Arrhenius E, Renberg L, Johansson L, Zetterqvist M A
Chem Biol Interact. 1977 Jul;18(1):35-46. doi: 10.1016/0009-2797(77)90139-9.
The pesticide pentachlorophenol known as an uncoupler of mitochondrial oxidative phosphorylation was shown to disturb liver microsomal detoxication functions by a selective inhibition of the terminal oxygenation enzyme P-450. At lower concentrations the flavin moiety of this enzyme chain is not inhibited but rather is stimulated, whereby a qualitative shift in detoxication of aromatic amines from C-oxygenation to N-oxygenation is obtained. The effects were due to the pentachlorophenol itself and not to a metabolite. Similar effects of varying strength were also obtained with other chlorophenol pesticides; 2,4,di-, 2,4,6,-tri and 2,3,4,6-tetrachlorophenol, di- and hexachlorophen, tri- and nonachloro-2-hydroxydiphenyl ethers. The relevance of these findings to the possible synergistic influence of chlorophenols on the carcinogenic effects of polyaromatic amines and hydrocarbons is discussed.
农药五氯苯酚被认为是线粒体氧化磷酸化的解偶联剂,它通过选择性抑制末端加氧酶P - 450来干扰肝脏微粒体的解毒功能。在较低浓度下,该酶链的黄素部分未受抑制,反而受到刺激,从而使芳香胺的解毒从碳加氧转变为氮加氧,实现了定性转变。这些影响是由五氯苯酚本身造成的,而非其代谢产物。其他氯酚类农药,如2,4 - 二氯苯酚、2,4,6 - 三氯苯酚、2,3,4,6 - 四氯苯酚、二氯苯酚和六氯苯酚、三氯和九氯 - 2 - 羟基二苯醚,也产生了强度各异的类似效果。本文讨论了这些发现与氯酚类物质对多环芳烃和多环胺致癌作用可能产生的协同影响之间的相关性。