Comparison of acute hepatocellular proliferating cell nuclear antigen labeling indices and growth fractions, p34cdc2 kinases, and serum enzymes in carbon tetrachloride-treated rats

Toxicol Pathol. 1995 Jul-Aug;23(4):439-46. doi: 10.1177/019262339502300401.

Abstract

We evaluated various biomarkers associated with cell proliferation immediately following insult with the classic hepatotoxicant carbon tetrachloride (CCl4). Rats were administered a single necrogenic dose of CCl4 and euthanized at either t = 4, 8, 12, 16, or 24 hr postdose. Parameters evaluated included the following: immunohistochemical detection of hepatocellular proliferating cell nuclear antigen labeling indices (PCNA-LIs; percentage of cells in S phase) and growth fractions (PCNA-GFs; percentage of cells in the cell cycle); PCNA and the cyclin-dependent kinase p34cdc2 (CDK) protein in S-9 fractions by Western blot and enzyme-linked immunosorbent assay (ELISA); and liver-related serum enzymes. An increase in PCNA-GF was observed at t = 4 hr, concomitant with elevations in CDK and PCNA protein (Western blot). PCNA-LIs were increased by t = 24 hr, as were CDK and PCNA by ELISA. Sorbitol dehydrogenase was the most sensitive enzyme, with increases observed at t = 4 hr. Our results indicate that PCNA-GF, CDK, and PCNA levels reflect hepatocellular regeneration as early as 4 hr following CCl4 insult. We conclude that these assays are early and sensitive indicators of acute hepatotoxicity that may be advantageous to evaluate in the early stages of exploratory studies.

Publication types

  • Comparative Study

MeSH terms

  • Alanine Transaminase / blood*
  • Animals
  • Aspartate Aminotransferases / blood*
  • CDC2 Protein Kinase / drug effects*
  • Carbon Tetrachloride*
  • Cyclin-Dependent Kinases / drug effects
  • Immunohistochemistry
  • Liver / chemistry*
  • Liver / enzymology
  • Liver / immunology
  • Male
  • Mitotic Index / drug effects*
  • Proliferating Cell Nuclear Antigen / drug effects*
  • Rats
  • Rats, Sprague-Dawley
  • S Phase / drug effects*

Substances

  • Proliferating Cell Nuclear Antigen
  • Carbon Tetrachloride
  • Aspartate Aminotransferases
  • Alanine Transaminase
  • CDC2 Protein Kinase
  • Cyclin-Dependent Kinases