EVALUATING THE RELATIONSHIP OF METABOLIC-ACTIVATION SYSTEM CONCENTRATIONS AND CHEMICAL DOSE CONCENTRATIONS FOR THE SALMONELLA SPIRAL AND PLATE ASSAYS

被引:7
作者
CLAXTON, LD
HOUK, VS
ALLISON, JC
CREASON, J
机构
[1] Health Effects Research Laboratory, U.S. Environmental Protection Agency, Research Triangle Park
来源
MUTATION RESEARCH | 1991年 / 253卷 / 02期
关键词
PROMUTAGENS; SALMONELLA SPIRAL ASSAY; SPIRAL ASSAY; PLATE ASSAY; ACETYLAMINOFLUORENE; 2-AMINOANTHRACENE; BENZO[A]PYRENE;
D O I
10.1016/0165-1161(91)90126-S
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
A factorial experimental design was used within this study to evaluate the influence of multiple metabolic activation system concentrations on the dose-response exhibited by promutagens (indirect-acting mutagens) in the Salmonella spiral and plate assays. The mutagenic activity of the three compounds used spanned three orders of magnitude. The mutagenic activity of the compounds ranged from 10 to 100 revertants/mu-g for acetylaminofluorene (2AAF) to more than 1000 revertants/mu-g for 2-aminoanthracene (2AA). Benzo[a]pyrene (BaP) activity was within an intermediate range (100-1000 revertants/mu-g). During a single experiment, a mutagen was tested in TA100 at 13 doses plus a negative control dose. Each dose was tested at 10 S9 concentrations. The S9 concentrations ranged from 0.1 mg protein/plate to 4 mg protein/plate in the standard plate assay and from 0.25 to 4.90 mg-equivalents in the spiral assay. The spiral Salmonella assay, an automated version of the standard assay, generates dose-response data from a concentration gradient on a single agar plate, thereby providing a straightforward approach to this type of study. This study demonstrates not only that even small differences in S9 concentrations can affect the measurement of mutagenic potency but that S9/compound interactions cannot be generalized through the use of interaction studies. This study also shows that spiral assay data and plate assay data for promutagens cannot be compared directly unless the S9 concentrations for all chemical doses are also comparable.
引用
收藏
页码:127 / 136
页数:10
相关论文
共 23 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]   MUTAGENICITY OF THE FRACTIONATED ORGANIC EMISSIONS FROM DIESEL, CIGARETTE-SMOKE CONDENSATE, COKE-OVEN, AND ROOFING TAR IN THE AMES ASSAY [J].
AUSTIN, AC ;
CLAXTON, LD ;
LEWTAS, J .
ENVIRONMENTAL MUTAGENESIS, 1985, 7 (04) :471-487
[3]   THE SALMONELLA MAMMALIAN MICROSOME MUTAGENICITY TEST - COMPARISON OF HUMAN AND RAT LIVERS AS ACTIVATING SYSTEMS [J].
BEAUNE, P ;
LEMESTRECORNET, R ;
KREMERS, P ;
ALBERT, A ;
GIELEN, J .
MUTATION RESEARCH, 1985, 156 (03) :139-146
[5]   GUIDE FOR THE SALMONELLA-TYPHIMURIUM MAMMALIAN MICROSOME TESTS FOR BACTERIAL MUTAGENICITY [J].
CLAXTON, LD ;
ALLEN, J ;
AULETTA, A ;
MORTELMANS, K ;
NESTMANN, E ;
ZEIGER, E .
MUTATION RESEARCH, 1987, 189 (02) :83-91
[6]  
CLAXTON LD, 1991, MUTAT RES, V253, P149, DOI 10.1016/0165-1161(91)90128-U
[7]  
Graedel T. E., 1986, ATMOSPHERIC CHEM COM
[8]   SALMONELLA MUTAGENICITY TEST-RESULTS FOR 250 CHEMICALS [J].
HAWORTH, S ;
LAWLOR, T ;
MORTELMANS, K ;
SPECK, W ;
ZEIGER, E .
ENVIRONMENTAL MUTAGENESIS, 1983, 5 :3-&
[9]  
HOUK VS, 1989, MUTAT RES, V223, P49