Selenium suppresses the metabolism of benzo[a]pyrene by rat-liver extracts, and exerts a dual effect on its mutagenicity

Abstract
1. Liver homogenates from rats injected with 3 -methylcholanthrene were employed for metabolism of benzo[a]pyrene (BP) and in assays of aryl hydrocarbon hydroxylase (AHH) activity in vitro. 2. Sodium selenite inhibited AHH activity to a maximum of ∼70%. It suppressed the overall metabolism of benzo[a]pyrene; a distinct reduction in the products was evident on h.p.l.c. analysis. 3. Sodium thiosulphate also inhibited AHH activity by ∼ 47%. Inclusion of S2O2-3 and SeO2-3, in combination, led to a cumulative inhibition of 87%. 4. The mutagenicity of BP in the Salmonella auxotroph reversion system (Ames test) was enhanced by SeO2-3 at concentrations below 0.2 mM. Above this level a significant anti-mutagenic effect was observed.

This publication has 24 references indexed in Scilit: