THE INTERFERENCE OF POLYCHLORINATED-BIPHENYLS (AROCLOR-1254) WITH MEMBRANE REGULATION OF THE ACTIVITIES OF CYTOCHROME-P-450C21 AND CYTOCHROME-P-45017-ALPHA,LYASE IN GUINEA-PIG ADRENAL MICROSOMES

Regulation of cytochromes P-450 21-hydroxylase (P-450C21) and P-450 17-alpha-hydroxylase/C17,20-lyase (P-450(17-alpha,lyase)) activities and impairment of this regulation by Aroclor 1254 was studied in guinea-pig adrenal microsomes. In a membrane depleted system, a decrease in the normally predominant, P-450C21 activity and an increase in P-450(17-alpha,lyase) activities was observed. The same deviations were observed in intact microsomes with increase in the reaction temperature (0-40-degrees-C). Breaks in Arrhenius plots for activities of P-450C21 and P-450(17-alpha,lyase) correlate with transition temperatures reported for the microsomal membrane. These results point to: (1) preference of a gel state membrane for catalytic expression of P-450C21 suggesting a clustered organization of this P-450 species with reductase; (2) preference of a fluid membrane for lyase activity suggesting a random collision mechanism for reduction of P-450(17-alpha,lyase). Aroclor 1254 introduced to reaction mixtures containing intact microsomes elicited basically the same changes as caused by depletion of the microsomal membrane or by increase in the incubation temperature. Lack of effect of Aroclor 1254 on P-450C21 and P-450(17-alpha,lyase) activities in the membrane depleted system demonstrates that its interference with monooxygenase activities is mediated by the microsomal membrane. The similarities between altered cytochrome P-450 mediated activities in the presence of Aroclor 1254 and the deviations observed in the membrane depleted system or upon increase in the incubation temperature may suggest that this chemical exerts its impacts by influencing membrane fluidity.