α-Glucosidase inhibition, 15-lipoxygenase inhibition, and brine shrimp toxicity of extracts and isolated compounds from Terminalia macroptera leaves

被引:31
作者
Anh Thu Pham [1 ]
Malterud, Karl Egil [1 ]
Paulsen, Berit Smestad [1 ]
Diallo, Drissa [2 ]
Wangensteen, Helle [1 ]
机构
[1] Univ Oslo, Sch Pharm, Sect Pharmaceut Chem, N-0316 Oslo, Norway
[2] Dept Tradit Med, Bamako, Mali
关键词
Chebulagic acid; corilagin; diabetes; flavonoids; polyphenols; tannins; LIPOXYGENASE; CONSTITUENTS; FRUITS;
D O I
10.3109/13880209.2014.880486
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Context: Terminalia macroptera Guill. & Perr. (Combretaceae), a tree that grows in West Africa, has been used in traditional medicine against a variety of diseases such as hepatitis, gonorrhea, skin diseases, and diabetes. Objective: To investigate enzyme inhibitory activity against a-glucosidase and 15-lipoxygenase (15-LO) and toxicity against brine shrimp of extracts and compounds from T. macroptera leaves. Materials and methods: Methanol extract, ethyl acetate, and butanol extracts obtained from the methanol extract, six isolated polyphenols (chebulagic acid, chebulic acid trimethyl ester, corilagin, methyl gallate, narcissin, and rutin), and shikimic acid were evaluated for enzyme inhibition and toxicity. Results: In enzyme inhibition assays, all extracts showed high or very high activity. Chebulagic acid showed an IC50 value of 0.05 mu M towards alpha-glucosidase and 24.9 +/- 0.4 mu M towards 15-LO, in contrast to positive controls (acarbose: IC50 201 +/- 28 mu M towards alpha-glucosidase, quercetin: 93 +/- 3 mu M towards 15-LO). Corilagin and narcissin were good 15-LO and alpha-glucosidase inhibitors, as well, while shikimic acid, methyl gallate, and chebulic acid trimethyl ester were less active or inactive. Rutin was a good alpha-glucosidase inhibitor (IC50 ca. 3 mu M), but less active towards 15-LO. None of the extracts or the isolated compounds seemed to be very toxic in the brine shrimp assay compared with the positive control podophyllotoxin. Conclusion: Inhibition of a-glucosidase in the gastrointestinal tract may be a rationale for the medicinal use of T. macroptera leaves against diabetes in traditional medicine in Mali. The plant extracts and its constituents show strong inhibition of the peroxidative enzyme 15-LO.
引用
收藏
页码:1166 / 1169
页数:4
相关论文
共 21 条
[11]  
Ha DoThi Ha DoThi, 2010, Natural Product Sciences, V16, P68
[12]  
Kubo I., 2010, OPEN BIOACT COMPD J, V3, P1, DOI [10.2174/1874847301003010001, DOI 10.2174/1874847301003010001]
[13]   In vitro survey of alpha-glucosidase inhibitory food components [J].
Matsui, T ;
Yoshimoto, C ;
Osajima, K ;
Oki, T ;
Osajima, Y .
BIOSCIENCE BIOTECHNOLOGY AND BIOCHEMISTRY, 1996, 60 (12) :2019-2022
[14]  
ROBAK J, 1988, POL J PHARMACOL PHAR, V40, P451
[15]   Design and synthesis of 4-methoxyphenylacetic acid esters as 15-lipoxygenase inhibitors and SAR comparative studies of them [J].
Sadeghian, Hamid ;
Attaran, Neda ;
Jafari, Zeinab ;
Saberi, Mohammad Reza ;
Pordel, Mehdi ;
Riazi, Mohammad Mahdi .
BIOORGANIC & MEDICINAL CHEMISTRY, 2009, 17 (06) :2327-2335
[16]   Lipoxygenase inhibitors from natural plant sources. Part 1: Medicinal plants with inhibitory activity on arachidonate 5-lipoxygenase and 5-lipoxygenase/cyclooxygenase [J].
Schneider, I ;
Bucar, F .
PHYTOTHERAPY RESEARCH, 2005, 19 (02) :81-102
[17]   Antioxidant constituents in the dayflower (Commelina communis L.) and their α-glucosidase-inhibitory activity [J].
Shibano, Makio ;
Kakutani, Koji ;
Taniguchi, Masahiko ;
Yasuda, Masahide ;
Baba, Kimiye .
JOURNAL OF NATURAL MEDICINES, 2008, 62 (03) :349-353
[18]   A MICROWELL CYTOTOXICITY ASSAY USING ARTEMIA-SALINA (BRINE SHRIMP) [J].
SOLIS, PN ;
WRIGHT, CW ;
ANDERSON, MM ;
GUPTA, MP ;
PHILLIPSON, JD .
PLANTA MEDICA, 1993, 59 (03) :250-252
[19]   Maplexins, new α-glucosidase inhibitors from red maple (Acer rubrum) stems [J].
Wan, Chunpeng ;
Yuan, Tao ;
Li, Liya ;
Kandhi, Vamsikrishna ;
Cech, Nadja B. ;
Xie, Mingyong ;
Seeram, Navindra P. .
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2012, 22 (01) :597-600
[20]   Antioxidant activity in extracts from coriander [J].
Wangensteen, H ;
Samuelsen, AB ;
Malterud, KE .
FOOD CHEMISTRY, 2004, 88 (02) :293-297