基于 MDCK-MDR1 细胞模型的 P-糖蛋白对 主要活性成分的血脑屏障转运的影响。
Effect of P-Glycoprotein on the Blood-Brain Barrier Transport of the Major Active Constituents of Based on the MDCK-MDR1 Cell Model.
机构信息
School of Pharmacy, Second Military Medical University, Shanghai200433, China.
Zhejiang Institute for Food and Drug Control, Hangzhou310057, China.
出版信息
ACS Chem Neurosci. 2023 Feb 15;14(4):766-772. doi: 10.1021/acschemneuro.2c00757. Epub 2023 Jan 27.
Bunge () is a traditional Chinese medicine that has been widely used in the treatment of various central nervous system (CNS) diseases. However, the mechanism of active components of crossing the blood-brain barrier (BBB) stays unclear. The purpose of this study was to clarify the mechanism of four ingredients of , i.e., cryptotanshinone (CTS), dihydrotanshinone I (DTS I), tanshinone IIA (TS IIA), and protocatechuic acid (PCTA) crossing the BBB using the in vitro model. The bidirectional transport of detectable components was tested using the MDCK-MDR1 monolayers. High performance liquid chromatography coupled to triple-quadrupole mass spectrometry (HPLC-QQQ/MS) was used to detect the content changes of monomer components transported through the BBB. of CTS, DTS I, and TS IIA in the absorption direction were lower than 1.0 × 10 cm/s, suggesting that these components were poorly absorbed, while PCTA was moderately absorbed through the BBB. The efflux ratio (ER) of CTS, DTS I, TS IIA, and PCTA were 1.65, 0.92, 4.27, and 1.48, respectively. After treatment with P-gp inhibitor tariquidar, the efflux ratio (ER) of CTS, DTS I, and TS IIA significantly decreased from 1.65 to 1.27, 0.92 to 0.36, and 4.27 to 0.86 ( < 0.05), respectively, while the efflux ratio of PCTA decreased without significance from 1.48 to 0.80. This indicated that the transport of CTS, DTS I, and TS IIA might be related to P-gp. TS IIA and CTS were verified as the substrates of P-gp among the four components since the ER of TS IIA and CTS is greater than 1.5. For PCTA and DTS I, their transport mechanism may be related to other transport proteins or passive transport. The results were confirmed by molecular docking in our current work. In this study, an in vitro BBB model was established and applied to the trans-BBB study of active components in for the first time, which may provide a basis for further research on the mechanisms of other TCMs in treating CNS diseases and is of great significance in promoting the rational and effective use of TCMs.
当归属(Bunge)是一种传统的中药,已被广泛应用于治疗各种中枢神经系统(CNS)疾病。然而,其活性成分穿越血脑屏障(BBB)的机制仍不清楚。本研究旨在阐明四种当归属成分,即隐丹参酮(CTS)、二氢丹参酮 I(DTS I)、丹参酮 IIA(TS IIA)和原儿茶酸(PCTA)穿越 BBB 的机制,使用体外模型。使用 MDCK-MDR1 单层来测试可检测成分的双向转运。高效液相色谱-三重四极杆质谱联用(HPLC-QQQ/MS)用于检测通过 BBB 转运的单体成分的含量变化。CTS、DTS I 和 TS IIA 在吸收方向的转运率(ER)均低于 1.0×10-6cm/s,表明这些成分吸收较差,而 PCTA 则适度地通过 BBB 吸收。CTS、DTS I、TS IIA 和 PCTA 的外排比(ER)分别为 1.65、0.92、4.27 和 1.48。用 P-糖蛋白抑制剂维拉帕米处理后,CTS、DTS I 和 TS IIA 的外排比(ER)分别从 1.65 显著降低至 1.27、0.92 降低至 0.36 和 4.27 降低至 0.86(<0.05),而 PCTA 的外排比没有显著降低,从 1.48 降低至 0.80。这表明 CTS、DTS I 和 TS IIA 的转运可能与 P-糖蛋白有关。在这四种成分中,TS IIA 和 CTS 被验证为 P-糖蛋白的底物,因为 TS IIA 和 CTS 的 ER 大于 1.5。对于 PCTA 和 DTS I,其转运机制可能与其他转运蛋白或被动转运有关。本研究通过分子对接对结果进行了验证。在本研究中,首次建立了体外 BBB 模型并应用于当归属活性成分的跨 BBB 研究,这可能为进一步研究其他中药治疗 CNS 疾病的机制提供依据,对促进中药的合理有效利用具有重要意义。