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2015 Fiscal Year Final Research Report

Development of noninvasive drug metabolizing enzyme activity estimate method for side effect reduction of the drugs

Research Project

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Project/Area Number 25670077
Research Category

Grant-in-Aid for Challenging Exploratory Research

Allocation TypeMulti-year Fund
Research Field Medical pharmacy
Research InstitutionOsaka Kyoiku University

Principal Investigator

Katagiri Masanao  大阪教育大学, 教育学部, 教授 (00185802)

Project Period (FY) 2013-04-01 – 2016-03-31
Keywordsステロイド代謝 / 薬物代謝 / CYP3A4 / リアーゼ活性
Outline of Final Research Achievements

Fourteen CYPs which are drug metabolizing enzymes in human liver were reacted to more than eight kinds of adrenal steroids and their metabolites were identified. As a result, only CYP3A4 showed a various metabolite on HPLC chart. Production of androstendion from 17alpha-hydroxyprogesterone and 11-deoxycortisol by CYP3A4 was confirmed by GC-MS. It was revealed that CYP3A4 can catalyze side chain cleavage reaction (Lyase activity) to the steroids. 6beta-Hydoxy metabolite which were main metabolite from 11-deoxycortisol was identified. Then, Km and Vmax of 6beta-hydroxylase activity and Lyase activity against 11-deoxycortisol were determined and compared.

Free Research Field

ステロイド代謝

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Published: 2017-05-10  

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