In vivo antiulcer activity, phytochemical exploration, and molecular modelling of the polyphenolic-rich fraction of Crepis sancta extract.
Animals
Anti-Ulcer Agents
/ pharmacology
Crepis
/ chemistry
Gastric Mucosa
/ drug effects
Male
Omeprazole
/ pharmacology
Phytochemicals
/ pharmacology
Phytotherapy
/ methods
Plant Extracts
/ pharmacology
Polyphenols
/ pharmacology
Pyrroles
/ pharmacology
Rats
Rats, Wistar
Stomach Ulcer
/ drug therapy
Sulfonamides
/ pharmacology
Antiulcer
AutoDock vina
Crepis sancta
Eudesmane sesquiterpenes
Molecular modelling
Polyphenolics
Journal
Inflammopharmacology
ISSN: 1568-5608
Titre abrégé: Inflammopharmacology
Pays: Switzerland
ID NLM: 9112626
Informations de publication
Date de publication:
Feb 2020
Feb 2020
Historique:
received:
17
06
2019
accepted:
20
08
2019
pubmed:
5
9
2019
medline:
18
11
2020
entrez:
5
9
2019
Statut:
ppublish
Résumé
Bioactivity-guided investigation of the methanol extract of Crepis sancta aerial parts, collected off Al-Tafilah, South Jordan, was applied, and in this study, the extract was explored for its phytochemical components and in vivo antiulcer activity. In addition, a docking study involving the purified compounds with the newly crystalized gastric proton pump (PDB # 5YLU) was performed. In-depth phytochemical investigation using the state-of-the-art chromatographic and analytical techniques was implemented resulting in the identification of two eudesmane-type sesquiterpenoids, 3-oxo-γ-costic acid (1) and its methyl ester (2) together with seven different methoxylated flavonols (3-9) as the extract's major components. The in vivo antiulcer study at three different doses (50, 100, and 200 mg/kg) against ethanol-induced gastric ulcer in male albino rats, compared to omeprazole (20 mg/kg) as a standard proton pump inhibitor antiulcer drug, revealed that the tested extract, at the middle and the highest doses, featured comparable or even superior activities relative to omeprazole as deduced from histopathological examination, in particular with regard to reducing inflammatory cell infiltration and ceasing mucosal haemorrhage. The tested extract revealed also a dose-dependent reduction in the volume and titrable acidity of the gastric juice together with a dose-dependent increase in the protective gastric mucin content which may explain the noticeable gastroprotective effect. Molecular modelling study of the isolated compounds showed a binding mode similar to the co-crystallized substrate vonoprazan in 5YLU which strengthens the importance of the tested extract as a potential natural remedy for treating gastric ulcer.
Identifiants
pubmed: 31482260
doi: 10.1007/s10787-019-00637-x
pii: 10.1007/s10787-019-00637-x
doi:
Substances chimiques
1-(5-(2-fluorophenyl)-1-(pyridin-3-ylsulfonyl)-1H-pyrrol-3-yl)-N-methylmethanamine
0
Anti-Ulcer Agents
0
Phytochemicals
0
Plant Extracts
0
Polyphenols
0
Pyrroles
0
Sulfonamides
0
Omeprazole
KG60484QX9
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
321-331Références
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