Seifert J, Pewnim T
Department of Environmental Biochemistry, University of Hawaii, Honolulu 96822.
Biochem Pharmacol. 1992 Dec 1;44(11):2243-50. doi: 10.1016/0006-2952(92)90353-k.
Diazinon [O,O-diethyl O-(2-isopropyl-6-methyl-4- pyrimidinyl)phosphorothioate] altered the formation of several L-tryptophan metabolites associated with the L-kynurenine pathway in mice. Liver kynurenine formamidase was inhibited almost completely by diazinon (10 mg/kg). The enzyme inhibition resulted in reduced L-kynurenine biosynthesis in livers with a concomitant accumulation of N-formyl-L-kynurenine. In contrast to the liver, plasma L-kynurenine increased up to 5-fold in diazinon-treated mice. Consequently, the urinary excretion of xanthurenic acid and kynurenic acid was raised 5- to 15-fold. The revelation of this novel mechanism of diazinon action is an important piece of information needed for a better understanding of the noncholinergic toxicity of organophosphorous acid triesters and methylcarbamates.
二嗪农[O,O-二乙基-O-(2-异丙基-6-甲基-4-嘧啶基)硫代磷酸酯]改变了小鼠体内与L-犬尿氨酸途径相关的几种L-色氨酸代谢产物的形成。二嗪农(10毫克/千克)几乎完全抑制了肝脏犬尿氨酸甲酰胺酶。这种酶抑制导致肝脏中L-犬尿氨酸生物合成减少,同时N-甲酰-L-犬尿氨酸积累。与肝脏相反,在经二嗪农处理的小鼠中,血浆L-犬尿氨酸增加了5倍。因此,尿中黄尿酸和犬尿酸的排泄量增加了5至15倍。揭示二嗪农作用的这一新机制是更好地理解有机磷酸三酯和甲基氨基甲酸酯非胆碱能毒性所需的重要信息。