Abstract |
The ultimate carcinogenic form of benzo(a)pyrene (BP) is thought to result from metabolic activation at the 7 to 10 positions. Substitution by a methyl group at these positions would be expected to inhibit strongly their metabolism even though 7-methylbenzo(a)pyrene (7-MeBP) has been reported to be carcinogenic in some tumor models. The metabolism of 7-MeBP was, therefore, studied using both microsomal preparations and whole cells, the products being analyzed by high-pressure liquid chromatography, fluorescence spectrophotometry, and mass spectrometry. These studies revealed that many of the expected metabolites were formed by microsomes, but in addition 7-MeBP yielded a compound which was isolated and identified as trans-7,8-dihydro-7,8-dihydroxy-7-methylbenzo(a)pyrene. These results indicate that, despite the presence of a methyl group at the 7 position, a substituted BP can undergo the same initial metabolic activation as BP itself. However, in contrast to BP, the 7,8-dihydrodiol formed from 7-MeBP was almost racemic, and neither enantiomer was very active in the Ames bacterial mutagenesis assay when compared with trans-7,8-dihydro-7,8-dihydroxybenzo(a)pyrene. The metabolism of 7-MeBP was also studied in 10T1/2 cells. The hydrocarbon was metabolized readily and bound to DNA of the cells to about one-eighth of the level found for BP. However, no 7,8-dihydro-7,8-dihydroxy-7-methylbenzo(a)pyrene could be detected in the culture medium.
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Authors | T Kinoshita, M Konieczny, R Santella, A M Jeffrey |
Journal | Cancer research
(Cancer Res)
Vol. 42
Issue 10
Pg. 4032-8
(Oct 1982)
ISSN: 0008-5472 [Print] United States |
PMID | 7049354
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, P.H.S.)
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Chemical References |
- Benzopyrenes
- 7-methylbenzo(a)pyrene
- DNA
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Topics |
- Animals
- Benzopyrenes
(metabolism, pharmacology)
- Biotransformation
- Cells, Cultured
- Chromatography, High Pressure Liquid
- Circular Dichroism
- DNA
(metabolism)
- Mice
- Microsomes, Liver
(metabolism)
- Mutagenicity Tests
- Mutation
- Rats
- Salmonella typhimurium
(drug effects)
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