British Journal of Pharmacology · 1986 · 92 citations · 13 references
Life SciencesPharmacologyPhysiologyBioenergeticsCellular BiochemistryEnzymologyEnzyme InhibitionEnzyme KineticsGastrointestinal FunctionGastrointestinal PathophysiologyGastrointestinal PharmacologyGastrointestinal PhysiologyAcid Secretion InhibitionAntisecretory TherapyCompetitive InhibitionGastric EnzymesNa+/k+-atpase FunctionNa-k-atpase ActivitySodium-potassium Adenosine TriphosphataseSodium-potassium Atpase
The mechanism of the gastric antisecretory action of SCH 28080 has been studied utilizing two different in vitro test systems, isolated and enriched parietal cells from the guinea-pig and guinea-pig gastric membranes purified and enriched with K+/H+-ATPase. In guinea-pig isolated and enriched parietal cells SCH 28080 inhibited the acid response to histamine and high K+ concentrations with IC50 values not significantly different from each other. SCH 28080 inhibited the purified K+/H+-ATPase measured in the presence of 5 mM KCl with an IC50 value of 1.3 microM. Kinetic studies indicated a competitive inhibition of ATPase by SCH 28080 with respect to K+. Studies on Na+/K+-ATPase showed that this enzyme was only slightly depressed by SCH 28080. It is concluded that SCH 28080 acts with high selectivity on the parietal cell K%/H+-ATPase, establishing its antisecretory effect by a competitive interaction with the high affinity K+-site of the gastric ATPase.
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Definition and Antagonism of Histamine H2-receptors
J. W. Black, W. A. M. Duncan, C. J. DURANT et al. · Nature · 1972 · 2.3K citations
A nonelectrogenic H+ pump in plasma membranes of hog stomach.
George Sachs, H. H. Chang, E. Rabon et al. · Journal of Biological Chemistry · 1976 · 602 citations · Full text