Environmental and Molecular Mutagenesis - Legacy Tobacco ...
Environmental and Molecular Mutagenesis - Legacy Tobacco ...
Environmental and Molecular Mutagenesis - Legacy Tobacco ...
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24 1989 EMS Abstracts 6 2<br />
http://legacy.library.ucsf.edu/tid/clb93d00/pdf<br />
Notes THE AUGER ELEGTRON DOSIMETRY OF INDIUM IN THE NUCLEUS OF V79 CELLS . D.H .<br />
Blakey', J.R. McLean', G .R. Douglas', D . Wilkinson', <strong>and</strong> J.M . Bayley', '<strong>Mutagenesis</strong> Section, Bureau of<br />
Chemical Hazards, <strong>and</strong> 'RadioPharmaceuticals Section, Bureau of Medical Devices, Department of National<br />
Health <strong>and</strong> Welfare, Ottawa, Canada, K1A 0I2.<br />
Many radiopharmaceuticals or their metabolites distribute to intracellular sites where the release of Auger<br />
electrons can damage radiosensitive structures such as DNA . The effect of intracellular "'udium eadne on<br />
chromosomal aberrations <strong>and</strong> cell killing was defined in terms of equivalent "Cobalt doses . About 30% of<br />
cell-associated "'In oxine was found in the nucleus <strong>and</strong> 7 .5% in the DNA. Based on the assumption that<br />
these effects result only from radioactivity in the cell nucleus, the radiation dose to a cell was estimated by<br />
chromosomal aberration analysis to be 9 .6 x 10' Gy/decay <strong>and</strong>, by the colony assay for cell survival to be<br />
10.1 x 10' Gy/decay. The dose based on chromosomal aberrations is probably underestimated, since data<br />
from cells with pulverized chromosomes were excluded from the calculations . Furthermore, the cellular<br />
radiation dose could be as high as 13 .0 x 10' Gy/decay if only the DNA-associated radioactivity was presumed<br />
to contribute to the biological endpoint . Using the method deaeribedby NCRP (Public . 63), the average<br />
radiation dose to the cell nucleus from introcxllular "'In was estimated to be about 3.3 x 10' Gy/decay.<br />
Accordingly, based on the biological dose estimates in this study, the relative biological effectiveness (RBE)<br />
for intracellular "'In was estimated to be as high as 3.1 (i.e. 10.1/3.3). Moreover, if the DNA-associated<br />
radioactivity is assumed to be the sole contributor to cellular damage, the RBE could be even higher .<br />
Virtually all of the energy absorbed in the nucleus would be from the nuclear-associated Auger electron, since<br />
thepe netrating emissions (x- <strong>and</strong> gamma rays, <strong>and</strong> internal conversion electrons) ~ntn'bute only 6 .1 x 1001<br />
Gy/decay. It would, therefore, appear that the conventional method of organ dosimetry, which presumes a<br />
uniform distribution of energy throughout the target volume, is inappropriate when applied to intracellular<br />
Auger electron emitting compounds such as "'In .<br />
NUTAGENICITY AND ANTIMDTACENICITY TESTING OF SIX CHEMICALS ASSOCIATED WITH<br />
THE PUNGENT PROPERTIES OF SPECIFIC SPICES. E. D. Elevins <strong>and</strong> Asliyati Asian,<br />
School of Public 6 Allied Health, Dept. of Health Sciencea, East Tennessee State<br />
Univeraity, Johnson City, Tli 37614.<br />
Six compounds, capsaiein, thymol, borneol . <strong>and</strong> allyl were screened for<br />
mutagenic activity using Salmonella t~hiauriom strains TA97, TA98 <strong>and</strong> TA100,<br />
with <strong>and</strong> without 89 metabolic activation. A11 six oompounds are associated with<br />
the pungent properties of some specific spices . It was observed that capsaicin<br />
was mutagenic using strain TA100 in the presence of 89. Capaaiein, found in the<br />
spice Cansicum annum, was detected <strong>and</strong> quantified using thin layer <strong>and</strong> gas<br />
chrosutographic techniques . The presence of an antimutagenic factor(s) in C.<br />
annum that could suppress the nutagenicity of capsaicin was detected. When the<br />
mutagens capsaicin <strong>and</strong> 2-aminoanthracene were assayed in the presence of C .<br />
annum acetone extract, using strain TA100 with 89 metabolic activation, the<br />
nutagenic response of both the mutagens were reduced by approxisutely 50%.<br />
Assaying capsaicin <strong>and</strong> 2-aminoanthracene in the presence of chlorophyll, the<br />
mutagenic response of the two smtagene were reduced by less than 401 . From this<br />
observation it was inferred that chloropbyll can successfully suppress the<br />
mutagenicity activities of capsaicin <strong>and</strong> 2-astinoanthracene, together with other<br />
antimutagenic factors that were present in the acetone extract of C. annum.<br />
THE DETECTION OF 1WTAGENECITY OF CKMfICAL FACTCRS IN INDUSTRY<br />
N. P.Boabko v<br />
Institute of Medical (ienetios ASS USSR, Mosco w<br />
The paper generalizes the results of the control of mutagenio effect<br />
of chemioals in real industry conditions (some plants) in the USSR . To<br />
detect possible mutageneoity danger of industry chemicals for a man oytogenetio<br />
analysis was made regarding the oooupational group of workers<br />
being in contact with chloroprene lead,dioetbyl phtalat dimethyl aoetamide,benao(a)<br />
pyrene,trichlorfon,d~methyl sulplute formaidelyde,ethylene<br />
ozide,vinyl chloride <strong>and</strong> also rubber industry wor>