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Molecular Pharmacology, Vol 4, 427-434, Copyright © 1968 by the American Society for Pharmacology and Experimental Therapeutics
1 The Ben May Laboratory for Cancer Research, The University of
Chicago, Illinois 60637
Pulse-doses of 7,12-dimethylbenz[a]anthracene and 7,8,12-trimethylbenz[a]anthracene share a remarkable ability to damage selectively endocrine glands and targets of hormones in female rodents. Both compounds depress synthesis of DNA in ileum and spleen.
In CF-1 mice, 7,12-dimethylbenz[a]anthracene and 7,8,12-trimethylbenz[a]anthracene severely injured the ovary and elicited ovarian tumors and leukemia, whereas the adrenal was uninjured by these compounds. 3-Methylcholanthrene and benzo[a]pyrene induced leukemia, but ovarian tumors did not develop.
In adult rats, a pulse-dose of 7,8,12-trimethylbenz[a]anthracene caused adrenal apoplexy but did not evoke ovarian tumors.
Note:
ACKNOWLEDGMENTS
Lipid emulsions of hydrocarbons were prepared
by P. E. Schurr, The Upjohn Company, Kalamazoo, Michigan. We are grateful to Eugene
DeSombre, Ben May Laboratory for Cancer Research, The University of Chicago, for measurement of radioactivity.