卡拉胶诱导的炎症对大鼠肝脏药物生物转化的抑制作用:性激素改变的影响。

M Ishikawa, K Sasaki, M Ozaki, Y Takayanagi, K Sasaki
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引用次数: 1

摘要

在体内用角叉菜胶处理后,发现大鼠肝脏药物代谢的改变存在性别差异。在成年雄性大鼠中,肝脏9000 x g上清细胞色素P-450含量显著降低,六巴比妥、氨基比林、乙基吗啡和哌替啶的生物转化也明显降低。与相应的对照组相比,卡拉胶治疗在完整和睾丸切除的动物中显著延长了六巴比妥催眠。虽然经卡拉胶处理的完整动物的睡眠时间延长了480%,但经卡拉胶处理的去睾丸大鼠的睡眠时间仅比对照动物长60%。然而,对切除睾丸的雄性大鼠进行睾丸切除或给予17 β -雌二醇,并没有抑制卡拉胶处理的单加氧酶活性。此外,给去卵巢的雌性大鼠注射睾酮并没有拮抗卡拉胶诱导的炎症的抑制作用。卡拉胶诱导的炎症对微粒体酶系统的抑制作用仅在成熟雄性大鼠中观察到,而在成熟雌性大鼠和性成熟大鼠中均未观察到。因此,这些结果表明,卡拉胶诱导的炎症对雄性大鼠肝脏9000 x g上清单加氧酶的抑制作用部分是通过卡拉胶诱导的炎症对该酶系统中雄激素依赖因子的毒性作用来介导的。
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Inhibition of hepatic drug biotransformation by carrageenan-induced inflammation in the rat: effect of sex hormone alterations.

Following in vivo treatment with carrageenan, sex-related differences in alteration of hepatic drug metabolism were found in the rat. In adult male rats, marked decreases were observed in hepatic 9000 x g supernatant cytochrome P-450 content and in the biotransformation of hexobarbital, aminopyrine, ethylmorphine, and meperidine. Hexobarbital hypnosis was significantly prolonged by carrageenan treatment in intact and testectomized animals as compared to their respective controls. Although carrageenan-treated intact animals slept 480% longer, carrageenan-treated testectomized rats slept only 60% longer than the respective control animals. However, testectomy or administration of 17 beta-estradiol to testectomized male rats did not inhibit the monooxygenase activities by carrageenan-treatment. Furthermore, administration of testosterone to ovariectomized female rats did not antagonize the inhibitory effects of the carrageenan-induced inflammation. The inhibitory effects produced by carrageenan-induced inflammation on the microsomal enzyme system were observed only in mature male rats and were not observed in mature female rats or in sexually immature rats of either sex. Thus, these results suggest that the inhibitory effects of carrageenan-induced inflammation on hepatic 9000 x g supernatant monooxygenases in the male rat are partially mediated through the toxic action of carrageenan-induced inflammation on androgen-dependent factors in this enzyme system.

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