TY - JOUR T1 - ENZYMATIC BASIS OF CYCLOPHOSPHAMIDE ACTIVATION BY HEPATIC MICROSOMES OF THE RAT JF - Journal of Pharmacology and Experimental Therapeutics JO - J Pharmacol Exp Ther SP - 206 LP - 210 VL - 174 IS - 2 AU - J. L. COHEN AU - J. Y. JAO Y1 - 1970/08/01 UR - http://jpet.aspetjournals.org/content/174/2/206.abstract N2 - Our data confirm and enhance the thesis that the activation of cyclophosphamide by liver is mediated through the mixed function oxidase system involved in the metabolism of drugs, steroids and carcinogens. This is based on the following lines of evidence. First, the enzyme is located primarily if not exclusively in liver microsomes. Second, the enzyme requires reduced triphosphopyridine nucleotide and molecular oxygen for full activity. Third, the enzyme is inhibited in vitro by compounds known to be metabolized by the mixed function oxidase system of liver microsomes such as hexobarbital and steroids and the kinetics of inhibition by hexobarbital is that of a competitive type. Fourth, the enzyme can be inhibited by carbon monoxide as well as other compounds known to interrupt the microsomal electron transport chain such as p-hydroxymercuribenzoate and cytochrome c. Fifth, the enzyme level is markedly increased by phenobarbital administration. Finally, there is a clear sex-related difference in concentration of this enzyme in the rat liver. Evidence is presented that the induction of cyclophosphamide-activating enzyme by phenobarbital can be correlated with an enhancement of the pharmacologic effect of cyclophosphamide in the laboratory animal. © 1970 by The Williams & Wilkins Co. ER -