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Curdione Plays an Important Role in the Inhibitory Effect ofCurcuma aromaticaon CYP3A4 in Caco-2 Cells
Author(s) -
Xiaolong Hou,
Emi Hayashi-Nakamura,
Tomoka TakataniNakase,
Ken Tanaka,
Kyôko Takahashi,
Katsuko Komatsu,
Koichi Takahashi
Publication year - 2010
Publication title -
evidence-based complementary and alternative medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.552
H-Index - 90
eISSN - 1741-4288
pISSN - 1741-427X
DOI - 10.1093/ecam/nep229
Subject(s) - inhibitory postsynaptic potential , cyp3a4 , curcuma , biology , traditional medicine , chemistry , endocrinology , medicine , botany , biochemistry , enzyme , cytochrome p450
Curcuma aromatica is a plant belonging to genus Curcuma of family Zingiberaceae and is widely used as supplements in Japan. Rhizomes of C. aromatica have curcumin as a major yellow pigment and curdione as a main ingredient of essential oils. In this study, we investigated the affect of C. aromatica on CYP3A4 using 1 α ,25-(OH) 2 -D 3 -treated Caco-2 clone cells. Caco-2 cells were treated with methanol extract (0.1 mg ml −1 ), its hexane soluble fraction (0.1 mg ml −1 ), curcumin (4  μ M) and curdione (20  μ M) for 72 hours. Nifedipine was used as a substrate of CYP3A4. Methanol extract, hexane fraction and curdione inhibited the formation of oxidized nifedipine by 50–70%, and curcumin showed no effect. The IC50s of methanol extract, hexane fraction and curdione to oxidized nifedipine formation were 21, 14 and 3.9  μ g ml −1 (16.9  μ M), respectively. The content of curdione in methanol extract was 11.4%. Moreover, all of methanol extract, hexane fraction and curdione decreased CYP3A4 protein expression but had no affect on CYP3A4 mRNA expression. Our results showed that these drugs further decreased the CYP3A4 protein expression level after the protein synthesis was inhibited by cychroheximide. These findings suggest that curdione plays an important role in the CYP3A4 inhibitory activity of C. aromatica and curdione might inhibit the activity by accelerating the degradation of CYP3A4.

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