In vitro potential modulation of baicalin and baicalein on P-glycoprotein activity and expression in Caco-2 cells and rat gut sacs

被引:28
|
作者
Miao, Qing [1 ]
Wang, Zhiyong [1 ]
Zhang, Yuanyuan [1 ]
Miao, Peipei [1 ]
Zhao, Yuanyuan [1 ]
Zhang, Yujie [1 ]
Ma, Shuangcheng [2 ]
机构
[1] Beijing Univ Chinese Med, Sch Chinese Mat Med, 6 Zhonghuan South Rd, Beijing 100102, Peoples R China
[2] Natl Inst Food & Drug Control, 2 Tiantan Xili, Beijing 100050, Peoples R China
关键词
Inhibitors; P-glycoprotein (P-gp); Scutellariae Radix; structure-activity relationship; MULTIDRUG-RESISTANCE; MEDIATED-EFFLUX; REVERSAL; CANCER; INHIBITION; TRANSPORT; MODEL; PERMEABILITY; ENHANCEMENT; METABOLISM;
D O I
10.3109/13880209.2015.1107744
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Context Previous studies have shown that Scutellariae Radix, the dried root of Scutellaria baicalensis Georgi (Labiatae), has a certain inhibitory effect on P-glycoprotein (P-gp), but the effects of its main active constituents on P-gp are still ambiguous.ObjectivesIn vitro studies were performed to investigate the effects of its main active constituents (baicalin and its aglycone, baicalein) on the activity and expression of P-gp in intestine using Caco-2 cells and rat gut sacs.Materials and methods In Caco-2 cell experiments, the effects of baicalin and baicalein on P-gp activity were investigated using a P-gp substrate, rhodamine 123 and non-substrate fluorescein Na, by determining their intracellular fluorescence accumulation, and their effects on P-gp expression were determined using flow cytometry. In addition, rat gut sac model was selected to investigate the effects of baicalin and baicalein on the transport of verapamil, a classical P-gp substrate. The gut sacs of male Sprague-Dawley rats were filled with 0.4mL the test solution contained verapamil (0.2575mg/mL) and the drugs [baicalin and baicalein, at concentrations of 1/8 IC50 (59.875, 41.5g/mL), 1/4 IC50 (119.75, 83g/mL) and 1/2 IC50 (239.5, 166g/mL)], and then incubated in Tyrode's solution for a period of time. After termination of the incubation, the incubated solution was processed for the subsequent detection.Results According to the results of MTT assay, the IC50 values of verapamil, baicalin and baicalein were 104, 479, 332g/mL, respectively. The obtained results from the two models were confirmed mutually. As a result, baicalin exhibited no obvious effect on intracellular accumulation of Rh-123, and almost had no effect on P-gp expression and verapamil transportation, while baicalein significantly increased intracellular accumulation of Rh-123 (p<0.01), down-regulated P-gp expression (p<0.01) and increased the transport of verapamil (p<0.05).Discussion and conclusion The results indicated that baicalein may be a P-gp inhibitor, which presented obvious inhibitory effects on P-gp activity and expression level. A comparison of the structures of baicalin and baicalein indicates that the existence of glucosyl plays a decisive role in influencing the activity and expression of P-gp.
引用
收藏
页码:1548 / 1556
页数:9
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