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迷迭香酸,[具体物质]的活性成分,通过调节Caco-2细胞中P-糖蛋白(P-gp)和乳腺癌耐药蛋白(BCRP)的表达及功能来改善格列喹酮的转运。

Rosmarinic acid, the active component of , improves gliquidone transport by regulating the expression and function of P-gp and BCRP in Caco-2 cells.

作者信息

Li Mengying, Yin Dengke, Li Jiachen, Shao Fuping, Zhang Qingqing, Jiang Qianqian, Zhang Mengmeng, Yang Ye

出版信息

Pharmazie. 2020 Jan 2;75(1):18-22. doi: 10.1691/ph.2020.9754.

DOI:10.1691/ph.2020.9754
PMID:32033628
Abstract

(Danshen) is typically used in the treatment of diabetic complications and is often co-prescribed with gliquidone in China. However, whether danshen affects the absorption of gliquidone has not been elucidated. In this study, the effects of an aqueous extract of danshen (danshen injection, DSI) and its primary compounds (danshensu, protocatechuic aldehyde, rosmarinic acid and salvianolic acid B) on gliquidone transport across Caco-2 monolayer cells was investigated. DSI enhanced the transport of gliquidone in Caco-2 cell monolayers from the apical (AP) to basolateral (BL) sides and from the BL to AP sides. Rosmarinic acid (RA) also significantly increased the Papp (AP-BL) value for gliquidone transport. Verapamil (a P-gp inhibitor) and Ko143 (a BCRP inhibitor) inhibited the BL-AP transport of gliquidone and promoted the AP-BL transport of gliquidone, whereas MK571 (an MRP1 inhibitor), probenecid (an MRP2 inhibitor), and benzbromarone (an MRP3 inhibitor) had no effect on gliquidone transport. RA also enhanced the intracellular accumulation of Rho123 and Hoechst 33342. The expression of P-gp and BCRP was significantly downregulated, and P-gp ATPase activity was promoted by RA in a dose-dependent manner. These results indicate that an aqueous extract of danshen can increase the transport of gliquidone in Caco-2 cell monolayers and that RA may be the primary compound associated with this activity, which is in agreement with RA simultaneously suppressing the function and expression of P-gp and BCRP.

摘要

丹参通常用于治疗糖尿病并发症,在中国常与格列喹酮联合使用。然而,丹参是否会影响格列喹酮的吸收尚未阐明。在本研究中,考察了丹参水提取物(丹参注射液,DSI)及其主要成分(丹参素、原儿茶醛、迷迭香酸和丹酚酸B)对格列喹酮跨Caco-2单层细胞转运的影响。DSI增强了格列喹酮在Caco-2细胞单层中从顶端(AP)到基底外侧(BL)以及从BL到AP方向的转运。迷迭香酸(RA)也显著增加了格列喹酮转运的表观渗透系数(Papp,AP-BL)值。维拉帕米(一种P-糖蛋白抑制剂)和Ko143(一种乳腺癌耐药蛋白抑制剂)抑制了格列喹酮的BL-AP转运并促进了AP-BL转运,而MK571(一种多药耐药相关蛋白1抑制剂)、丙磺舒(一种多药耐药相关蛋白2抑制剂)和苯溴马隆(一种多药耐药相关蛋白3抑制剂)对格列喹酮转运没有影响。RA还增强了罗丹明123和Hoechst 33342的细胞内蓄积。RA以剂量依赖性方式显著下调P-糖蛋白和乳腺癌耐药蛋白的表达,并促进P-糖蛋白ATP酶活性。这些结果表明,丹参水提取物可增加格列喹酮在Caco-2细胞单层中的转运,RA可能是与此活性相关的主要成分,这与RA同时抑制P-糖蛋白和乳腺癌耐药蛋白的功能及表达一致。

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