Effect of five flavonoid compounds isolated from leaves of Diospyros kaki on stimulus-induced superoxide generation and tyrosyl phosphorylation of proteins in human neutrophils

被引:32
作者
Chen, G
Lu, HW
Wang, CL
Yamashita, K
Manabe, M
Meng, ZY
Xu, SX
Kodama, H [1 ]
机构
[1] Kochi Med Sch, Dept Chem, Nanko Ku, Kochi 7838505, Japan
[2] Kochi Med Sch, Dept Anesthesiol & Resusitol, Nanko Ku, Kochi 7838505, Japan
[3] Shenyang Pharmaceut Univ, Dept Phytochem, Shenyang 110015, Peoples R China
关键词
flavonoid; superoxide generation; tyrosyl phosphorylation; human neutrophils;
D O I
10.1016/S0009-8981(02)00298-X
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 [基础医学];
摘要
Background: The crude drug "kaki-yo" is a traditional medicine used in Japan as a hypotensive drug. Methods: The effect of five flavonoid compounds isolated from the leaves of Diospyros kaki was investigated on the stimulus-induced superoxide generation and phosphorylation of tyrosine residues of protein in human neutrophils. The five compounds examined were kaempferol 3-O-beta-D-galactopyranoside (TR), kaempferol 3-O-beta-D-glucopyranoside (AS), isorhamnetin 3-O-beta-D-glucopyranoside (IS), quercetin 3-O-beta-D-galactopyranoside (HY), quercetin 3-O-beta-D-glucopyranosyl-(6-->1)-alpha-L-rhamnopyranoside (RU). Results: When the cells were preincubated with these five compounds, the superoxide generation induced by N-formyl-methionyl-leucyl-phenylalanine (fMLP) was significantly suppressed in a concentration-dependent manner. The arachidonic acid (AA)-induced superoxide generation was suppressed by TR, AS, HY and RU. On the other hand, the superoxide generation was weakly enhanced by IS in low concentration (5-20 mumol/l), but was suppressed in high concentration (50 mumol/l). The superoxide generation induced by phorbol 12-myristate 13-acetate (PMA) suppressed the TR, IS, HY and RU, but AS gave no effect. When the cells were incubated with fMLP in the presence of TR, IS and RU, fMLP-induced tyrosyl phosphorylation of 45-kDa proteins of the cells was dose-dependently suppressed in parallel to the suppression of fMLP-induced superoxide generation. These five flavonoids showed almost no hemolytic effect even at a concentration of 500 mumol/l. Conclusion: Flavonoid compounds suppressed stimulus-induced superoxide generation and tyrosyl phosphorylation and may have pharmaceutical application. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:169 / 175
页数:7
相关论文
共 22 条
[1]
NADPH oxidase: An update [J].
Babior, BM .
BLOOD, 1999, 93 (05) :1464-1476
[2]
Flavonols, flavones and anthocyanins as native antioxidants of food and their possible role in the prevention of chronic diseases [Flavonole, flavone und anthocyane als naturliche antioxidantien der nahrung und ihre mogliche rolle bei der pravention chronischer erkrankungen] [J].
Böhm H. ;
Boeing H. ;
Hempel J. ;
Raab B. ;
Kroke A. .
European Journal of Nutrition, 1998, 37 (2) :147-163
[3]
CLARK RA, 1991, J INFECT DIS S2, V179, pS309
[4]
FUNAYAMA S, 1979, CHEM PHARM BULL, V27, P2865
[5]
JEANETTE HW, 1996, FRONT BIOSCI, V1, pD72
[6]
INHIBITORY EFFECTS OF VARIOUS FLAVONOIDS ISOLATED FROM LEAVES OF PERSIMMON ON ANGIOTENSIN-CONVERTING ENZYME-ACTIVITY [J].
KAMEDA, K ;
TAKAKU, T ;
OKUDA, H ;
KIMURA, Y ;
OKUDA, T ;
HATANO, T ;
AGATA, I ;
ARICHI, S .
JOURNAL OF NATURAL PRODUCTS, 1987, 50 (04) :680-683
[7]
Novel priming compounds of cystathionine metabolites on superoxide generation in human neutrophils [J].
Kodama, H ;
Zhang, JY ;
Sugahara, K .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2000, 269 (02) :297-301
[8]
CLEAVAGE OF STRUCTURAL PROTEINS DURING ASSEMBLY OF HEAD OF BACTERIOPHAGE-T4 [J].
LAEMMLI, UK .
NATURE, 1970, 227 (5259) :680-+
[9]
Effect of three flavonoids, 5,7,3′,4′-tetrahydroxy-3-methoxy flavone, luteolin, and quercetin, on the stimulus-induced superoxide generation and tyrosyl phosphorylation of proteins in human neutrophil [J].
Lu, HW ;
Sugahara, K ;
Sagara, Y ;
Masuoka, N ;
Asaka, Y ;
Manabe, M ;
Kodama, H .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 2001, 393 (01) :73-77
[10]
Pharmacology and chemotaxonomy of Diospyros [J].
Mallavadhani, UV ;
Panda, AK ;
Rao, YR .
PHYTOCHEMISTRY, 1998, 49 (04) :901-951