卡拉胶性炎症对苯巴比妥和苯并[a]芘诱导大鼠肝微粒体酶的影响。

M Ishikawa, K Sasaki, Y Takayanagi, K Sasaki
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引用次数: 3

摘要

用卡拉胶代谢系统诱导剂治疗大鼠,观察其对卡拉胶诱导炎症的抑制作用。分别给予苯巴比妥钠(PB, 80 mg/kg, i.p.,死亡前24 h)或苯并[a]芘(BP, 40 mg/kg, i.p.,死亡前24 h)作为诱导剂。一些动物也在死亡前24小时给予卡拉胶。非诱导雄性大鼠在卡拉胶处理后肝脏9000 x g上清(S-9)细胞色素P-450和氨基吡啶(AM) n-去甲基化酶、苯丙胺(BenzP) n-去甲基化酶和哌啶(MP) n-去甲基化酶活性显著降低。卡拉胶还抑制了PB处理对肝脏S-9细胞色素P-450含量的诱导,抑制了PB处理对AM、苯并、MP、芳烃和7-乙氧基coumarine代谢的诱导。大鼠细胞色素P-450水平和相关的生物转化活性在BP和卡拉胶同时注射后没有降低。未诱导、pb处理和bp处理的雌性大鼠均未表现出卡拉胶诱导的血红蛋白含量降低或am - n-去甲基化酶、BenzP n-去甲基化酶和苯胺羟化酶活性的抑制。这些结果表明,卡拉胶诱导的炎症对大鼠药物代谢的抑制作用具有选择性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effect of carrageenan-induced inflammation on the induction of hepatic microsomal enzymes by phenobarbital and benzo[a]pyrene in male rats.

The inhibitory effect of carrageenan-induced inflammation was examined by utilizing rats treated with inducers of this drug metabolizing system. Animals were given sodium phenobarbital (PB, 80 mg/kg, i.p., 24 h prior to death), or benzo[a]pyrene (BP, 40 mg/kg, i.p., 24 h prior to death) as inducers. Some animals were also given carrageenan 24 h prior to death. Non-induced male rats exhibited significant decreases in hepatic 9000 x g supernatant (S-9) cytochrome P-450 and aminopyrine (AM) N-demethylase, benzphetamine (BenzP) N-demethylase and meperidine (MP) N-demethylase activity following carrageenan treatment. Carrageenan also depressed the induction of hepatic S-9 cytochrome P-450 content caused by PB treatment, and suppressed the induction of AM, BenzP, MP, arylhydrocarbon and 7-ethoxycoumarine metabolism by PB treatment. Cytochrome P-450 levels and related biotransformation activity which are elevated by BP treatment were not decreased by the injection of BP and carrageenan simultaneously to male rats. Non-induced, PB-treated and BP-treated female rats did not show inhibited carrageenan-induced reduction in hemoprotein content or inhibition of AM-N-demethylase, BenzP N-demethylase and aniline hydroxylase activities. These results demonstrate the selective nature of the inhibitory effects of carrageenan-induced inflammation upon drug metabolism in the rats.

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