osamu Furukawa, Paul H. Guth, Eli Engel, Igor Nastaskin, Pejvak Sassani, Ramanath Dukkipatis, Alexander Pushkin, Ira Kurtz, Jonathan D. Kaunitz

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