Vitexin and isovitexin from the Leaves of Ficus deltoidea with in-vivo α-glucosidase inhibition

Ethnopharmacological relevance: The leaves of Ficus deltoidea are used as a traditional medicine by diabetes patients in Malaysia. Aim of the study: The objective of the study is to identify and evaluate bioactive constituents with in vivo α-glucosidase inhibition. Materials and Methods: The partiti...

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書目詳細資料
發表在:Journal of Ethnopharmacology
主要作者: 2-s2.0-84863985161
格式: Article
語言:English
出版: 2012
在線閱讀:https://www.scopus.com/inward/record.uri?eid=2-s2.0-84863985161&doi=10.1016%2fj.jep.2012.05.062&partnerID=40&md5=ce0eb29006e96da3dfcafa2bf3a0ddfd
實物特徵
總結:Ethnopharmacological relevance: The leaves of Ficus deltoidea are used as a traditional medicine by diabetes patients in Malaysia. Aim of the study: The objective of the study is to identify and evaluate bioactive constituents with in vivo α-glucosidase inhibition. Materials and Methods: The partitioned extracts, subfractions and pure bioactive constituents were subjected to α-glucosidase inhibition assay. The identified bioactive constituents were administered orally to sucrose loaded normoglycemic mice and induced diabetic rats. The postprandial blood glucose levels were monitored at 30 min interval. Acute toxicity was evaluated in both normoglycemic mice and induced diabetic rats. Results: Bioactivity guided fractionation led to the isolation of both vitexin (1) and isovitexin (2). Oral administration of 1 mg/kg of either vitexin (1) or isovitexin (2) significantly (p<0.05) reduced the postprandial blood glucose level in sucrose loaded normoglycemic mice at 30 min. The percentage of postprandial blood glucose reduction was highest in sucrose loaded induced diabetic rats administered orally with 200 mg/kg of vitexin (1) or 100 mg/kg of isovitexin (2). Both vitexin (1) and isovitexin (2) did not exert any signs of toxicity at the highest dose of 2 g/kg administered orally to normoglycemic mice and induced diabetic rats. Conclusion: Both the C-glycosyl bioflavonoids, namely, vitexin (1) and isovitexin (2) exhibited in vivo α-glucosidase inhibition. © 2012 Elsevier Ireland Ltd.
ISSN:18727573
DOI:10.1016/j.jep.2012.05.062