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Application of a statistical dynamic model investigating the short-term cellular kinetics induced by riddelliine, a hepatic endothelial carcinogen.

Abstract
In recent studies, riddelliine, a pyrrolizidine alkaloid, was found to increase rates of replication and apoptosis and induce hemangiosarcoma in the liver of rats and mice. To analyze DNA replication and apoptosis data taken from the same animals, we have developed a predictive mathematical model for describing BrdU labeling and apoptotic processes. The model allows the incorporation of simple diurnal patterns in cellular kinetics and is applied to data on hepatocytes and endothelial cells taken from riddelliine exposed rats. Predictions from the model were used with multivariable nonlinear regression techniques to estimate replication and apoptotic rate constants for both cell types and all treatment groups. Hypothesis tests were used with the predicted rates to separate the competing effects of riddelliine on replication and apoptosis of hepatocytes and endothelial cells as well as compare replication rates between cell types. That estimated replication rates were found to be significantly higher for endothelial cells supports the supposition of induction of hemangiosarcoma by riddelliine in the liver.
AuthorsMarjo V Smith, Abraham Nyska, Chris Portier
JournalToxicological sciences : an official journal of the Society of Toxicology (Toxicol Sci) Vol. 80 Issue 2 Pg. 258-67 (Aug 2004) ISSN: 1096-6080 [Print] United States
PMID15129021 (Publication Type: Journal Article)
Chemical References
  • Carcinogens
  • Pyrrolizidine Alkaloids
  • riddelliine
Topics
  • Algorithms
  • Animals
  • Apoptosis (drug effects)
  • Carcinogens (pharmacokinetics, toxicity)
  • Cell Count
  • Cell Proliferation (drug effects)
  • Cells (metabolism)
  • DNA Replication (drug effects)
  • Endothelium (pathology)
  • Hemangiosarcoma (chemically induced, pathology)
  • Hepatocytes (drug effects, pathology)
  • Least-Squares Analysis
  • Liver Neoplasms (chemically induced, pathology)
  • Male
  • Models, Statistical
  • Pyrrolizidine Alkaloids (pharmacokinetics, toxicity)
  • Rats
  • Rats, Inbred F344

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