EFFECTS OF MONOSACCHARIDES AND DISACCHARIDES ON THE FORMATION OF FOOD MUTAGENS IN MODEL SYSTEMS

被引:89
作者
SKOG, K
JAGERSTAD, M
机构
[1] Food Chemistry, Chemical Center, University of Lund
来源
MUTATION RESEARCH | 1990年 / 230卷 / 02期
关键词
Ames test; Creatin(in)e; DiMeIQx; Food mutagens; Glycine; Hexoses; MeIQx; Model systems;
D O I
10.1016/0027-5107(90)90064-B
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The formation of the mutagenic imidazoquinoxalines (MeIQx, DiMeIQx) was studied using a modification of a previous model system. Creatine or creatinine (0.9 mmole) was heated together with glycine (0.9 mmole) and various sugars (0.45 mmole) dissolved in diethylene glycol and water (3 ml, 5 : 1) for up to 15 min at 180°C. This system produced the same amount of mutagenicity after 10 min at 180°C as a previous one during 2 h of reflux boiling at 12dgC. MeIQx (4 nmole/mmole creatin(in)e was the major mutagen produced together with minor amounts of DiMeIQx, both 4,8- and 7,8-DiMeIQx according to HPLC-MS. A few other mutagenic peaks were also separated on HPLC, but they were not identified. Varying the concentration (0-2.4 mmole) and type of monosaccharides and disaccharides greatly affected the yields of all the mutagenic compounds. Sugar in molar amounts lower than the creatin(in)e concentration increased the yield until an optimum was reached. In higher concentrations the formation of all the mutagens was markedly reduced. The same was found for glucose, fructose, sucrose, and lactose, though the monosaccharides showed the most pronounced inhibitory effects. The inhibition of the formation of the mutagenic compounds by an excess of sugars is proposed to be an effect of Maillard reaction products, which may block the formation of imidazoquinoxalines by attacking creatine. Support for this mechanism is given by data showing a lower recovery of unreacted creatine with increasing concentration of glucose and also by an inhibitory effect on the formation of these mutagens after adding a typical Maillard reaction product, 5-hydroxymethyl-2-furfural. © 1990.
引用
收藏
页码:263 / 272
页数:10
相关论文
共 27 条
[1]   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
[2]   ISOLATION AND IDENTIFICATION OF MUTAGENS FROM A FRIED NORWEGIAN MEAT PRODUCT [J].
BECHER, G ;
KNIZE, MG ;
NES, IF ;
FELTON, JS .
CARCINOGENESIS, 1988, 9 (02) :247-253
[3]   AN XAD-2 RESIN METHOD FOR EFFICIENT EXTRACTION OF MUTAGENS FROM FRIED GROUND-BEEF [J].
BJELDANES, LF ;
GROSE, KR ;
DAVIS, PH ;
STUERMER, DH ;
HEALY, SK ;
FELTON, JS .
MUTATION RESEARCH, 1982, 105 (1-2) :43-49
[4]   CHARACTERIZATION OF DEVELOPING OAT SEED MESSENGER-RNA - EVIDENCE FOR MANY GLOBULIN MESSENGER-RNAS [J].
FABIJANSKI, S ;
MATLASHEWSKI, GJ ;
ALTOSAAR, I .
PLANT MOLECULAR BIOLOGY, 1985, 4 (04) :205-210
[5]  
FELTON J, 1986, ENERGY TECHNOL REV, P1
[6]  
FELTON JS, 1988, CARCINOGENIC MUTAGEN, P73
[7]  
HAYATSU H, 1983, JPN J CANCER RES, V74, P472
[8]   FORMATION OF 2-AMINO-3,8-DIMETHYLIMIDAZO[4,5-F]QUINOXALINE IN A MODEL SYSTEM BY HEATING CREATININE, GLYCINE AND GLUCOSE [J].
JAGERSTAD, M ;
OLSSON, K ;
GRIVAS, S ;
NEGISHI, C ;
WAKABAYASHI, K ;
TSUDA, M ;
SATO, S ;
SUGIMURA, T .
MUTATION RESEARCH, 1984, 126 (03) :239-244
[9]  
JAGERSTAD M, 1983, ACS SYM SER, V215, P507
[10]  
JAGERSTAD M, 1989, IN PRESS 5TH P SAT S