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小花山柰化合物的抗过敏活性。

Anti-allergic activity of compounds from Kaempferia parviflora.

作者信息

Tewtrakul Supinya, Subhadhirasakul Sanan, Kummee Sopa

机构信息

Department of Pharmacognosy and Pharmaceutical Botany, Faculty of Pharmaceutical Sciences, Prince of Songkla University, Hat-Yai, Songkhla 90112, Thailand.

出版信息

J Ethnopharmacol. 2008 Feb 28;116(1):191-3. doi: 10.1016/j.jep.2007.10.042. Epub 2007 Nov 6.

Abstract

Kaempferia parviflora is one of the plants in the Zingiberaceae family, locally known in Thai as kra-chai-dam. In Thai traditional medicine, the decoction of Kaempferia parviflora powder with alcohol has been reported to cure allergy, asthma, impotence, gout, diarrhea, dysentery, peptic ulcer and diabetes. Therefore, the present study aimed to investigate anti-allergic substances from this plant. Bioassay-guided fractionation led to the isolation of seven methoxyflavone derivatives (1-7) from Kaempferia parviflora extract and they were identified on the basis of spectroscopic methods. Among the compounds tested, 5-hydroxy-3,7,3',4'-tetramethoxyflavone (5) possessed the highest anti-allergic activity against antigen-induced beta-hexosaminidase release as a marker of degranulation in RBL-2H3 cells with an IC(50) value of 8.0 microM, followed by 5-hydroxy-7-methoxyflavone (2, IC(50)=20.6 microM) and 5-hydroxy-7,4'-dimethoxyflavone (4, IC(50)=26.0 microM), whereas others showed moderate activities (IC(50)=37.5-66.5 microM). Structure-activity trends of 7-methoxyflavone derivatives on anti-allergic activity can be summarized as follows: (1) substitution with vicinal methoxyl groups at positions 3' and 4' conferred higher activity than only one methoxylation, (2) methoxylation at position 3 reduced activity and (3) methoxylation at position 5 showed higher activity than hydroxylation. Compounds 2, 4 and 5 were also determined for their mechanisms on ionomycin-induced beta-hexosaminidase release. The results indicated that the mechanism on inhibition of cell degranulation of compounds 2 and 5 mainly involve the inhibition of Ca(2+) influx to the cells, whereas that of 4 may be partly due to this inhibition. In regards to the active constituents for anti-allergic activity of Kaempferia parviflora, 5-hydroxy-3,7,3',4'-tetramethoxyflavone (5), 5-hydroxy-7-methoxyflavone (2) and 5-hydroxy-7,4'-dimethoxyflavone (4) are responsible for anti-allergic effect of this plant. The findings support the traditional use of Kaempferia parviflora rhizomes for treatment of allergy and allergy-related diseases.

摘要

小花山柰是姜科植物之一,在泰国当地被称为kra-chai-dam。在泰国传统医学中,据报道小花山柰粉末与酒精的煎剂可治疗过敏、哮喘、阳痿、痛风、腹泻、痢疾、消化性溃疡和糖尿病。因此,本研究旨在研究该植物中的抗过敏物质。通过生物测定指导的分级分离,从小花山柰提取物中分离出七种甲氧基黄酮衍生物(1-7),并根据光谱方法对它们进行了鉴定。在所测试的化合物中,5-羟基-3,7,3',4'-四甲氧基黄酮(5)对RBL-2H3细胞中抗原诱导的β-己糖胺酶释放具有最高的抗过敏活性,β-己糖胺酶释放作为脱颗粒的标志物,其IC(50)值为8.0 microM,其次是5-羟基-7-甲氧基黄酮(2,IC(50)=20.6 microM)和5-羟基-7,4'-二甲氧基黄酮(4,IC(50)=26.0 microM),而其他化合物表现出中等活性(IC(50)=37.5-66.5 microM)。7-甲氧基黄酮衍生物抗过敏活性的构效趋势可总结如下:(1)在3'和4'位用邻位甲氧基取代比仅进行一次甲氧基化具有更高的活性;(2)在3位进行甲氧基化会降低活性;(3)在5位进行甲氧基化比羟基化表现出更高的活性。还确定了化合物2、4和5对离子霉素诱导的β-己糖胺酶释放的作用机制。结果表明,化合物

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