Metabolism of OR-1896, a metabolite of levosimendan, in rats and humans

被引:4
作者
Koskinen, M. [1 ]
Puttonen, J. [2 ,3 ]
Pykalainen, M. [1 ]
Vuorela, A. [1 ]
Lotta, T. [1 ]
机构
[1] Orion Corp Orion Pharma, R&D, Dept Pharmacokinet & Bioanal, FIN-02101 Espoo, Finland
[2] Orion Pharma, R&D, Clin R&D, Kuopio, Finland
[3] Univ Kuopio, Dept Pharmaceut, Kuopio, Finland
关键词
D O I
10.1080/00498250701744658
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
OR-1896 is a pharmacologically active, long-lived metabolite of levosimendan. In the current study, the metabolism of C-14-labelled OR-1896 was investigated in six healthy men after intravenous infusion over 10 min and in male rats after an intravenous bolus dose. In human plasma, the only 14C-compounds detected were C-14-OR-1896 and its deacetylated form, C-14-OR-1855, in varying proportions in different subjects. In rat plasma 93% of radioactivity was associated with OR-1896. Radioactivity was mainly excreted to urine in both rats (about 69% of the dose) and humans (about 87% of the dose). OR-1896 was a major urinary compound in both humans and rats. Another major human metabolite was hypothesized as N-conjugated OR-1855. Other human and rat urinary biotransformation products were characterized as N-hydroxylated OR-1896 and N-hydroxylated OR-1855, as well as glucuronide or sulphate conjugates of N-hydroxyl OR-1896. The main difference between rat and human metabolism was a lower amount of OR-1855-related metabolites in the rats. In human faecal homogenates, only OR-1896 and OR-1855 were detected, whereas rat faecal metabolite profile was similar to that in urine.
引用
收藏
页码:156 / 170
页数:15
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