Metabolic activation of 1α-hydroxyvitamin D3 in human liver microsomes

被引:8
作者
Kamachi, S
Sugimoto, K
Yamasaki, T
Hirose, N
Ide, H
Ohyama, Y [1 ]
机构
[1] Hiroshima Univ, Grad Sch Sci, Dept Math & Life Sci, Higashihiroshima 7398526, Japan
[2] Chugai Pharmaceut Co Ltd, Prod Res Lab, Toshima Ku, Tokyo 1718545, Japan
[3] Panapharm Labs Co Ltd, Pharmacokinet, Kumamoto 8690425, Japan
关键词
D O I
10.1080/00498250110057369
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
1. 1 alpha -Hydroxyvitamin D-3 (1 alpha -OH-D-3) is a synthetic prodrug of the active form of vitamin D-3, and requires the hydroxylation at the C-25 position before eliciting its biological activity. 2. 25-Hydroxylation activities for 1 alpha -OH-D-3 were present in both microsomal and mitochondrial fractions of human liver. 3. To determine the P450 enzyme(s) involved in microsomal 25-hydroxylation, 14 P450s (CYP1A1, 1A2, 1B1, 2A6, 2B6, 2C8, 2C9-Arg, 2C9-Cys, 2C19, 2D6-Val, 2D6-Met, 2E1, 3A4, 4A11) were tested for their 25-hydroxylation activity of 1 alpha -OH-D-3. None catalysed the 25-hydroxylation reaction. 4. 1 alpha -OH-D-3 in a high concentration (2.5 ng ml(-1)) showed small but significant inhibition of the catalytic activities of CYP2C8, 2C9-Cys, 2C19, 2D6-Val and 2E1 for their typical substrates. However, 1 alpha -OH-D-3 in a clinically used low concentration will not significantly affect drug metabolism catalysed by the 14 P450s tested. 5. In summary, the 25-hydroxylation activity of 1 alpha -OH-D-3 that localizes in the microsomal fraction appears to be attributable to a cytochrome P450 other than the microsomal forms tested in this study.
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页码:701 / 712
页数:12
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