Inhibitory Activity of α-Amylase and α-Glucosidase by Plant Extracts from the Brazilian Cerrado

被引:69
作者
de Souza, Paula Monteiro [1 ,2 ]
de Sales, Paloma Michelle [1 ]
Simeoni, Luiz Alberto [1 ]
Silva, Elton Clementino
Silveira, Damaris [1 ]
Magalhaes, Perola de Oliveira [1 ]
机构
[1] Univ Brasilia, Dept Pharmaceut Sci, Sch Hlth Sci, BR-70919970 Brasilia, DF, Brazil
[2] Univ Brasilia, Dept Farm, Fac Ciencias Saude, BR-70919970 Brasilia, DF, Brazil
关键词
enzyme inhibition; alpha-amylase; alpha-glucosidase; cerrado; Brazilian savannah; diabetes; ORAL ANTIHYPERGLYCEMIC THERAPY; IN-VITRO; QUALEA-GRANDIFLORA; EUGENIA; DERIVATIZATION; HYPERGLYCEMIA; HERB; ACID;
D O I
10.1055/s-0031-1280404
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Diabetes mellitus is the most common disease in the world. One therapeutic approach for treating diabetes is inhibition of alpha-amylase and alpha-glucosidase activities to reduce postprandial blood glucose levels. In vitro tests showed that several plant extracts from Brazilian cerrado species can inhibit the activity of alpha-amylase and alpha-glucosidase. The extracts of Eugenia dysenterica, Stryphnodendron adstringens, Pouteria caimito, Pouteria ramiflora, and Pouteria torta showed strong alpha-amylase and alpha-glucosidase inhibitory activity. Eugenia dysenterica, P. caimito, P. ramiflora, and P. torta aqueous extracts exerted the highest activity against alpha-amylase (IC50 values of 14.93, 13.6, 7.08, and 5.67 mu g/mL, respectively) and alpha-glucosidase (IC50 values of 0.46, 2.58, 0.35, and 0.22 mu g/mL, respectively). Stryphnodendron adstringens ethanol extract also exhibited inhibitory activity against both enzymes (IC50 1.86 mu g/mL against alpha-amylase and 0.61 mu g/mL against alpha-glucosidase). The results suggest that the activity of these cerrado plants on alpha-amylase and alpha-glucosidase represents a potential tool for development of new strategies for treatment of diabetes.
引用
收藏
页码:393 / 399
页数:7
相关论文
共 47 条
[21]   Medicinal plants of India with anti-diabetic potential [J].
Grover, JK ;
Yadav, S ;
Vats, V .
JOURNAL OF ETHNOPHARMACOLOGY, 2002, 81 (01) :81-100
[22]   Novel α-glucosidase inhibitors from Macaranga tanarius leaves [J].
Gunawan-Puteri, Maria D. P. T. ;
Kawabata, Jun .
FOOD CHEMISTRY, 2010, 123 (02) :384-389
[23]   Inhibition of human salivary α-amylase by glucopyranosylidene-spiro-thiohydantoin [J].
Gyémánt, G ;
Kandra, L ;
Nagy, V ;
Somsák, L .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2003, 312 (02) :334-339
[24]   Qualea grandiflora, a Brazilian "Cerrado" medicinal plant presents an important antiulcer activity [J].
Hiruma-Lima, CA ;
Santos, LC ;
Kushima, H ;
Pellizzon, CH ;
Silveira, GG ;
Vasconcelos, PCP ;
Vilegas, W ;
Brito, ARMS .
JOURNAL OF ETHNOPHARMACOLOGY, 2006, 104 (1-2) :207-214
[25]   Uses and abuses of in vitro tests in ethnopharmacology: Visualizing an elephant [J].
Houghton, P. J. ;
Howes, M.-J. ;
Lee, C. C. ;
Steventon, G. .
JOURNAL OF ETHNOPHARMACOLOGY, 2007, 110 (03) :391-400
[26]   DEOXYNOJIRIMYCIN - SYNTHESIS AND BIOLOGICAL-ACTIVITY [J].
HUGHES, AB ;
RUDGE, AJ .
NATURAL PRODUCT REPORTS, 1994, 11 (02) :135-162
[27]   Oral antihyperglycemic therapy for type 2 diabetes - Scientific review [J].
Inzucchi, SE .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2002, 287 (03) :360-372
[28]   α-Glucosidase inhibitors from Devil tree (Alstonia scholaris) [J].
Jong-Anurakkun, Nilubon ;
Bhandari, Megh Raj ;
Kawabata, Jun .
FOOD CHEMISTRY, 2007, 103 (04) :1319-1323
[29]   Inhibitory effects of tannin on human salivary α-amylase [J].
Kandra, L ;
Gyémánt, G ;
Zajácz, A ;
Batta, G .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2004, 319 (04) :1265-1271
[30]  
Karthic K, 2008, INDIAN J EXP BIOL, V46, P677