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

被引:187
作者
Choo, C. Y. [1 ]
Sulong, N. Y. [1 ]
Man, F. [1 ]
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
关键词
Ficus deltoidea Jack; Moraceae; alpha-glucosidase inhibition; Acute toxicity; DIABETIC-RATS; EXTRACT; FLAVONOIDS; CONSTITUENTS;
D O I
10.1016/j.jep.2012.05.062
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
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.
引用
收藏
页码:776 / 781
页数:6
相关论文
共 32 条
  • [1] Adam Z., 2010, Research Journal of Medicinal Plant, V4, P61, DOI 10.3923/rjmp.2010.61.75
  • [2] Evaluation of the hypoglycemic effect of Cucurbita ficifolia Bouche, (Cucurbitaceae) in different experimental models
    Alarcon-Aguilar, FJ
    Hernandez-Galicia, E
    Campos-Sepulveda, AE
    Xolalpa-Molina, S
    Rivas-Vilchis, JF
    Vazquez-Carillo, LI
    Roman-Ramos, R
    [J]. JOURNAL OF ETHNOPHARMACOLOGY, 2002, 82 (2-3) : 185 - 189
  • [3] Acute toxicity studies of the leaf extract of Ficus exasperata on haematological parameters, body weight and body temperature
    Bafor, E. E.
    Igbinuwen, O.
    [J]. JOURNAL OF ETHNOPHARMACOLOGY, 2009, 123 (02) : 302 - 307
  • [4] Hypoglycemic effects of the wood of Taxus yunnanensis on streptozotocin-induced diabetic rats and its active components
    Banskota, AH
    Nguyen, NT
    Tezuka, Y
    Nobukawa, T
    Kadota, S
    [J]. PHYTOMEDICINE, 2006, 13 (1-2) : 109 - 114
  • [5] Acarbose-induced acute severe hepatotoxicity
    Carrascosa, M
    Pascual, F
    Aresti, S
    [J]. LANCET, 1997, 349 (9053) : 698 - 699
  • [6] Acarbose actions on insulin resistance and inflammatory parameters during an oral fat load
    Derosa, Giuseppe
    Maffioli, Pamela
    Ferrari, Ilaria
    Fogari, Elena
    D'Angelo, Angela
    Palumbo, Ilaria
    Randazzo, Sabrina
    Bianchi, Lucio
    Cicero, Arrigo F. G.
    [J]. EUROPEAN JOURNAL OF PHARMACOLOGY, 2011, 651 (1-3) : 240 - 250
  • [7] Dominguez E, 1996, PHYTOTHER RES, V10, P526, DOI 10.1002/(SICI)1099-1573(199609)10:6<526::AID-PTR886>3.0.CO
  • [8] 2-R
  • [9] Ganoderol B: A potent α-glucosidase inhibitor isolated from the fruiting body of Ganoderma lucidum
    Fatmawati, Sri
    Shimizu, Kuniyoshi
    Kondo, Ryuichiro
    [J]. PHYTOMEDICINE, 2011, 18 (12) : 1053 - 1055
  • [10] Bio-assay guided isolation and identification of α-glucosidase inhibitors from the leaves of Aquilaria sinensis
    Feng, Jie
    Yang, Xiu-Wei
    Wang, Ru-Feng
    [J]. PHYTOCHEMISTRY, 2011, 72 (2-3) : 242 - 247