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  1. C. 医薬保健学域; 医学類・薬学類・医薬科学類・保健学類
  2. c 10. 学術雑誌掲載論文(医・保健)
  3. 2.査読済論文(薬)

Utilization of Liver Microsomes to Estimate Hepatic Intrinsic Clearance of Monoamine Oxidase Substrate Drugs in Humans

http://hdl.handle.net/2297/47882
http://hdl.handle.net/2297/47882
57f23762-8f3f-46c2-9fea-963fb2298968
名前 / ファイル ライセンス アクション
PH-PR-KATO-Y-1233.pdf PH-PR-KATO-Y-1233.pdf (259.1 kB)
Item type 学術雑誌論文 / Journal Article(1)
公開日 2017-12-05
タイトル
タイトル Utilization of Liver Microsomes to Estimate Hepatic Intrinsic Clearance of Monoamine Oxidase Substrate Drugs in Humans
言語
言語 eng
資源タイプ
資源タイプ識別子 http://purl.org/coar/resource_type/c_6501
資源タイプ journal article
著者 Masuo, Yusuke

× Masuo, Yusuke

WEKO 580
e-Rad 90708140
金沢大学研究者情報 90708140
研究者番号 90708140

Masuo, Yusuke

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Nagamori, Shushi

× Nagamori, Shushi

WEKO 68968

Nagamori, Shushi

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Hasegawa, Aoi

× Hasegawa, Aoi

WEKO 68969

Hasegawa, Aoi

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Hayashi, Kazuki

× Hayashi, Kazuki

WEKO 68970

Hayashi, Kazuki

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Isozumi, Noriyoshi

× Isozumi, Noriyoshi

WEKO 68971

Isozumi, Noriyoshi

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Nakamichi, Noritaka

× Nakamichi, Noritaka

WEKO 293
e-Rad 10401895
金沢大学研究者情報 10401895
研究者番号 10401895

Nakamichi, Noritaka

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Kanai, Yoshikatsu

× Kanai, Yoshikatsu

WEKO 68972

Kanai, Yoshikatsu

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Kato, Yukio

× Kato, Yukio

WEKO 29
e-Rad 30251440
金沢大学研究者情報 30251440
研究者番号 30251440

Kato, Yukio

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書誌情報 Pharmaceutical Research

巻 34, 号 6, p. 1233-1243, 発行日 2017-06-01
ISSN
収録物識別子タイプ ISSN
収録物識別子 0724-8741
NCID
収録物識別子タイプ NCID
収録物識別子 AA10632083
DOI
関連タイプ isVersionOf
識別子タイプ DOI
関連識別子 10.1007/s11095-017-2140-4
出版者
出版者 Springer
抄録
内容記述タイプ Abstract
内容記述 Purpose: Monoamine oxidases (MAOs) are non-CYP enzymes that contribute to systemic elimination of therapeutic agents, and localized on mitochondrial membranes. The aim of the present study was to validate quantitative estimation of metabolic clearance of MAO substrate drugs using human liver microsomes (HLMs). Methods: Three MAO substrate drugs, sumatriptan, rizatriptan and phenylephrine, as well as four CYP substrates were selected, and their disappearance during incubation with HLMs or mitochondria (HLMt) was measured. Metabolic clearance (CL) was then calculated from the disappearance curve. Results: CL obtained in HLMs for sumatriptan and a typical MAO substrate serotonin was correlated with that obtained in HLMt among ten human individual livers. Hepatic intrinsic clearance (CLint,vitro) estimated from CL in HLMs was 14–20 and 2–5 times lower than in vivo hepatic intrinsic clearance (CLint,vivo) obtained from literature for MAO and CYP substrates, respectively. Utilization of HLMs for quantitatively assessing metabolic clearance of MAO substrates was further validated by proteomics approach which has revealed that numerous proteins localized on inner and outer membranes of mitochondria were detected in both HLMs and HLMt. Conclusion: CLint,vitro values of MAO substrate drugs can be quantitatively estimated with HLMs and could be used for semi-quantitative prediction of CLint,vivo values. © 2017 Springer Science+Business Media New York
内容記述
内容記述タイプ Other
内容記述 Embargo Period 12 months
権利
権利情報 © 2017 Springer Science+Business Media New York | The final publication is available at www.springerlink.com/article/10.1007/s11095-017-2140-4
著者版フラグ
出版タイプ AM
出版タイプResource http://purl.org/coar/version/c_ab4af688f83e57aa
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