Genetic toxicity of a standardized mixture of citrus polymethoxylated flavones

被引:38
作者
Delaney, B
Phillips, K
Vasquez, C
Wilson, A
Cox, D
Wang, HB
Manthey, J
机构
[1] Cargill Hlth & Food Technol, Wayzata, MN 55391 USA
[2] Midwest Res Inst, Kansas City, MO 64110 USA
[3] Cargill Feed Applicat, Minneapolis, MN 55440 USA
[4] Cargill Citro Amer Inc, St Frostproof, FL 33843 USA
[5] ARS, USDA, SAA, US Citrus & Subtrop Prod Lab, Winter Haven, FL 33881 USA
关键词
polymethoxylated flavone; citrus; mutagenicity;
D O I
10.1016/S0278-6915(02)00007-8
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
Flavonoids are a ubiquitous family of phytochemicals that display a variety of biological effects. both beneficial and adverse depending on the individual compound. Certain flavonoids are genotoxic while others inhibit the genotoxicity of other mutagens. In the present studies. the mutagenicity of a mixture of polymethoxylated flavones (PMFs) purified from citrus peel oil was evaluated. The mixture consisted of nobiletin (32.5%), 3,3',4',5,6,7,8-heptamethoxyflavone (25.0%), tangeretin (14.0%). trimethylscutellarein (9.1%), sinensetin (3.9%), 5-demethyl-nobiletin (2.8%), hexa-O-methylquercetagetin (3.3%), 5-demethyl-tetramethylscutellarein (0.7%). 5-hydroxy-3,3'.4'.6,7,8-hexamethoxyflavone (0.7%), and a small quantity of unidentified flavonoid compounds (3.9%). In vitro addition of the PMF mixture over a concentration range that spanned four log doses (0.0005-5.0 mg/plate) did not reveal any evidence of mutagenicity in five bacterial tester strains (Salmonella typhimurium TA98, TA100, TA102, TA1535 and TA1537) either in the absence or presence of S9 activation. The PMF mixture exhibited a statistically significant increase in mutagenicity of L5178Y tk(+/-) mouse lymphoma cells at 0.05 (38.5x10(-6): P<0.05) and 0.1 mg/ml (61x10(-6): P<0.01) compared with vehicle-treated controls (mutation frequency = 19.7x10(-6)). However, these responses were within historical values observed in negative control cultures and extremely small compared to the positive control (EMS 0.5 mul/ml; 1685.3x10(-6)). Furthermore, in the presence of S9 there was no indication of genetic toxicity in L5178Y tk(+/-) cells. These results demonstrate that the PMF mixture is not genotoxic in in vitro assay systems. (C) 2002 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:617 / 624
页数:8
相关论文
共 44 条
[1]
Aeschbacher H U, 1982, Nutr Cancer, V4, P90, DOI 10.1080/01635588209513744
[2]
MODIFICATION OF INVIVO HETEROCYCLIC AMINE GENOTOXICITY BY DIETARY FLAVONOIDS [J].
ALLDRICK, AJ ;
LAKE, BG ;
ROWLAND, IR .
MUTAGENESIS, 1989, 4 (05) :365-370
[3]
METHODS FOR DETECTING CARCINOGENS AND MUTAGENS WITH SALMONELLA-MAMMALIAN-MICROSOME MUTAGENICITY TEST [J].
AMES, BN ;
MCCANN, J ;
YAMASAKI, E .
MUTATION RESEARCH, 1975, 31 (06) :347-363
[4]
ANTI-MUTAGENESIS AND ANTI-PROMOTION BY APIGENIN, ROBINETIN AND INDOLE-3-CARBINOL [J].
BIRT, DF ;
WALKER, B ;
TIBBELS, MG ;
BRESNICK, E .
CARCINOGENESIS, 1986, 7 (06) :959-963
[5]
THE FLAVONOID TANGERETIN INHIBITS INVASION OF MO4 MOUSE CELLS INTO EMBRYONIC CHICK HEART INVITRO [J].
BRACKE, ME ;
VYNCKE, BM ;
VANLAREBEKE, NA ;
BRUYNEEL, EA ;
DEBRUYNE, GK ;
DEPESTEL, GH ;
DECOSTER, WJ ;
ESPEEL, MF ;
MAREEL, MM .
CLINICAL & EXPERIMENTAL METASTASIS, 1989, 7 (03) :283-300
[6]
BUENING MK, 1981, CANCER RES, V41, P67
[7]
Inhibition of bacterial mutagenesis by Citrus flavonoids [J].
Calomme, M ;
Pieters, L ;
Vlietinck, A ;
VandenBerghe, D .
PLANTA MEDICA, 1996, 62 (03) :222-226
[8]
APIGENIN AND TANGERETIN ENHANCE GAP JUNCTIONAL INTERCELLULAR COMMUNICATION IN RAT-LIVER EPITHELIAL-CELLS [J].
CHAUMONTET, C ;
BEX, V ;
GAILLARDSANCHEZ, I ;
SEILLANHEBERDEN, C ;
SUSCHETET, M ;
MARTEL, P .
CARCINOGENESIS, 1994, 15 (10) :2325-2330
[9]
CREBELLI R, 1990, MICROBIOLOGICA, V13, P115
[10]
DAS M, 1987, CANCER RES, V47, P760