Identification of Human P450 Isoforms Involved in the Metabolism of the Antiallergic Drug, Oxatomide, and Its Kinetic Parameters and Inhibition Constants(Miscellaneous)
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概要
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Oxatomide is an antiallergic drug used for the treatment of diseases mediated by type I allergy. Recently, terfenadine and astemizole, which have antiallergic actions similar to those of oxatomide, showed side effects on the cardiovascular system. This might be because concomitant drugs such as itraconazole inhibit cytochrome P450 3A4 (CYP3A4), the enzyme responsible for the degradation of terfenadine and astemizole, and thus the blood concentrations of the drugs are abnormally increased. In another article of this issue, we have reported that oxatomide is metabolized by CYP2D6-Val and CYP3A4, and simultaneously inhibits the metabolism of the model substrates for these enzymes. In this study, we performed the kinetic analysis of oxatomide metabolism using microsomes prepared from human liver, and found that the K_m and V_<max> values were 26.1μм and 1254.4 pmol/mg protein/min, respectively. Ketoconazole, one of the representative inhibitors for CYP3A4, potently inhibited the metabolism of oxatomide, but other well-known CYP inhibitors did not show significant inhibition. These results suggest that the metabolism of oxatomide is principally catalyzed by CYP3A4. Furthermore, oxatomide inhibited the metabolism of (±) bufuralol and testosterone, model substrates for CYP2D6 and CYP3A4, respectively, in a dose-dependent manner with the K_i values of 57.4 and 24.3μм, respectively. These observations, together with the finding that the putative highest concentration of oxatomide in blood was ≅40 ng/ml (≅93 nм) at 4 h after each dosage during consecutive 6-d administration, encouraged us to conclude that oxatomide won't inhibit CYP2D6 or CYP3A4 at clinical doses.
- 公益社団法人日本薬学会の論文
- 2005-02-01
著者
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KOBAYASHI Hiroyuki
Pharmaceutical Research Center, Kyowa Hakko Kogyo Co., Ltd.
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Sakai K
Yaizu Suisan Kagaku Ind. Co. Yaizu Jpn
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Sakai Kenichi
Department Of Mathematical And Life Sciences Graduate School Of Science Hiroshima University
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Nakajima Hiroshi
Department Of Earth And Space Science Osaka University
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Horikoshi K
Drug Development Research Laboratories Pharmaceutical Research Institute Kyowa Kogyo Co. Ltd.
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Kobayashi H
Department Of Earth & Spece Science Graduate School Of Science Osaka University
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Inaba Atsuhiro
Adme And Tox Research Institute Daiichi Pure Chemicals Co. Ltd.
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GOTO Akihisa
Pharmaceutical Research Institute, Kyowa Hakko Kogyo Co., Ltd.
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NAKAJIMA Hiroshi
Pharmaceutical Research Institute, Kyowa Hakko Kogyo Co., Ltd.
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UEDA Koji
ADME and TOX Research Institute, Daiichi Pure Chemicals Co., Ltd.
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Ueda Koji
Adme And Tox Research Institute Daiichi Pure Chemicals Co. Ltd.
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Goto Akihisa
Pharmaceutical Research Institute Kyowa Hakko Kogyo Co. Ltd.
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Kobayashi H
Pharmaceutical Research Institute Kyowa Hakko Kogyo Co. Ltd.
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Kobayashi Hiroyuki
Pharmaceutical Research Center Kyowa Hakko Kogyo Co. Ltd.
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Nakajima H
Department Of Earth And Space Science Osaka University
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Nakajima Hiroshi
Department of Physics, Nihon University
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NAKAJIMA Hiroshi
Department of Physics, Kyoto University
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NAKAJIMA Hiroshi
Department of Physics, Science University of Tokyo
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Horikoshi Kaori
Pharmaceutical Research Institute, Kyowa Hakko Kogyo Co., Ltd.
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