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莪术二酮在莪术醇抑制 Caco-2 细胞 CYP3A4 中的作用

Curdione Plays an Important Role in the Inhibitory Effect of Curcuma aromatica on CYP3A4 in Caco-2 Cells.

机构信息

Department of Pharmaceutics, School of Pharmaceutical Sciences, Mukogawa Women's University, 9-11-68 koushien, Nishinomiya City, Hyogo, Japan.

出版信息

Evid Based Complement Alternat Med. 2011;2011:913898. doi: 10.1093/ecam/nep229. Epub 2011 Mar 13.

Abstract

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 1α,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 μM) and curdione (20 μM) 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 μg ml(-1) (16.9 μM), 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.

摘要

姜黄是姜科姜黄属植物,在日本被广泛用作补充剂。姜黄根茎中的主要黄色素为姜黄素,主要精油成分为莪术二酮。在本研究中,我们使用 1α,25-(OH)(2)-D(3)处理的 Caco-2 克隆细胞,研究了姜黄对 CYP3A4 的影响。Caco-2 细胞用甲醇提取物(0.1mg/ml)、其正己烷可溶部分(0.1mg/ml)、姜黄素(4μM)和莪术二酮(20μM)处理 72 小时。硝苯地平用作 CYP3A4 的底物。甲醇提取物、正己烷部分和莪术二酮抑制氧化硝苯地平的形成达 50-70%,而姜黄素则没有效果。甲醇提取物、正己烷部分和莪术二酮对氧化硝苯地平形成的 IC50 分别为 21、14 和 3.9μg/ml(16.9μM)。甲醇提取物中莪术二酮的含量为 11.4%。此外,甲醇提取物、正己烷部分和莪术二酮均降低 CYP3A4 蛋白表达,但对 CYP3A4 mRNA 表达无影响。我们的结果表明,在细胞松弛素 B 抑制蛋白合成后,所有这些药物进一步降低了 CYP3A4 蛋白表达水平。这些发现表明,莪术二酮在姜黄对 CYP3A4 的抑制活性中起着重要作用,莪术二酮可能通过加速 CYP3A4 的降解来抑制其活性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5cf9/3137788/0ced4772ccba/ECAM2011-913898.001.jpg

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