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Methapyrilene Toxicity: Anchorage of Pathologic Observations to Gene Expression AlterationsNational Institute of Environmental Health Sciences, Research Triangle Park, North Carolina 27709, USA
Boehringer Ingelheim Pharmaceuticals Inc, Ridgefield, Connecticut 06877, USA
National Institute of Environmental Health Sciences, Research Triangle Park, North Carolina 27709, USA
National Institute of Environmental Health Sciences, Research Triangle Park, North Carolina 27709, USA
National Institute of Environmental Health Sciences, Research Triangle Park, North Carolina 27709, USA
National Institute of Environmental Health Sciences, Research Triangle Park, North Carolina 27709, USA
Boehringer Ingelheim Pharmaceuticals Inc, Ridgefield, Connecticut 06877, USA
Boehringer Ingelheim Pharmaceuticals Inc, Ridgefield, Connecticut 06877, USA
Boehringer Ingelheim Pharmaceuticals Inc, Ridgefield, Connecticut 06877, USA
National Institute of Environmental Health Sciences, Research Triangle Park, North Carolina 27709, USA
National Institute of Environmental Health Sciences, Research Triangle Park, North Carolina 27709, USA
National Institute of Environmental Health Sciences, Research Triangle Park, North Carolina 27709, USA
National Institute of Environmental Health Sciences, Research Triangle Park, North Carolina 27709, USA, paules{at}niehs.nih.gov. Methapyrilene (MP) exposure of animals can result in an array of adverse pathological responses including hepatotoxicity. This study investigates gene expression and histopathological alterations in response to MP treatment in order to 1) utilize computational approaches to classify samples derived from livers of MP treated rats based on severity of toxicity incurred in the corresponding tissue, 2) to phenotypically anchor gene expression patterns, and 3) to gain insight into mechanism(s) of methapyrilene hepatotoxicity. Large-scale differential gene expression levels associated with the exposure of male Sprague—Dawley rats to the rodent hepatic carcinogen MP for 1, 3, or 7 days after daily dosage with 10 or 100 mg/kg/day were monitored. Hierarchical clustering and principal component analysis were successful in classifying samples in agreement with microscopic observations and revealed low-dose effects that were not observed histopathologically. Data from cDNA microarray analysis corroborated observed histopathological alterations such as hepatocellular necrosis, bile duct hyperplasia, microvesicular vacuolization, and portal inflammation observed in the livers of MP exposed rats and provided insight into the role of specific genes in the studied toxicological processes.
Key Words: Toxicogenomics • gene expression • methapyrilene • toxicity classification • rat liver • histopathology • phenotypic anchorage • hepatotoxicity.
Toxicologic Pathology, Vol. 30, No. 4,
470-482 (2002) This article has been cited by other articles:
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