## LSU Historical Dissertations and Theses

1998

Dissertation

#### Degree Name

Doctor of Philosophy (PhD)

#### Department

Veterinary Physiology, Pharmacology, and Toxicology (Veterinary Medical Sciences)

Jay C. Means

#### Abstract

There is special concern about the potential health effects of by-products released into the environment after combustion or conversion of fossil fuels. Polycyclic aromatic hydrocarbons (PAH), while initially released largely into the atmosphere, are subsequently deposited in soil and water and on foods. Although the significance of PAH contamination with regard to environmentally caused diseases and cancer in humans is difficult to estimate, it is suggested that the potential hazards may be underestimated. In an effort to understand the potential adverse health effects of PAHs, a comprehensive study was undertaken to determine the metabolic fate of selected PAHs as individual agents and as components of a mixture following oral exposure in the Fischer-344 rat. Studies included radioisotope binding studies to evaluate the absorption, distribution, and elimination of selected compounds, acute toxicity trials to define maximum tolerated chemical concentration levels, and chronic studies to determine temporal effects of individual compounds and the mixture. Selected compounds included 2-aminoanthracene (2-AA), benz (a) anthracene (BA), and the 1,3-; 1,6-, and 1,-8-dinitropyrenes (DNP). Results of radioisotope binding studies and ingestion studies clearly indicated that toxicity of BA or DNP were minimal in exposed rats. Administration of 50$\mu$Ci per kg ($\sp3$H) -BA (10mg/kg) or ($\sp3$H) -DNP (10mg/kg) via oral gavage resulted in a rapid excretion of greater than 70% of the recovered label at 48 h. Similarly, when rats were fed BA or dinitropyrenes (DNP) at concentrations up to 0.1% of the diet toxic effects were not observed following 14-, 30-, or 80-days of exposure. In contrast administration of 2-AA at concentration levels as low as 0.0075% of the diet resulted in a temporal and dose response progression in toxic effects of the liver and pancreas. Hepatocellular hyperplastic nodules were detected in rat liver following 80 days of ingestion of 2-AA at 0.01% and 0.0075% of diet. 2-AA pancreatic toxicity resulted in large cytoplasmic vacuoles and almost complete depletion of insulin stores in the endocrine pancreas and necrotic changes in the exocrine pancreas. Attenuation of the toxic effects of 2-AA was demonstrated in rats fed a mixture of the same compounds at the same dietary level of incorporation.

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