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用微粒体酶诱导剂预处理后黄曲霉毒素P1葡糖醛酸结合作用增加。

Increase in glucuronide conjugation of aflatoxin P1 after pretreatment with microsomal enzyme inducers.

作者信息

Ehrich M, Huckle W R, Larsen C

出版信息

Toxicology. 1984 Aug;32(2):145-52. doi: 10.1016/0300-483x(84)90133-1.

Abstract

Microsomes prepared from livers of chickens given enzyme inducers had increased capability to convert aflatoxin P1 to its glucuronide conjugate. This capability was 190% +/- 19 and 184% +/- 13 of control values (mean +/- S.E., N = 4) 96 h after intraperitoneal administration of 80 mg/kg beta-naphthoflavone or 3-methylcholanthrene, respectively. Glucuronidation of aflatoxin P1 was also increased 15 days after 500 mg/kg i.p. of a polychlorinated biphenyl mixture (to 471% +/- 111). Fifteen days on a low protein diet (containing 54% of normal levels) did not alter aflatoxin glucuronidation. Increased glucuronidation after administration of inducers was due to increased specific activity of the microsomal enzymes.

摘要

用酶诱导剂处理过的鸡肝脏制备的微粒体,将黄曲霉毒素P1转化为其葡萄糖醛酸共轭物的能力增强。腹腔注射80mg/kgβ-萘黄酮或3-甲基胆蒽96小时后,这种能力分别为对照值的190%±19和184%±13(平均值±标准误,N = 4)。腹腔注射500mg/kg多氯联苯混合物15天后,黄曲霉毒素P1的葡萄糖醛酸化也增加(至471%±111)。低蛋白饮食(含正常水平的54%)15天并未改变黄曲霉毒素的葡萄糖醛酸化。诱导剂给药后葡萄糖醛酸化增加是由于微粒体酶的比活性增加。

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