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利福平对比格犬肠道细胞色素P450(CYP3A)的诱导作用。

Induction of intestinal cytochrome P450 (CYP3A) by rifampicin in beagle dogs.

作者信息

Kyokawa Y, Nishibe Y, Wakabayashi M, Harauchi T, Maruyama T, Baba T, Ohno K

机构信息

Developmental Research Laboratories, Shionogi & Co. Ltd., 3-1-1 Futaba-cho, Toyonaka, 561-0825, Osaka, Japan

出版信息

Chem Biol Interact. 2001 May 16;134(3):291-305. doi: 10.1016/s0009-2797(01)00164-8.

Abstract

Both male and female beagle dogs (four dogs/sex) were orally treated with rifampicin (Rif) at the dose of 10 mg/kg/day for 7 days and an additional eight dogs (four dogs/sex) were used as a control. The inducible effect of Rif on intestinal cytochrome P450, especially CYP3A enzyme, was investigated by measuring microsomal testosterone 6beta-hydroxylation (6beta-OHT) activity, immunoblot and ELISA analysis. In male dogs, microsomal 6beta-OHT activity in the duodenum, upper, middle and lower part of the jejunum and the ileum of the control was 229, 204, 194, 129 and 57 pmol/min/mg protein, while the activity of the Rif-treated dogs significantly increased to 456, 486, 430, 192 and 138 pmol/min/mg protein, respectively. The activity of intestinal 6beta-OHT in the control and Rif-treated female dogs showed almost similar levels to those observed in the corresponding male dogs. The activity of intestinal 6beta-OHT in both control and Rif-treated dogs was specifically inhibited by anti-CYP3A12 antiserum. The apparent K(m) value for 6beta-OHT activity in all sections of the small intestine was comparable with that in the liver, and no significant changes were observed in between control and Rif-treated dogs. In both control and Rif-treated dogs, immunoblotting of intestinal microsomes with anti-CYP3A12 antiserum produced a band indistinguishable from that of purified CYP3A12 or of immunoreactive CYP3A12 in liver microsomes. A significant increase in intestinal CYP3A content by Rif treatment was quantitatively verified by the ELISA analysis and the magnitude of its increase correlated well with that of 6beta-OHT activity elevation. Furthermore, the results of immunohistochemistry using the anti-CYP3A12 antiserum indicated that CYP3A protein was specifically distributed in epithelial cells throughout the small intestine and appeared to be predominant at the apical side of villus cells. These results demonstrate that Rif induces not only hepatic CYP3A12 but also intestinal CYP3A in dogs.

摘要

雄性和雌性比格犬(每种性别各4只)口服利福平(Rif),剂量为10mg/kg/天,持续7天,另外8只犬(每种性别各4只)作为对照。通过测量微粒体睾酮6β-羟化(6β-OHT)活性、免疫印迹和ELISA分析,研究利福平对肠道细胞色素P450,尤其是CYP3A酶的诱导作用。在雄性犬中,对照组十二指肠、空肠上、中、下部分和回肠的微粒体6β-OHT活性分别为229、204、194、129和57pmol/min/mg蛋白,而利福平处理组犬的活性分别显著增加至456、486、430、192和138pmol/min/mg蛋白。对照组和利福平处理组雌性犬的肠道6β-OHT活性与相应雄性犬的水平几乎相似。对照组和利福平处理组犬的肠道6β-OHT活性均被抗CYP3A12抗血清特异性抑制。小肠各段6β-OHT活性的表观K(m)值与肝脏中的相当,对照组和利福平处理组犬之间未观察到显著变化。在对照组和利福平处理组犬中,用抗CYP3A12抗血清对肠道微粒体进行免疫印迹产生的条带与纯化的CYP3A12或肝脏微粒体中免疫反应性CYP3A12的条带无法区分。ELISA分析定量证实利福平处理后肠道CYP3A含量显著增加,其增加幅度与6β-OHT活性升高幅度密切相关。此外,使用抗CYP3A12抗血清的免疫组织化学结果表明,CYP3A蛋白特异性分布于整个小肠的上皮细胞中,并且似乎在绒毛细胞的顶端侧占主导。这些结果表明,利福平不仅诱导犬肝脏中的CYP3A12,还诱导肠道中的CYP3A。

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