THE PROTECTIVE ACTION OF GLUTATHIONE ON THE MICROBIAL MUTAGENICITY OF THE Z-ISOMER AND E-ISOMER OF 1,3-DICHLOROPROPENE

The Z(cis)- and E(trans)-isomers of 1,3-dichloropropene (DCP) [soil fumigant], in confirmation of previous reports, caused dose-dependent increases in the numbers of reverse mutations in Salmonella typhimurium TA100 in the presence and absence of a 9000 .times. g supernatant fraction (S9) from the livers of Aroclor-treated rats. The relevance of these findings to mammals is uncertain, not least because of major differences in the metabolism of the DCP in the microbial assay systems and in vivo. For example, (Z)-DCP is efficiently detoxified in mammals by the operation of a glutathione (GSH)-dependent S-alkyl transferase. It is possible that such detoxification could proceed only very slowly in the microbial assays because the concentrations of GSH could be severely rate-limiting even in those assays fortified by the addition of S9. A dramatic reduction in the microbial mutagenicity of both (Z)-and (E)-DCP was observed when the concentration of GSH in the microbial assays was adjusted to a normal physiological concentration (5 mM). This protective action of GSH was at least as effective in the absence of S9 as in its presence, suggesting that it was not mediated by mammalian GSH transferase. There appears to be little or no GSH alkyl or aryl transferase in the cytosol of S. typhimurium TA100, but intracellular GSH is present at a concentration similar to that found in mammalian cells. Since the uncatalyzed reaction between the DCP and glutathione is relatively slow, the effect is not due simply to their destruction by GSH. A physiological concentration of extracellular GSH could maintain the intracellular GSH in a reduced form in which its nucleophilic thiol group competes effectively with the nucleophilic centers in the bacterial DNA for the haloalkenes. The efficiency of GSH-linked systems in affording protection against the genotoxic action of the DCP is considered. It may be presumed that their operation would exert a major limiting effect on the genotoxicity of (Z)- and (E)-DCP in mammals.