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Inhibition of gastric H+, K+-ATPase by chalcone derivatives, xanthoangelol and 4-hydroxyderricin, from <i>Angelica keiskei</i> Koidzumi
50
Citations
10
References
1990
Year
Molecular PharmacologyMedicinal ChemistryInhibitory ActivityBiochemistryGastrointestinal PharmacologyMedicinePhysiologyNatural SciencesPhytochemistryPig Gastric H+PhytopharmacologyPharmacotherapyChalcone DerivativesMetabolismPharmacologyGastric H+Drug DiscoveryOxidative Stress
Two chalcone derivatives, xanthoangelol (1) and 4-hydroxyderricin (II) isolated from Angelica keiskei Koidzumi, inhibited pig gastric H+, K(+)-ATPase with IC50 values of 1.8 and 3.3 microM, respectively. The inhibition by I or II was competitive with respect to ATP and was non-competitive with respect to K+ I and II also inhibited K+, stimulated p-nitrophenyl phosphatase, with IC50 values of 1.3 and 3.5 microM, respectively. Proton transport in-vitro was inhibited by I or II, in a dose-dependent manner, 1 at 100 mg kg-1, i.p. significantly inhibited acid secretion and the formation of stress-induced gastric lesions. These results suggest that the antisecretory effect of 1 is due to the inhibition of gastric H+, K(+)-ATPase.
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