Record Display for the EPA National Library Catalog
RECORD NUMBER: 603 OF 2888
|OLS Field Name||OLS Field Data|
|Main Title||Comparative Study of Two Polychlorinated Biphenyl Mixtures (Aroclors 1242 and 1016) Containing 42% Chlorine on Induction of Hepatic Porphyria and Drug Metabolizing Enzymes.|
|Author||Goldstein, Joyce A. ; Hickman, Patricia ; Burse, Virlyn W. ; Bergman., Hinda ;|
|CORP Author||National Environmental Research Center, Research Triangle Park, N.C.|
|Report Number||found in PB-280 889|
|Stock Number||PB-280 893, found in PB-280 889|
|Additional Subjects||Pesticides ; Toxicology ; Bioassay ; Laboratory animals ; Chlorine organic compounds ; Rats ; Ingestion(Biology) ; Metabolism ; Liver ; Porphyria ; Metabolic diseases ; Enzymes ; Drug ; Physiological effects ; Experimental data ; Comparison ; Concentration(Composition) ; Tables(Data) ; Polychlorinated biphenyls ; Reprints ; Aroclor 1016 ; Toxic substances ; Aroclor 1242 ; Biological effects ; Bioaccumulation ; Pesticide residues ; Biphenyl/chloro|
Aroclor 1242 and Aroclor 1016 are polychlorinated biphenyl (PCB) mixtures with similar chlorine content (42 vs 41%), but Aroclor 1242 contains 9% biphenyl homologs with five or more chlorines while Aroclor 1016 contains only 1%. The effects of Aroclor 1242 and Aroclor 1016 on induction of hepatic porphyria and drug-metabolizing enzymes were compared in female rats fed 100 ppm or 500 ppm of each. At 1 wk, Aroclor 1242 markedly increased liver weight and all drug-metabolizing pathways tested including cytochrome P-450, liver weight, N-demethylase, nitroreductase, aniline hydroxylase, and glucuronyl transferase, while Aroclor 1016 had produced only very minimal effects. At 6 mo, however, 500 ppm of either Aroclor markedly increased drug-metabolism, while at the lower dose, Aroclor 1016 was much less effective than Aroclor 1242. Both doses of Aroclor 1242 produced prophyria, but only the higher dose of Aroclor 1016 was prophyrogenic. The porphyria occurred after a lag of 1-6 mo and was characterized by excretion and hepatic storage or uroporphyrins. Aroclor tissue concentrations were similar in rats fed equal doses of the two mixtures. Therefore, the marked differences in the biological effects of Aroclor 1016 and Aroclor 1242 cannot be explained by differences in absorption, metabolism, or excretion.
contained in PB 280 889 titled Journal articles on Toxicology. Group 14.