Environmental and Molecular Mutagenesis - Legacy Tobacco ...
Environmental and Molecular Mutagenesis - Legacy Tobacco ...
Environmental and Molecular Mutagenesis - Legacy Tobacco ...
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1989 EMS Abstracts<br />
S . typhimurium TA98 <strong>and</strong> TA100, with <strong>and</strong> without metabolic activation . The samples from Notes<br />
the Katsura showed the highest mutagenic activity (3500 revertants with TA98, . +59 ; 87<br />
revertants with TA9B, -S9~ 141 revertants with TA100, +S9 ; negative with TA100, -S9,<br />
per 0 .1-g equivalent of'bIue rayon) . By further measurement at several different sites<br />
of this river, we found that the effluent from a waste-water treatment plant in Kyoto<br />
City is the possible source of the mutagenic pollution . When the samples collected<br />
from this river in the winter <strong>and</strong> summer of 1988 were fractionated by TLC, the mutagenic<br />
activity in TA98 with metabolic activation was found predominantly in single identical<br />
zones . It is suggested that River Katsura is constantly polluted with certain<br />
frameshift promutagens of polycyclic structures .<br />
490<br />
SALMONELLA MUTAGENICITY TEST ON VARIOUS KIND OF IRRADIATED SUGARS AND AMIlIO ACIDS<br />
K . Sakamoto, K . Kanazashi, S . Iwahara, K .Takatori, <strong>and</strong> R . Aibara, Hatano Research<br />
Institute, Food <strong>and</strong> Drug Safety Center, Hadano, [anagawa (Japan)<br />
Recently, various kind of irradiated foods were studied in mutagenicity tests .<br />
Every food comprises variety of components, but the volume of samples that can be<br />
used by these test systems is limited . Accordingly, even if certain components of<br />
the irradiated food should undergo mutagenic changes, it would be impossible to<br />
detect such changes if the volume of them are smaller than the detectable limit of<br />
the test systems .<br />
For this reason, it is necessary to study mutagenicity on each irradiated food<br />
components . And if the test results indicate the formation of mutagens in component<br />
by irradiation, we should evaluate the genetic toxicity of irradiated foods with the<br />
test results in due consideration of : 1) irradiation dose, 2) ratio of mutagenic<br />
products formed from the irradiated food components, 3) strength of mutagenic<br />
activity, 4) proportion of components in food changeable to mutagens <strong>and</strong> 5) possibility<br />
of elimination of the mutagenic products .<br />
We studied Salmonella/mammalian microsome mutagenicity test on various kinds ofsugars<br />
<strong>and</strong> amino acids irradiated in the dry condition <strong>and</strong> in liquid solution with<br />
gamma ray of maximum dosage upto 10 kGy . As a result, weak mutagenic activity was<br />
detected in the 5% solution of cystein <strong>and</strong> 10% solution of arabinose irradilted at<br />
the maximum dosage of 10 kGy, with metabolic activation system . The results indicate<br />
that the mutagenic products from each compound hardly forms in irradiated foods .<br />
491<br />
CLASTOGENIC EFFECT OF ELLIPTICINE ON DIFFERENT PHASES OF THE CELL CYCLE OF<br />
CULTURED HUMAN LYMPHOCYTES AND ITS SYNERGISTIC ACTION WITH INHIBITORSOF<br />
DNA REPAIR AT G2 . Elza T . Sakamoto-Hojo <strong>and</strong> Catarina S . Takahashi'(IBILCE-<br />
S . Jose Rio PreEo-UNESP <strong>and</strong> FFCL de Ribeir`ao Preto-USP, BRASIL) .<br />
Ellipticine, a pyridocarbazole alkaloid, has shown an antitumor effect<br />
on several types of experimental <strong>and</strong> human tumors, being an intercalating<br />
substance whose mutagenicity has been demonstrated in several systems .<br />
To characterize the mechanism of action of this compound at the cell cycle<br />
level, human lymphocyte cultures from 2 healthy donors were treated with<br />
3 pg/ml ellipticine in 30-minute pulses during different phases of the<br />
cycle <strong>and</strong> analyzed for chromosome aberrations <strong>and</strong> sister chromatid exchanges<br />
. The G2 phase was more sensitive in terms of induction of aberrations,<br />
followed by S <strong>and</strong> G1 . The 24-h treatment (S phase) induced a four<br />
fold increase compared to th8 control . SCE induction was significant only<br />
at G1, when SCE frequency doubled_3The effect of lymphocytg post-treatment<br />
with inhibitors of DNA repair (10 M caffeine <strong>and</strong> 5 x 10 M 1-B-D-arabino<br />
furanosylcytosine) was also tested by adding 3 yg/ml ellipticine at G in<br />
30-minute pulses <strong>and</strong> the inhibitors immediately afterward during the2last<br />
3 h before harvesting the cultures . In the two experiments performed on<br />
blood from the 2 donors there was a moderate effect of chromosome aberration<br />
potentiation (about 2-3 times), i .e ., ellipticine bad a synergistic<br />
effect with both inhibitors in terms of chromosome aberration induction .<br />
492<br />
THE ABSENCE OF PAH HYDROXYLATION ACTIVITY IN TOBACCO CALLUS S9 . M . F . Salamone',<br />
S . Richard', C . J . Gentile', J . M . Gentiles, <strong>and</strong> D . A . Rokosh', 'Ministry of the<br />
Environment, Toronto, Canada <strong>and</strong> *Hope College, Holl<strong>and</strong>, Michigan .<br />
Microsomal enzymes (S9) from four week old photosynthetic <strong>and</strong> nonphotosynthetic<br />
tobacco (Nicotiana tobacum) callus cultures were prepared by two separate laboratories .<br />
The ability of each callus S9 to activate 2-aminofluorene (2AF) <strong>and</strong> benzo(a)pyrene<br />
(BaP) was then tested with the Ames fluctuation <strong>and</strong> plate incorporation assays . With<br />
each assay the callus S9 preparations from both laboratories increased the mutagenic<br />
http://legacy.library.ucsf.edu/tid/clb93d00/pdf<br />
.<br />
169<br />
Y