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2018 Fiscal Year Final Research Report

CYP-Mediated Metabolism and Toxicity of Dangerous Drugs, Synthetic Cannabinoids,

Research Project

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Project/Area Number 16K08354
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeMulti-year Fund
Section一般
Research Field Environmental and hygienic pharmacy
Research InstitutionDaiichi University, College of Pharmaceutical Sciences

Principal Investigator

WATANABE KAZUHITO  第一薬科大学, 薬学部, 教授 (30113038)

Project Period (FY) 2016-04-01 – 2019-03-31
Keywords危険ドラッグ / HU-210 / HU-211 / 代謝 / 細胞毒性 / シトクロムP450 / CYP発現系
Outline of Final Research Achievements

1)Among 13 synthetic cannabinoids examined, JWH-018, JWH-073, JWH-133, AM251, SR144,528, Rimonabant, delta-9,11-THC, HU-210 and HU-211 exhibited Type I spectra with human liver microsomal cytochrome P450 (CYP).2)Delta-9,11-THC showed more potent cytotoxic effect to MCF-7 cell compared to delta-9-THC.3)HLMs metabolism of HU-210role andHU-211 was studied, and important role of CYP3A4 was clarified.4)Synthetic cannabinoids, JWH-018、JWH-073、HU-211、WIN-55212-1 and WIN-55212-2 induced differentiation of 3T3-L1 cell to adipocyte cells.

Free Research Field

衛生薬学

Academic Significance and Societal Importance of the Research Achievements

本研究で得られた成果は、合成CB受容体アゴニスト(特にJWH-018, JWH-073, HU-210など)のヒトカンミクロソームによる代謝を明らかにしたものであり、関与するCYP分子種の情報や細胞毒性も含めて、薬物相互作用や薬理毒性などの健康被害を考える上で有用な基礎的な知見を与える学術的意義がある。また、代謝の情報は関連薬物を生体試料から検出する際に極めて重要であり、社会的意義を有するものと考えられる。

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Published: 2020-03-30  

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