Potter C L, Sipes I G, Russell D H
Biochem Pharmacol. 1982 Nov 1;31(21):3367-71. doi: 10.1016/0006-2952(82)90613-x.
The effects of 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) on the activity of rat liver ornithine decarboxylase (ODC) were investigated. Sixteen hours after partial hepatectomy, rats that had been pretreated with TCDD for 1 week exhibited a 3- to 4-fold increase in ODC activity, while vehicle controls exhibited to 8- to 10-fold increase. This inhibition of ODC induction by TCDD was time dependent since TCDD administration at the time of partial hepatectomy did not produce inhibitory effects on the subsequent ODC induction. ODC induction after either aminophylline or dexamethasone administration, agents which act via cAMP-mediated and direct nuclear events, respectively, also was inhibited by pretreatment with TCDD. It was concluded that TCDD pretreatment decreased the ability of the liver to respond to hormonal stimulation as reflected in the attenuation of ODC induction. RNA polymerase I activity, which positively correlates with ODC activity in growth and development, decreased concomitantly with decreased induction of ODC. In unstimulated liver RNA polymerase I activity, as well as protein, DNA, and RNA levels, remained unchanged 1 week after TCDD. However, TCDD administration resulted in decreased liver concentrations of putrescine and spermidine, but not spermine. This suggests that TCDD pretreatment results in a time-dependent decrease in hormone responsivity.
研究了2,3,7,8-四氯二苯并对二恶英(TCDD)对大鼠肝脏鸟氨酸脱羧酶(ODC)活性的影响。部分肝切除术后16小时,用TCDD预处理1周的大鼠ODC活性增加了3至4倍,而溶剂对照组的ODC活性增加了8至10倍。TCDD对ODC诱导的这种抑制作用是时间依赖性的,因为在部分肝切除时给予TCDD对随后的ODC诱导没有产生抑制作用。氨茶碱或地塞米松给药后(分别通过cAMP介导和直接核事件起作用的药物)的ODC诱导也受到TCDD预处理的抑制。得出的结论是,TCDD预处理降低了肝脏对激素刺激的反应能力,这在ODC诱导的减弱中得到体现。在生长和发育过程中与ODC活性呈正相关的RNA聚合酶I活性,随着ODC诱导的减少而相应降低。在未受刺激的肝脏中,TCDD处理1周后RNA聚合酶I活性以及蛋白质、DNA和RNA水平保持不变。然而,给予TCDD导致肝脏中腐胺和亚精胺的浓度降低,但精胺浓度未降低。这表明TCDD预处理导致激素反应性随时间下降。