CFTR inhibition augments NHE3 activity during luminal high CO2 exposure in rat duodenal mucosa

American Journal of Physiology - Gastrointestinal and Liver Physiology

Volumn 294, Issue 6, 2008, Pages

  Mizumori, Misa ^b,d   Choi, Yuri ^e   Guth, Paul H ^a   Engel, Eli ^c   Kaunitz, Jonathan D ^a,b   Akiba, Yasutada ^b,d  

^a VA GREATER LOS ANGELES HEALTHCARE SYSTEM   (United States)

^b ROSS UNIVERSITY SCHOOL OF MEDICINE   (United States)

^c UNIVERSITY OF CALIFORNIA   (United States)

^d Brentwood Biomedical Research Institute Los Angeles   (United States)

^e Harvard Westlake School   (United States)

Author keywords

Bicarbonate secretion; CO2 absorption; Portal venous PCO 2

Indexed keywords

4,4' DIISOTHIOCYANATOSTILBENE 2,2' DISULFONIC ACID; BICARBONATE; CARBON DIOXIDE; SODIUM PROTON EXCHANGE PROTEIN; SODIUM PROTON EXCHANGE PROTEIN 3; TRANSMEMBRANE CONDUCTANCE REGULATOR; SODIUM-HYDROGEN EXCHANGER 3;

ACID BASE BALANCE; ANIMAL EXPERIMENT; ANIMAL TISSUE; APICAL MEMBRANE; ARTICLE; CONTROLLED STUDY; DUODENUM MUCOSA; DUODENUM PH; DUODENUM SECRETION; MALE; NONHUMAN; PRIORITY JOURNAL; PROTON SODIUM EXCHANGE; PROTON TRANSPORT; RAT; SMALL INTESTINE ABSORPTION; TRANSPORT KINETICS; ANIMAL; DOSE RESPONSE; DRUG ANTAGONISM; DRUG EFFECT; DUODENUM; INTESTINE MUCOSA; METABOLISM; SPRAGUE DAWLEY RAT;

ANIMALS; CARBON DIOXIDE; CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR; DOSE-RESPONSE RELATIONSHIP, DRUG; DUODENUM; INTESTINAL MUCOSA; MALE; RATS; RATS, SPRAGUE-DAWLEY; SODIUM-HYDROGEN ANTIPORTER;

EID: 48249150864     PISSN: 01931857     EISSN: 15221547     Source Type: Journal    
DOI: 10.1152/ajpgi.00025.2008     Document Type: Article

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