TY - JOUR
T1 - Curdione plays an important role in the inhibitory effect of curcuma aromatica on CYP3A4 in Caco-2 cells
AU - Hou, Xiao Long
AU - Hayashi-Nakamura, Emi
AU - Takatani-Nakase, Tomoka
AU - Tanaka, Ken
AU - Takahashi, Kyoko
AU - Komatsu, Katsuko
AU - Takahashi, Koichi
PY - 2011
Y1 - 2011
N2 - 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 1,25-(OH)2-D3-treated Caco-2 clone cells. Caco-2 cells were treated with methanol extract (0.1mgml-1), its hexane soluble fraction (0.1mgml-1), curcumin (4M) and curdione (20M) for 72 hours. Nifedipine was used as a substrate of CYP3A4. Methanol extract, hexane fraction and curdione inhibited the formation of oxidized nifedipine by 5070, and curcumin showed no effect. The IC50s of methanol extract, hexane fraction and curdione to oxidized nifedipine formation were 21, 14 and 3.9gml- (16.9M), 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.
AB - 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 1,25-(OH)2-D3-treated Caco-2 clone cells. Caco-2 cells were treated with methanol extract (0.1mgml-1), its hexane soluble fraction (0.1mgml-1), curcumin (4M) and curdione (20M) for 72 hours. Nifedipine was used as a substrate of CYP3A4. Methanol extract, hexane fraction and curdione inhibited the formation of oxidized nifedipine by 5070, and curcumin showed no effect. The IC50s of methanol extract, hexane fraction and curdione to oxidized nifedipine formation were 21, 14 and 3.9gml- (16.9M), 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.
UR - http://www.scopus.com/inward/record.url?scp=79955094886&partnerID=8YFLogxK
U2 - 10.1093/ecam/nep229
DO - 10.1093/ecam/nep229
M3 - 学術論文
C2 - 21785639
AN - SCOPUS:79955094886
SN - 1741-427X
VL - 2011
JO - Evidence-based Complementary and Alternative Medicine
JF - Evidence-based Complementary and Alternative Medicine
M1 - 913898
ER -