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有机磷酸酯对大鼠肝微粒体中UDP-葡萄糖醛酸基转移酶活性的选择性抑制作用。

Selective inhibitory effect of organophosphates on UDP-glucuronyl transferase activities in rat liver microsomes.

作者信息

Watanabe H K, Hoskins B, Ho I K

出版信息

Biochem Pharmacol. 1986 Feb 1;35(3):455-60. doi: 10.1016/0006-2952(86)90219-4.

Abstract

The effects of acute and subacute administration of diisopropylfluorophosphate (DFP) and acute administration of Soman, Sarin and Tabun on UDP-glucuronyltransferase (GT) activity towards 4-nitrophenol, 4-methylumbelliferone, phenolphthalein and testosterone in rat liver microsomes were investigated. Twenty-four hours after a single injection of DFP, the activity of GT towards 4-nitrophenol and 4-methylumbelliferone was inhibited, and the inhibitory effect continued for 3 days. The activity had recovered by 7 days after injection. The activity of GT towards phenolphthalein and testosterone was not affected at any time after injection. Soman, Sarin and Tabun showed the same effect as DFP after a single injection. After daily DFP injections, the activity of GT towards 4-nitrophenol and 4-methylumbelliferone was decreased to the same level as found following acute treatment with DFP. The in vitro addition of DFP to liver microsomes did not affect GT activity towards 4-nitrophenol. It is suggested that these changes are not due to a direct effect of DFP. Furthermore, the effects of two enzyme inducers on GT activity in the presence and absence of DFP were investigated. In the 3-methylcholanthrene (MC) pretreatment group, DFP inhibited only the GT activity towards 4-nitrophenol and 4-methylumbelliferone. On the other hand, in the phenobarbital (PB) pretreatment group, DFP did not inhibit the GT activity towards 4-nitrophenol and 4-methylumbelliferone. It was also demonstrated that MC pretreatment increased the mortality in the DFP-treated rats but that PB pretreatment suppressed it. These results suggest that DFP and other organophosphorus agents may be useful agents for studies on the heterogeneity of GT.

摘要

研究了二异丙基氟磷酸酯(DFP)急性和亚急性给药以及梭曼、沙林和塔崩急性给药对大鼠肝微粒体中UDP-葡萄糖醛酸基转移酶(GT)催化4-硝基苯酚、4-甲基伞形酮、酚酞和睾酮反应活性的影响。单次注射DFP 24小时后,GT对4-硝基苯酚和4-甲基伞形酮的活性受到抑制,且这种抑制作用持续3天。注射后7天活性恢复。注射后任何时间GT对酚酞和睾酮的活性均未受影响。单次注射后,梭曼、沙林和塔崩表现出与DFP相同的作用。每日注射DFP后,GT对4-硝基苯酚和4-甲基伞形酮的活性降低至与DFP急性处理后相同的水平。体外向肝微粒体中添加DFP不影响GT对4-硝基苯酚的活性。提示这些变化并非由DFP的直接作用引起。此外,研究了两种酶诱导剂在有和无DFP存在时对GT活性的影响。在3-甲基胆蒽(MC)预处理组中,DFP仅抑制GT对4-硝基苯酚和4-甲基伞形酮的活性。另一方面,在苯巴比妥(PB)预处理组中,DFP不抑制GT对4-硝基苯酚和4-甲基伞形酮的活性。还证明MC预处理增加了DFP处理大鼠的死亡率,但PB预处理可抑制这种死亡率。这些结果表明,DFP和其他有机磷试剂可能是研究GT异质性的有用试剂。

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