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人肝细胞移植的嵌合型TK-NOG小鼠对去氯雷他定的代谢

Metabolism of desloratadine by chimeric TK-NOG mice transplanted with human hepatocytes.

作者信息

Uehara Shotaro, Yoneda Nao, Higuchi Yuichiro, Yamazaki Hiroshi, Suemizu Hiroshi

机构信息

Central Institute for Experimental Animals, Kawasaki, Japan.

Laboratory of Drug Metabolism and Pharmacokinetics, Showa Pharmaceutical University, Machida, Japan.

出版信息

Xenobiotica. 2020 Jun;50(6):733-740. doi: 10.1080/00498254.2019.1688892. Epub 2019 Nov 12.

Abstract
  1. Desloratadine is an antiallergic drug with species-dependent metabolic profiles in mice, rats, monkeys and humans. We investigated whether humanized-liver mice could reproduce the reported human-specific metabolic profile for desloratadine in terms of the formation of 3-hydroxydesloratadine and its -glucuronide.2. Hepatocytes prepared from humans and humanized-liver mice both preferentially catalyzed the formation of 3-hydroxydesloratadine and its -glucuronide .3. After a single oral administration of desloratadine, plasma levels of desloratadine and its metabolites (3-hydroxydesloratadine and its -glucuronide) in humanized-liver mice were lower and higher, respectively, than those in control mice.4. The amounts of 3-hydroxydesloratadine and its -glucuronide excreted in humanized-liver mouse feces and urine were higher than those of the control mice, whereas 5- and 6-hydroxydesloratadine formation were predominant in the feces and urine samples from control mice. A significant correlation ( = 0.68) for the dose percentage of urinary and fecal metabolites of desloratadine was only observed between the humanized-liver mice and the reported values for humans.5. These results indicated that urinary 3-hydroxydesloratadine -glucuronide and fecal desloratadine, 3-hydroxydesloratadine and 5-hydroxydesloratadine were the major excretion pathways of desloratadine in humanized-liver mice, which is reasonably similar to that reported for humans.
摘要
  1. 地氯雷他定是一种抗过敏药物,在小鼠、大鼠、猴子和人类中具有物种依赖性代谢特征。我们研究了人源化肝脏小鼠是否能够在3-羟基地氯雷他定及其葡萄糖醛酸苷的形成方面重现报道的地氯雷他定的人类特异性代谢特征。

  2. 从人类和人源化肝脏小鼠制备的肝细胞均优先催化3-羟基地氯雷他定及其葡萄糖醛酸苷的形成。

  3. 单次口服地氯雷他定后,人源化肝脏小鼠血浆中的地氯雷他定及其代谢产物(3-羟基地氯雷他定及其葡萄糖醛酸苷)水平分别低于和高于对照小鼠。

  4. 人源化肝脏小鼠粪便和尿液中排泄的3-羟基地氯雷他定及其葡萄糖醛酸苷的量高于对照小鼠,而对照小鼠粪便和尿液样本中5-羟基地氯雷他定和6-羟基地氯雷他定的形成占主导。仅在人源化肝脏小鼠与报道的人类值之间观察到地氯雷他定尿和粪便代谢产物剂量百分比的显著相关性(r = 0.68)。

  5. 这些结果表明,尿中3-羟基地氯雷他定葡萄糖醛酸苷和粪便中的地氯雷他定、3-羟基地氯雷他定和5-羟基地氯雷他定是人源化肝脏小鼠中地氯雷他定的主要排泄途径,这与报道的人类排泄途径合理相似。

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