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Molecular Pharmacology, Vol 14, 1148-1155, Copyright © 1978 by the American Society for Pharmacology and Experimental Therapeutics
1 Department of Biochemistry, University of Freiburg, D-7800 Freiburg, Hermann-Herder-Str. 7, Germany
After the administration of actinomycin D,
-amanitin and D-galactosamine, the [3H]-leucine incorporation into total rat liver proteins and into nonhistone chromosomal
proteins decreased to about 50% and 20% of controls, respectively. At a low dose of
cycloheximide the [3H]leucine incorporation into nonhistone chromosomal proteins was
unaffected, while the incorporation into total liver proteins was decreased to 35% of
controls. The nonhistone chromosomal protein to DNA ratios changed to 94%, 78%, 149%
and 66% of the controls after actinomycin D,
-amanitin, cycloheximide and D-galactosamine, respectively. SDS-polyacrylamide gel electrophoresis showed different changes in
the nonhistone chromosomal protein patterns after the administration of actinomycin D,
-amanitin, cycloheximide and D-galactosamine. The findings are discussed with respect
to possible mechanisms involved in liver cell death.