Vitexin and isovitexin from the Leaves of Ficus deltoidea with in-vivo α-glucosidase inhibition
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作者:
Choo, C. Y.
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Univ Teknol MARA, Fac Pharm, MedChem Herbal Res Grp, Puncak Alam 42300, Selangor, MalaysiaUniv Teknol MARA, Fac Pharm, MedChem Herbal Res Grp, Puncak Alam 42300, Selangor, Malaysia
Choo, C. Y.
[1
]
Sulong, N. Y.
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Univ Teknol MARA, Fac Pharm, MedChem Herbal Res Grp, Puncak Alam 42300, Selangor, MalaysiaUniv Teknol MARA, Fac Pharm, MedChem Herbal Res Grp, Puncak Alam 42300, Selangor, Malaysia
Sulong, N. Y.
[1
]
Man, F.
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Univ Teknol MARA, Fac Pharm, MedChem Herbal Res Grp, Puncak Alam 42300, Selangor, MalaysiaUniv Teknol MARA, Fac Pharm, MedChem Herbal Res Grp, Puncak Alam 42300, Selangor, Malaysia
Man, F.
[1
]
Wong, T. W.
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Univ Teknol MARA, Nondestruct Biomed & Pharmaceut Res Ctr, Puncak Alam 42300, Selangor, MalaysiaUniv Teknol MARA, Fac Pharm, MedChem Herbal Res Grp, Puncak Alam 42300, Selangor, Malaysia
Wong, T. W.
[2
]
机构:
[1] Univ Teknol MARA, Fac Pharm, MedChem Herbal Res Grp, Puncak Alam 42300, Selangor, Malaysia
[2] Univ Teknol MARA, Nondestruct Biomed & Pharmaceut Res Ctr, Puncak Alam 42300, Selangor, Malaysia
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 alpha-glucosidase inhibition. Materials and Methods: The partitioned extracts, subtractions and pure bioactive constituents were subjected to alpha-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 alpha-glucosidase inhibition. (C) 2012 Elsevier Ireland Ltd. All rights reserved.
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页码:776 / 781
页数:6
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