Ma Jing, Ren Yue, Zhao Bo-Wen, Lin Li, Zhang Yan-Ling
Engineering Research Center of Key Technologies for Traditional Chinese Medicine Pharmacy and New Drug Development of Ministry of Education, Research Center of Traditional Chinese Medicine-Information Engineering of National Administration of Traditional Chinese Medicine, School of Chinese Materia Medica, Beijing University of Chinese Medicine Beijing 102488,China.
Beijing Key Laboratory of Pharmacology of Chinese Materia Medica, Institute of Basic Medical Sciences of Xiyuan Hospital, China Academy of Chinese Medical Sciences Beijing 100091, China.
Zhongguo Zhong Yao Za Zhi. 2021 Dec;46(23):6243-6250. doi: 10.19540/j.cnki.cjcmm.20210830.401.
As a classic prescription for promoting blood circulation to remove blood stasis, Xuefu Zhuyu Decoction(XFZYD) is widely used in clinical practice and has notable curative effect. Based on the key targets of activating blood circulation, this study identified the active components of XFZYD to reveal the material basis. The components of XFZYD were collected from Traditional Chinese Medicine Systems Pharmacology Database and Analysis Platform(TCMSP). The molecular docking models were built for the blood-activating targets obtained from the previous study with the components of XFZYD. The top five active components with measurability for each target were selected as the potential blood-activating components in the prescription. The efficacy of the prescription can embody key pharmacological and high-content components. In this study, anti-platelet aggregation activity was used to characterize the effect of activating blood, and the in vivo experiments were conducted to verify the accuracy of the active components. A total of 210 chemical components of XFZYD were screened out from TCMSP and docked with the key targets with the function of activating blood. Ligustrazine, acteoside, naringin, etc. were selected as the potential active components for activating blood in XFZYD. The anti-platelet aggregation activity of the combination of Chuanxiong Rhizoma, Rehmanniae Radix, Aurantii Fructus, Glycyrrhizae Radix et Rhizoma, and Carthami Flos was 9.82%±5.11%. Compared with that in the control group, the platelet aggregation induced by adenosine diphosphate(ADP) was significantly inhibited in the test group(P<0.01), which verified the accuracy of the active components. This study can guide the research on the material basis of XFZYD and provide insights into the development and utilization of the classical prescription.
血府逐瘀汤作为活血化瘀的经典方剂,在临床实践中广泛应用且疗效显著。本研究基于活血化瘀的关键靶点,鉴定血府逐瘀汤的活性成分以揭示其物质基础。血府逐瘀汤的成分从中药系统药理学数据库与分析平台(TCMSP)收集。针对前期研究获得的活血靶点与血府逐瘀汤的成分构建分子对接模型。为该方剂中每个靶点选择可测量的前五位活性成分作为潜在的活血成分。方剂的疗效可体现关键药理成分和高含量成分。本研究采用抗血小板聚集活性表征活血作用,并通过体内实验验证活性成分的准确性。从TCMSP筛选出血府逐瘀汤共210种化学成分,并与具有活血功能的关键靶点进行对接。川芎嗪、毛蕊花糖苷、柚皮苷等被选为血府逐瘀汤中潜在的活血活性成分。川芎、生地黄、枳壳、甘草和红花组合的抗血小板聚集活性为9.82%±5.11%。与对照组相比,试验组二磷酸腺苷(ADP)诱导的血小板聚集受到显著抑制(P<0.01),验证了活性成分的准确性。本研究可为血府逐瘀汤物质基础的研究提供指导,并为经典方剂的开发利用提供思路。