Oguro T, Numazawa S, Yoshida T, Kuroiwa Y
Department of Biochemical Toxicology, School of Pharmaceutical Sciences, Showa University, Tokyo, Japan.
Biochem Biophys Res Commun. 1987 Oct 14;148(1):422-8. doi: 10.1016/0006-291x(87)91128-4.
The administration of Phorone (diisopropylidene acetone, 250 mg/kg, ip.), a glutathione (GSH) depletor, markedly induced (400-fold of the control at 12 hr) ornithine decarboxylase (ODC) in the liver of rats. Parallel to ODC induction there was a marked increase in hepatic putrescine content. Phorone also produced an increase in spermidine content and a decrease in spermine content. The effects of phorone on ODC and putrescine content occurred dose-dependently with more than a 1000-fold increase in ODC activity over the controls at a dose of 500 mg/kg. Pretreatment of rats with buthionine sulfoximine, a GSH depletor by inhibition of biosynthesis, failed to inhibit phorone-mediated induction of ODC. In contrast, pretreatment with GSH, but not post-treatment, blocked the induction of ODC by phorone.
给予福罗酮(二亚异丙基丙酮,250毫克/千克,腹腔注射),一种谷胱甘肽(GSH)耗竭剂,可显著诱导(12小时时为对照组的400倍)大鼠肝脏中的鸟氨酸脱羧酶(ODC)。与ODC诱导同时发生的是肝脏腐胺含量显著增加。福罗酮还使亚精胺含量增加,精胺含量减少。福罗酮对ODC和腐胺含量的影响呈剂量依赖性,在500毫克/千克的剂量下,ODC活性比对照组增加了1000多倍。用丁硫氨酸亚砜胺预处理大鼠,一种通过抑制生物合成来耗竭GSH的物质,未能抑制福罗酮介导的ODC诱导。相反,用GSH预处理而非后处理可阻断福罗酮对ODC的诱导。