Gewirtz D A, Yanovich S
Biochem Pharmacol. 1987 Jun 1;36(11):1793-8. doi: 10.1016/0006-2952(87)90240-1.
Metabolism of adriamycin, an anthracycline antibiotic, was characterized in both rat and rabbit hepatocytes under aerobic conditions. Adriamycin was the predominant fluorescent species within the cell in hepatocytes from both the rat and the rabbit. In the rat hepatocyte, the primary intracellular metabolite was deoxyadriamycin aglycone, while significant levels of deoxyadriamycinol aglycone were also synthesized; little adriamycinol was observed in the cells or the incubation medium. In contrast, in the rabbit hepatocyte, significant levels of adriamycinol as well as deoxyadriamycinol aglycone were formed; deoxyadriamycinol aglycone was the primary intracellular metabolite while low levels of deoxyadriamycin aglycone were observed. The relative formation of deoxyadriamycinol aglycone and deoxyadriamycin aglycone suggests that adriamycinol may be metabolized more effectively to the deoxyaglycone derivative than the parent drug. Conjugates of adriamycin were not observed in hepatocytes from either the rat or the rabbit or in the incubation medium.
在有氧条件下,对大鼠和兔肝细胞中蒽环类抗生素阿霉素的代谢进行了表征。阿霉素是大鼠和兔肝细胞内主要的荧光物质。在大鼠肝细胞中,主要的细胞内代谢产物是脱氧阿霉素苷元,同时也合成了大量的脱氧阿霉素醇苷元;在细胞或孵育培养基中观察到的阿霉素醇很少。相比之下,在兔肝细胞中,形成了大量的阿霉素醇以及脱氧阿霉素醇苷元;脱氧阿霉素醇苷元是主要的细胞内代谢产物,而观察到的脱氧阿霉素苷元水平较低。脱氧阿霉素醇苷元和脱氧阿霉素苷元的相对形成表明,与母体药物相比,阿霉素醇可能更有效地代谢为脱氧苷元衍生物。在大鼠或兔的肝细胞以及孵育培养基中均未观察到阿霉素的缀合物。