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小花山柰提取物及其黄酮成分对P-糖蛋白功能的影响。

Effects of Kaempferia parviflora extracts and their flavone constituents on P-glycoprotein function.

作者信息

Patanasethanont Denpong, Nagai Junya, Yumoto Ryoko, Murakami Teruo, Sutthanut Khaetthareeya, Sripanidkulchai Bung-Orn, Yenjai Chavi, Takano Mikihisa

机构信息

Department of Pharmaceutics and Therapeutics, Graduate School of Biomedical Sciences, Hiroshima University, 1-2-3 Kasumi, Hiroshima 734-8553, Japan.

出版信息

J Pharm Sci. 2007 Jan;96(1):223-33. doi: 10.1002/jps.20769.

Abstract

The purpose of this study was to examine the effects of extracts and flavone derivatives from the rhizome of Kaempferia parviflora on P-glycoprotein (P-gp)-mediated transport in LLC-GA5-COL150, a transfectant cell line of a porcine kidney epithelial cell line LLC-PK1 with human MDR1 cDNA. Ethanol extract obtained from Kaempferia parviflora rhizome significantly increased the accumulation of rhodamine 123 and daunorubicin, P-gp substrates, in LLC-GA5-COL150 cells, but not in LLC-PK1 cells. The aqueous extract also increased the accumulation in LLC-GA5-COL150 cells with lower potency than the ethanol extract. The effects of flavone derivatives isolated from the rhizome of Kaempferia parviflora on P-gp function were examined. Among six flavones tested, 3,5,7,3',4'-pentamethoxyflavone most potently increased the accumulation of rhodamine 123 and daunorubicin in LLC-GA5-COL150 cells in a concentration-dependent manner. In addition, 5,7-dimethoxyflavone to lesser degree increased rhodamine 123 accumulation in LLC-GA5-COL150 cells. In contrast, the other four flavone derivatives had no significant effect on the accumulation of rhodamine 123 in LLC-GA5-COL150 cells in a concentration range tested. These results indicate that extracts and flavone derivatives from the rhizome of Kaempferia parviflora can inhibit P-gp function, which may be useful for overcoming P-gp-mediated multidrug resistance and improving the oral bioavailability of anticancer agents.

摘要

本研究旨在考察小花山柰根茎提取物及黄酮衍生物对LLC-GA5-COL150细胞中P-糖蛋白(P-gp)介导转运的影响,LLC-GA5-COL150是转染了人MDR1 cDNA的猪肾上皮细胞系LLC-PK1的细胞系。从小花山柰根茎中获得的乙醇提取物显著增加了LLC-GA5-COL150细胞中P-gp底物罗丹明123和柔红霉素的蓄积,但对LLC-PK1细胞无此作用。水提取物也增加了LLC-GA5-COL150细胞中的蓄积,但其效力低于乙醇提取物。考察了从小花山柰根茎中分离得到的黄酮衍生物对P-gp功能的影响。在所测试的六种黄酮中,3,5,7,3',4'-五甲氧基黄酮最有效地以浓度依赖性方式增加了LLC-GA5-COL150细胞中罗丹明123和柔红霉素的蓄积。此外,5,7-二甲氧基黄酮在较小程度上增加了LLC-GA5-COL150细胞中罗丹明123的蓄积。相反,在测试的浓度范围内,其他四种黄酮衍生物对LLC-GA5-COL150细胞中罗丹明123的蓄积无显著影响。这些结果表明,小花山柰根茎提取物及黄酮衍生物可抑制P-gp功能,这可能有助于克服P-gp介导的多药耐药性并提高抗癌药物的口服生物利用度。

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