School of Chemistry and Chemical Engineering, Chongqing University, Chongqing 401331, China.
State Key Laboratory of Quality Research in Chinese Medicine, Institute of Chinese Medical Sciences, University of Macau, Macao SAR 999078, China.
Molecules. 2021 Dec 1;26(23):7293. doi: 10.3390/molecules26237293.
In this study; a spectrum-effect relationship analysis combined with a high-performance liquid chromatography-mass spectrometry (LC-MS) analysis was established to screen and identify active components that can inhibit thrombin and factor Xa (THR and FXa) in Salviae Miltiorrhizae Radix et Rhizoma-Chuanxiong Rhizoma (Danshen-Chuanxiong) herbal pair. Ten potential active compounds were predicted through a canonical correlation analysis (CCA), and eight of them were tentatively identified through an LC-MS analysis. Furthermore; the enzyme inhibitory activity of six available compounds; chlorogenic acid; -ligustilide; caffeic acid; ferulic acid; tanshinone I and tanshinone IIA; were tested to verify the feasibility of the method. Among them; chlorogenic acid was validated to possess a good THR inhibitory activity with IC of 185.08 µM. Tanshinone I and tanshinone IIA are potential FXa inhibitors with IC of 112.59 µM and 138.19 µM; respectively. Meanwhile; molecular docking results show that tanshinone I and tanshinone IIA; which both have binding energies of less than -7.0 kcal·mol; can interact with FXa by forming H-bonds with residues of SER214; GLY219 and GLN192. In short; the THR and FXa inhibitors in the Danshen-Chuanxiong herbal pair have been successfully characterized through a spectrum-effect relationship analysis and an LC-MS analysis.
在这项研究中,建立了一种基于光谱-效应关系分析结合高效液相色谱-质谱(LC-MS)分析的方法,用于筛选和鉴定能够抑制凝血酶和因子 Xa(THR 和 FXa)的丹参-川芎药对中的活性成分。通过典型相关分析(CCA)预测了 10 个潜在的活性化合物,通过 LC-MS 分析初步鉴定了其中的 8 个。此外,还测试了 6 种可用化合物——绿原酸、-藁本内酯、咖啡酸、阿魏酸、丹参酮 I 和丹参酮 IIA 的酶抑制活性,以验证该方法的可行性。其中,绿原酸被证实对 THR 具有良好的抑制活性,IC 为 185.08 µM。丹参酮 I 和丹参酮 IIA 是潜在的 FXa 抑制剂,IC 分别为 112.59 µM 和 138.19 µM。同时,分子对接结果表明,丹参酮 I 和丹参酮 IIA 均具有结合能小于-7.0 kcal·mol 的结合能,能够与 FXa 通过与残基 SER214、GLY219 和 GLN192 形成氢键相互作用。总之,通过光谱-效应关系分析和 LC-MS 分析,成功地对丹参-川芎药对中的 THR 和 FXa 抑制剂进行了表征。