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Metabolism of benzo(a)pyrene and 7,12-dimethylbenz(a)anthracene in cultured human fetal aortic smooth muscle cells

Journal Article · · Life Sci.; (United States)
Cultured human fetal aortic smooth muscle cells derived from the abdominal aorta converted benzo(a)pyrene (BaP) and 7,12-dimethylbenz(a)anthracene (DMBA) via cytochrome P-450-dependent monooxygenation to metabolites detectable by both a highly sensitive radiometric assay and high pressure liquid chromatography (HPLC). Cells incubated with /sup 3/H-BaP transformed this substrate primarily to phenols. /sup 14/C-DMBA was converted to metabolites that cochromatographed with 12-hydroxymethyl-methylbenz(a)anthracene, 7-hydroxymethyl-12-methylbenz(a)anthracene, 7- 7,12-dihydroxymethylbenz(a)anthracene, and trans-8,9-dihydrodiol-7,12-DMBA. Exposure of cells in culture to 13 ..mu..M 1,2-benz(a)anthracene resulted in increased oxidative metabolism of both BaP and DMBA. In the case of BaP, total phenol formation was increased, while with DMBA all metabolites detected by HPLC were increased. Support for the potential role of metabolism of polycyclic aromatic hydrocarbons by aortic smooth muscle cells in the etiology of atherosclerosis was obtained.
Research Organization:
Univ. of Washington, Seattle
OSTI ID:
6783511
Journal Information:
Life Sci.; (United States), Journal Name: Life Sci.; (United States) Vol. 25:5; ISSN LIFSA
Country of Publication:
United States
Language:
English

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