1. Effect of inhibitors of gastric secretion on polarization of gastric potential by voltage clamping.
- Author
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Carrasquer G, Zhang JY, Wu X, Rehm WS, and Schwartz M
- Subjects
- Animals, Famotidine pharmacology, Gastric Mucosa drug effects, In Vitro Techniques, Kinetics, Membrane Potentials, Models, Biological, Omeprazole pharmacology, Potassium pharmacology, Rana pipiens, Sodium Chloride pharmacology, Sodium-Potassium-Exchanging ATPase metabolism, Stomach drug effects, Gastric Acid metabolism, Gastric Mucosa physiology, Stomach physiology
- Abstract
Voltage clamping across the frog gastric mucosa, nutrient positive to secretory, results in an increase in the open-circuit potential difference (OCPD). The increase in OCPD, or polarization, induced by voltage clamping could be caused by a redistribution of ions across the plasma membrane or by a polarization of pump electromotive forces, such as the Na(+)-K(+)-adenosinetriphosphatase (ATPase) located in the nutrient (serosal) membrane or the proton pump located in the secretory (luminal) membrane. The polarization induced by voltage clamping was not affected by removing Cl- and Na+ or by increasing the K+ concentration to 79 mM but was markedly reduced by placing in the nutrient solution 10(-3) M famotidine or 10(-4) M omeprazole. These data suggest that there is a strong contribution of the proton pump to the polarization induced by voltage clamping with some contribution of ion redistribution and/or the Na(+)-K(+)-ATPase. The data support the electrogenicity of the proton pump.
- Published
- 1993
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