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)pyrene1
The The Wellcome Research Laboratories, Burroughs Wellcome & Co. (U. S. A.) Inc., Tuckahoe, New York 10707
Pretreatment of rats with benzo(
)pyrene, 3-methylcholanthrene, or 7,12-dimethylbenz(
)anthracene p.o. once daily for two days prior to the i.v. administration of tritiated benzo(
)-pyrene (BP-3H) on the third day stimulates the disappearance of BP-3H from blood and decreases the concentration of BP-3H in various tissues. Pretreatment of rats with pyrene, anthracene, or phenobarbital does not stimulate the in vivo disappearance of BP-3H. The concentration of BP-3H in the fat of rats is lower after seven daily p.o. doses of BP-3H than after a single dose of BP-3H, which suggests that this hydrocarbon stimulates its own metabolism during chronic administration.
1 This study was supported in part by Research Contract PH 43-65-1066 from the Pharmacology-Toxicology Programs, National Institute of General Medical Sciences, NIH.
2 Present address: Pharmakologisches Institut der Freien Universität, (Abt. Embryonal-Pharmakologie), 1 Berlin-Dahlem (33), Thielallee 69/73, West Germany.
3 Present address: Department of Biochemistry, Hoffmann-La Roche, Inc., Nutley, N. J. 07110.
4 Present address: Technicon Corporation, 511 Benedict Avenue, Tarrytown, N. Y. 10591.
Received 5/ 1/70. Accepted 8/19/70.
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