Identification of sensitive and novel
biomarkers or endpoints associated with toxicity and
carcinogenesis is of a high priority. There is increasing interest in the incorporation of epigenetic and metabolic
biomarkers to
complement apical data; however, a number of questions, including the tissue specificity, dose-response patterns, early detection of those endpoints, and the added value need to be addressed. In this study, we investigated the dose-response relationship between apical, epigenetic, and metabolomics endpoints following short-term exposure to experimental hepatotoxicants,
clofibrate (CF) and
phenobarbital (PB). Male F344 rats were exposed to PB (0, 5, 25, and 100 mg/kg/day) or CF (0, 10, 50, and 250 mg/kg/day) for seven days. Exposure to PB or CF resulted in dose-dependent increases in relative liver weights, hepatocellular
hypertrophy and proliferation, and increases in
Cyp2b1 and Cyp4a1 transcripts. These changes were associated with altered histone modifications within the regulatory units of
cytochrome genes, LINE-1
DNA hypomethylation, and altered
microRNA profiles. Metabolomics data indicated alterations in the metabolism of
bile acids. This study provides the first comprehensive analysis of the apical, epigenetic and metabolic alterations, and suggests that the latter two occur within or near the dose response curve of apical endpoint alterations following exposure to experimental hepatotoxicants.