Genotoxicity of gardenia yellow and its components

被引:118
作者
Ozaki, A
Kitano, M
Furusawa, N
Yamaguchi, H
Kuroda, K
Endo, G
机构
[1] Osaka City Univ, Sch Med, Dept Prevent Med & Environm Hlth, Abeno Ku, Osaka 5458585, Japan
[2] Osaka City Inst Publ Hlth & Environm Sci, Tennoji Ku, Osaka 5430026, Japan
[3] Osaka City Univ, Fac Human Life Sci, Sumiyoshi Ku, Osaka 5588585, Japan
关键词
gardenia yellow; genipin; sister chromatid exchange; tetraploid; capillary electrophoresis;
D O I
10.1016/S0278-6915(02)00118-7
中图分类号
TS2 [食品工业];
学科分类号
0832 [食品科学与工程];
摘要
Gardenia fruit (Gardenia jasminoides ELLIS) is widely used as a natural food colorant and as a traditional Chinese medicine for treatment of hepatic and inflammatory diseases. "Gardenia yellow" is a natural food colorant which is extracted by ethanol from gardenia fruit. The purpose of this study was to evaluate the genotoxicity of gardenia yellow. Genotoxicity of gardenia yellow and its components, crocetin, gentiobiose (a component of crocin), geniposide and genipin (formed by hydrolysis of geniposide), was studied by Ames test, rec-assay, and sister chromatid exchange (SCE) using V79 cells. Gardenia yellow and its components were found not to be mutagenic in the Salmonella reverse mutation assay. Gardenia yellow and genipin caused damage of DNA in rec-assay. Gardenia yellow induced a significant dose-dependent increase of SCE frequency (8.6 times at 1000 mug/ml as the value for the solvent control). Only genipin induced SCEs significantly among the components of gardenia yellow. Moreover, genipin induced a significant increase of tetraploids at all doses tested (95% at 8 mug/ml). Gardenia yellow preparation was analyzed by capillary electrophoresis (CE), and geniposide was detected. However, genipin was not observed. In conclusion, we have shown that genipin possesses genotoxicity. Furthermore, there were unidentified genotoxicants in gardenia yellow. (C) 2002 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:1603 / 1610
页数:8
相关论文
共 32 条
[21]
NODA T, 1984, SEIKATSU EISEI, V28, P80
[22]
Mutagenicity and DNA-damaging activity of decomposed products of food colours under UV irradiation [J].
Ozaki, A ;
Kitano, M ;
Itoh, N ;
Kuroda, K ;
Furusawa, N ;
Masuda, T ;
Yamaguchi, H .
FOOD AND CHEMICAL TOXICOLOGY, 1998, 36 (9-10) :811-817
[23]
NEW GIEMSA METHOD FOR DIFFERENTIAL STAINING OF SISTER CHROMATIDS [J].
PERRY, P ;
WOLFF, S .
NATURE, 1974, 251 (5471) :156-158
[24]
CYTOLOGICAL DETECTION OF MUTAGEN CARCINOGEN EXPOSURE BY SISTER CHROMATID EXCHANGE [J].
PERRY, P ;
EVANS, HJ .
NATURE, 1975, 258 (5531) :121-125
[25]
PHARMACOLOGICAL STUDIES ON IRIDOID COMPOUNDS .2. RELATIONSHIP BETWEEN STRUCTURES AND CHOLERETIC ACTIONS OF IRIDOID COMPOUNDS [J].
TAKEDA, S ;
YUASA, K ;
ENDO, T ;
ABURADA, M .
JOURNAL OF PHARMACOBIO-DYNAMICS, 1980, 3 (10) :485-492
[26]
TOUYAMA R, 1994, CHEM PHARM BULL, V42, P1571
[27]
TOUYAMA R, 1994, CHEM PHARM BULL, V42, P668, DOI 10.1248/cpb.42.668
[28]
Tsai CC, 2000, J BIOMED MATER RES, V52, P58, DOI 10.1002/1097-4636(200010)52:1<58::AID-JBM8>3.0.CO
[29]
2-0
[30]
Yamada S, 1996, J FOOD HYG SOC JPN, V37, P372