Am. Khalil, GENOTOXICITY OF 2 PHARMACOLOGICALLY IMPORTANT SELENIUM-COMPOUNDS (SELENOCYSTINE AND SELENOPURIDINE) IN CULTURED HUMAN BLOOD-LYMPHOCYTES, Toxicological and environmental chemistry, 41(3-4), 1994, pp. 147-154
Studies were conducted in vitro with human peripheral blood lymphocyte
s (72 h whole blood cultures) to determine the genotoxicity and cytoto
xicity of organic selenium compounds. Selenopuridine and selenocystine
at 1.05 x 10(-5) and 1.05 x 10(-4) M added for 48 h, significantly in
creased the percentage of aberrant cells. In addition, a trend towards
concentration-dependent increases in SCE was observed. These increase
s were statistically significant at high doses of selenium. Cytokineti
c analysis using cell proliferation and mitotic indices indicated that
selenium treatment resulted in mitotic delay, while has no significan
t effects on cell proliferation, under the conditions of our experimen
ts. These findings are discussed in terms of inhibitory effects of hig
h doses of organic forms of selenium on the growth of several biologic
al systems.