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假马齿苋标准化提取物及其五种单一活性成分对人P-糖蛋白活性的体外作用。

In vitro effects of standardized extract of Bacopa monniera and its five individual active constituents on human P-glycoprotein activity.

作者信息

Singh Rajbir, Rachumallu Ramakrishna, Bhateria Manisha, Panduri Jagadeesh, Bhatta Rabi Sankar

机构信息

Pharmacokinetics and Metabolism Division, CSIR - Central Drug Research Institute , Lucknow, Uttar Pradesh , India .

出版信息

Xenobiotica. 2015;45(8):741-9. doi: 10.3109/00498254.2015.1017752. Epub 2015 Apr 14.

DOI:10.3109/00498254.2015.1017752
PMID:25869246
Abstract

1. For centuries Bacopa monniera (BM) has been used as an herbal drug for the treatment of various mental ailments. A chemically standardized alcoholic extract of BM is clinically available over the counter herbal remedy for memory enhancement in children and adults. Consumption of herbal preparations has been reported to alter the function of membrane transporters, especially P-glycoprotein (P-gp), ATP-dependent drug efflux transporter responsible for the development of herb-drug interactions. 2. In the present study, we evaluated the in vitro effect of BM extract and its five individual active constituents (namely, bacopaside I, bacopaside II and bacopasaponin C, bacoside A and bacoside A3) on P-gp function using luminescent P-gp ATPase assay and Rh123 transport assay across human MDR1 gene transfected LLC-GA5-COL150 cell line. 3. It was observed that BM extract and its five individual constituents inhibited both basal activity as well as verapamil-stimulated ATPase activity, suggesting their affinity towards P-gp. Further, BM and its five active constituents inhibited the rhodamine 123 (Rh123) transport across LLC-GA5-COL150 cell monolayer with bacopaside II being the most potent inhibitor of P-gp, which decreased P-gp efflux ratio of Rh123 by fourfold in comparison to control. 4. Our finding may prove beneficial in predicting the potential herb-drug interactions of BM on concomitant medication with P-gp substrate drugs in clinical settings.

摘要
  1. 几个世纪以来,假马齿苋一直被用作治疗各种精神疾病的草药。一种经过化学标准化的假马齿苋酒精提取物在临床上是一种非处方草药疗法,用于增强儿童和成人的记忆力。据报道,食用草药制剂会改变膜转运蛋白的功能,尤其是P-糖蛋白(P-gp),这是一种依赖ATP的药物外排转运蛋白,与草药-药物相互作用的发生有关。2. 在本研究中,我们使用发光P-gp ATP酶测定法和Rh123转运测定法,评估了假马齿苋提取物及其五种单独的活性成分(即假马齿苋苷I、假马齿苋苷II、假马齿苋皂苷C、假马齿苋皂苷A和假马齿苋皂苷A3)对人MDR1基因转染的LLC-GA5-COL150细胞系中P-gp功能的体外影响。3. 观察到假马齿苋提取物及其五种单独成分均抑制基础活性以及维拉帕米刺激的ATP酶活性,表明它们对P-gp具有亲和力。此外,假马齿苋及其五种活性成分抑制了罗丹明123(Rh123)跨LLC-GA5-COL150细胞单层的转运,其中假马齿苋苷II是最有效的P-gp抑制剂,与对照组相比,它使Rh123的P-gp外排率降低了四倍。4. 我们的发现可能有助于预测在临床环境中假马齿苋与P-gp底物药物同时使用时潜在的草药-药物相互作用。

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