Cutaneous metabolism of benzo[a]pyrene: comparative studies in C57BL/6N and DBA/2N mice and neonatal Sprague--Dawley rats |
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Authors: | D R Bickers H Mukhtar S K Yang |
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Institution: | 2. Department of Dermatology, Case Western Reserve University School of Medicine and the Veterans Administration Medical Center, Cleveland, OH 44106 U.S.A.;1. Department of Pharmacology, School of Medicine, Uniformed Services University of the Health Sciences, Bethesda, MD 20814 U.S.A. |
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Abstract: | The metabolism of the polycyclic aromatic hydrocarbon (PAH) carcinogen benzoa]pyrene (BaP) was studied using microsomes prepared from the skin of the mouse and rat. Topical application of the polychlorinated biphenyl (PCB) Aroclor 1254 or the PAH 3-methylcholanthrene (3-MC) to the skin of the C57BL/6N and DBA/2N mouse and the Sprague-Dawley rat caused statistically significant enhancement of cutaneous microsomal aryl hydrocarbon hydroxylase (AHH) activity in each animal. PCB was a more potent inducer of the enzyme than was 3-MC. BaP metabolism by skin microsomes from the same animals was assessed using high performance liquid chromatography (HPLC). The skin of untreated animals metabolized BaP into 9,10-, 7,8- and 4,5-dihydrodiols, phenols and quinones. Skin application of PCB caused greater than 16–18-fold enhancement of BaP metabolism in the C57BL/6N mouse and the rat and 2–5-fold enhancement in the DBA/2N mouse. Skin application of 3-MC enhanced BaP metabolism 2–8-fold in the C57BL/6N mouse and 5–10-fold in the rat and had no effect in the DBA/2N mouse. The formation of procarcinogenic metabolite BaP-7, 8-diol was greatly enhanced (4–12-fold) by treatment with the PCB and 3-MC in the tumor susceptible C57BL/6N mouse and in the tumor-resistant neonatal Sprague-Dawley rat. In contrast, the formation of BaP-7,8-diol was either slightly enhanced (2-fold) or unaffected by treatment with the PCB or 3-MC in the tumor-resistant DBA/2N mouse. Our data indicate that neither the patterns of metabolism nor the amount of BaP-7,8-diol formation in the skin are reliable predictors of tumor susceptibility to the PAH in rodent skin. |
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Keywords: | AHH aryl hydrocarbon hydroxylase BaP HPLC high pressure liquid chromatography 3-MC 3-methylcholanthrene PAH polycyclic aromatic hydrocarbon PCB polychlorinated biphenyl Skin Carcinogen Metabolism High performance liquid chromatography |
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