Proceedings of the Korean Society of Toxicology Conference (한국독성학회:학술대회논문집)
- 2001.10a
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- Pages.195-195
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- 2001
IN VITRO INHIBITION BY TRICYCLIC ANTIDEPRESSANTS OF PHENYTOIN p-HYDROXYLATION: MECHANISTIC APPROACH
- Park, Ji-Young (Dept. of Phannacol., Inje Univ., ColI. of Med. and Clin. Phannacol. Center, Pusan Paik Hosp.) ;
- Kim, Min-Jung (Dept. of Phannacol., Coll. of Med) ;
- Shon, Ji-Hong (Dept. of Phannacol., Coll. of Med) ;
- Shin, Jae-Gook (Dept. of Phannacol., Coll. of Med.)
- Published : 2001.10.01
Abstract
The inhibitory potentials of TCAs (imipramine, desipramine, amitriptyline, and nortriptyline) on phenytoin p-hydroxylation and probe metabolic pathways of each CYP isoforms were evaluated from incubation studies of human liver microsomes and cDNA-expressed cytochrome P450s in vitro in order to understand the mechanism of drug interaction between TCAs and phenytoin, a substrate of CYP2C9 and CYP2C19. (omitted)
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