Changes in liver nuclear protein metabolism after a single dose of urethane to suckling mice

• Published in: Chemico-biological interactions Vol. 19; no. 3; p. 327
• Main Authors: Gronow, M, Lewis, F A
• Format: Journal Article
• Language: English
• Published: Ireland 01.12.1977
• Subjects: Animals; Animals, Newborn; Carcinogens - pharmacology; DNA - biosynthesis; Histones - biosynthesis; Liver - drug effects; Liver - metabolism; Mice; Nucleoproteins - biosynthesis; Time Factors; Tryptophan - metabolism; Urethane - pharmacology
• DOI: 10.1016/0009-2797(77)90055-2
• ISSN: 0009-2797

Treatment of 8-9-day-old C57BL/A mice with a single carcinogenic dose of urethane, at 1.2 mg/g body wt., resulted in an immediate decrease in liver DNA synthesis reaching a maximum at about 16-18 h after injection, the rate of synthesis returning to normal after 48 h. When the nuclear proteins were radiolabelled, the non-histone protein (NHP) fraction showed a significant decrease in specific activity 8-18 h after injection of urethane and slight increase in specific activity after 24 h. Histone and residual proteins did not show any significant change. The liver NHP were analysed by isoelectric focusing (IEF) and sodium dodecyl sulphate (SDS) electrophoresis in polyacrylamide gels. The latter technique failed to show any distinctive differences but IEF results indicated some quantitative and qualitative changes in protein content and synthesis were induced by the urethane treatment. The most noticeable change in the stained gels was an increase in a protein component having a pI of 7.35 and the appearance of new bands at pI's of 7.85 and 5.55 in the 18 h treated livers. However, the [3H]tryptophan labelling pattern indicated that this was not due to an increased synthesis of these components. 24 h after urethane there appeared to be an increased rate of synthesis of some of the major components of the mixture, particularly at the pI 5.65 region. Histone and residual protein fractions were also analysed by electrophoresis and showed no difference between treated and control livers.