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In vivo inhibition of gastric acid secretion by the aqueous extract of Scoparia dulcis L. in rodents
Authors:Mesía-Vela Sonia  Bielavsky Monica  Torres Luce Maria Brandão  Freire Sonia Maria  Lima-Landman Maria Teresa R  Souccar Caden  Lapa Antonio José
Affiliation:1. Natural Products Section, Department of Pharmacology, Escola Paulista de Medicina, Universidade Federal de São Paulo, 04044-020 Rua 03 de Maio 100, São Paulo, SP, Brazil;2. Centro de Ciencias Biologicas e da Saude, Universidade Federal do Maranhao, MA, Brazil
Abstract:The freeze-dried aqueous extract (AE) from the aerial parts of Scoparia dulcis was tested for its effects on experimental gastric hypersecretion and ulcer in rodents. Administration of AE to animals with 4h pylorus ligature potently reduced the gastric secretion with ED(50)s of 195 mg/kg (rats) and 306 mg/kg (mice). The AE also inhibited the histamine- or bethanechol-stimulated gastric secretion in pylorus-ligated mice with similar potency suggesting inhibition of the proton pump. Bio-guided purification of the AE yielded a flavonoid-rich fraction (BuF), with a specific activity 4-8 times higher than the AE in the pylorus ligature model. BuF also inhibited the hydrolysis of ATP by H(+),K(+)-ATPase with an IC(50) of 500 microg/ml, indicating that the inhibition of gastric acid secretion of Scoparia dulcis is related to the inhibition of the proton pump. Furthermore, the AE inhibited the establishment of acute gastric lesions induced in rats by indomethacin (ED(50)=313 mg/kg, p.o.) and ethanol (ED(50)=490 mg/kg, p.o.). No influence of the AE on gastrointestinal transit allowed discarding a possible CNS or a cholinergic interaction in the inhibition of gastric secretion by the AE. Collectively, the present data pharmacologically validates the popular use of Scoparia dulcis in gastric disturbances.
Keywords:Scoparia dulcis   Scrophulariaceae   Antiacid   Medicinal plant   H+,K+-ATPase   Antiulcer
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