...
首页> 外文期刊>Molecules >Absorption and Interaction of the Main Constituents from the Traditional Chinese Drug Pair Shaoyao-Gancao via a Caco-2 Cell Monolayer Model
【24h】

Absorption and Interaction of the Main Constituents from the Traditional Chinese Drug Pair Shaoyao-Gancao via a Caco-2 Cell Monolayer Model

机译:中药对Sha药-甘草的主要成分通过Caco-2细胞单层模型的吸收与相互作用

获取原文

摘要

Shaoyao-Gancao (Paeoniae Radix Alba and Glycyrrhizae Radix et Rhizoma) is a traditional Chinese drug pair widely used in decoctions for relieving pains, especially abdominal pain. We aimed to determine the intestinal absorption and interaction of three active compounds (glycyrrhizic acid, liquiritin, and paeoniflorin) in this drug pair. We investigated the transport of these compounds across intestinal epithelial cells by using the Caco-2 cell monolayer in both the apical-to-basolateral (A-B) and B-A directions. All compounds could only travel through the Caco-2 cell monolayer at a low level when the cells were treated with single component solutions. In the presence of verapamil, an inhibitor of P-glycoprotein (P-gp), the absorptive permeability (PAB) of paeoniflorin and liquiritin increased significantly (p 0.05) and efflux ratios decreased, while the absorption of glycyrrhizic acid did not change significantly, which indicated that paeoniflorin and liquiritin might be P-gp substrates. In addition, when liquiritin and glycyrrhizic acid in Gancao extract and paeoniflorin in Shaoyao extract were examined, PAB of paeoniflorin and liquiritin were significantly higher, while glycyrrhizic acid retained the same absorption level compared to the corresponding single component solutions, which suggested that some certain ingredients in the extracts can promote the absorption of paeoniflorin and liquiritin, but not that of glycyrrhizic acid. Furthermore, compared to the results of treatment with individual extracts, treatment of cells with a mixture of the two extracts considerably increased (p 0.05) the absorption of glycyrrhizic acid and paeoniflorin and showed no change in the absorption of liquiritin, which implied that the transport of glycyrrhizic acid and paeoniflorin is increased by some ingredients from the complementary drug in the drug pair, while that of liquiritin remains unaffected.
机译:oy药-甘草(Pa药甘草和甘草)是一种传统中药,广泛用于减轻疼痛,特别是腹痛的汤剂中。我们的目的是确定该药对中三种活性化合物(甘草酸,液体白蛋白和pa药苷)的肠道吸收和相互作用。我们研究了通过使用Caco-2细胞单层在顶端到基底外侧(A-B)和B-A方向跨肠道上皮细胞运输这些化合物。当用单组分溶液处理细胞时,所有化合物只能以低水平通过Caco-2细胞单层。在维拉帕米存在下,P-糖蛋白(P-gp)抑制剂会使pa药苷和脂蛋白的吸收通透性(P AB )显着增加(p <0.05),流出比降低,而甘草酸的吸收没有显着变化,这表明pa药苷和脂蛋白可能是P-gp的底物。此外,当检查甘草提取物中的甘草酸和甘草酸以及少药提取物中的pa药苷时,pa药苷和草甘肽的P AB 显着较高,而甘草酸与相应的单一组分相比保持相同的吸收水平。解决方案,这表明提取物中的某些特定成分可以促进pa药苷和脂蛋白的吸收,但不能促进甘草酸的吸收。此外,与用单个提取物处理的结果相比,用两种提取物的混合物处理细胞可显着提高(p <0.05)甘草酸和pa药苷的吸收,并且显示脂蛋白的吸收没有变化,这表明药物对中补充药物中的某些成分增加了甘草酸和pa药苷的转运,而脂蛋白的转运却不受影响。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号