Abstract

The frequency of chromosomal aberrations and cell lethality induced in synchronous CHO cells by X irradiation alone or X irradiation combined with a treatment of 0.05) or 1.5 M NaCl has been examined. Treatment with hypotonic 0.05 M NaCl increased the radiosensitivity, i.e., decreased the D/sub 0/ in M (D/sub 0/ from 87 to 61 rad), in G/sub 1/ (D/sub 0/ from 156 to 122 rad) and in S (D/sub 0/ from 165 to 128 rad). Exposure to hypertonic (1.5 M) NaCl decreased the radiosensitivity in G/sub 1/ and S; i.e., increased the D/sub 0/ in G/sub 1/ (D/sub 0/ from 156 to 182 rad) and in S (D/sub 0/ from 165 to 232 rad), while exposure to 1.5 M NaCl increased the radiosensitivity in mitosis (D/sub 0/ from 87 to 78 rad). The 0.05 or 1.5 M salt treatments had no observable effect on the radiation-induced division delay. The appearance of tetraploid cells following treatment of mitotic cells with 1.5 M NaCl indicates that the hypertonic treatment probably had a deleterious effect on the mitotic apparatus. Except for a decrease in the frequency of radiation-induced chromosomal aberrations in mitotic cells treated with 1.5 M NaCl, the changes in themore » frequency of chromosomal aberrations caused by the salt treatments correlated well with the changes in lethality delineated above. These positive correlations can be illustrated best by a plot of the logarithm of survival versus aberration frequency where the data points fell on a straight line havinga D tilde/sub 0/ of 0.8 aberration per cell. The salt-induced changes in cellular radiosensitivity are hypothesized to be caused by changes in the indirect effect of radiation, associated with free radicals produced in water and interacting in chromatin.« less

Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call