Ma Xiangwei, Chen Yanyu, Jiang Shumin, Zhao Xiaoping
College of Pharmaceutical Sciences, Zhejiang Chinese Medical University, Hangzhou, China.
School of Basic Medical Sciences, Zhejiang Chinese Medical University, Hangzhou, China.
Front Pharmacol. 2021 Mar 8;12:623533. doi: 10.3389/fphar.2021.623533. eCollection 2021.
Quality control of Chinese medicine (CM) is mainly based on chemical testing, which sometimes shows weak correlation to pharmacological effects. Thus, there is a great demand to establish bioactivity-based assays to ensure the quality of CM. The aim of the present study was to establish a bioassay-based approach to evaluate the biological activity of Xuesaitong injection (XST) based on an zebrafish model. Zebrafish larvae with arachidonic acid (AA)-induced thrombus were applied to evaluate anti-thrombosis effects of XST and explore the potential mechanism of XST. Analysis of major components in normal and abnormal XST samples was performed by high performance liquid chromatography (HPLC). The results indicate that XST could significantly restore heart red blood cells (RBCs) intensity of thrombotic zebrafish in a dose-dependent manner, whilst decreasing RBCs accumulation in the caudal vein. The results were confirmed using a green fluorescence protein (GFP)-labeled zebrafish thrombosis model. Moreover, we could show that XST downregulates the expression of the () gene to inhibit the coagulation cascade during the process of thrombosis in zebrafish. Notoginsenoside R ginsenoside Rg, ginsenoside Rb and ginsenoside Rd, which were considered to be the major components of XST, also showed moderate anti-thrombosis efficacy. Further results showed that the zebrafish thrombosis model could efficiently distinguish five abnormal batches of XST from 24 normal batches. Furthermore, the inhibition rates of different batches were correlated with the content level of major components. Our results suggested that the proposed zebrafish thrombosis model could be successfully used to evaluate the batch-to-batch consistency of XST, which provided an alternative way for the quality control of CM.
中药质量控制主要基于化学检测,而化学检测有时与药理作用的相关性较弱。因此,迫切需要建立基于生物活性的检测方法来确保中药质量。本研究的目的是基于斑马鱼模型建立一种基于生物测定的方法来评估血塞通注射液(XST)的生物活性。应用花生四烯酸(AA)诱导血栓形成的斑马鱼幼虫来评估XST的抗血栓作用,并探索XST的潜在作用机制。通过高效液相色谱(HPLC)对正常和异常XST样品中的主要成分进行分析。结果表明,XST能以剂量依赖性方式显著恢复血栓形成斑马鱼的心脏红细胞(RBC)强度,同时减少尾静脉中RBC的聚集。使用绿色荧光蛋白(GFP)标记的斑马鱼血栓形成模型证实了该结果。此外,我们发现XST在斑马鱼血栓形成过程中下调()基因的表达以抑制凝血级联反应。被认为是XST主要成分的三七皂苷R、人参皂苷Rg、人参皂苷Rb和人参皂苷Rd也显示出适度的抗血栓功效。进一步的结果表明,斑马鱼血栓形成模型能够有效区分24个正常批次中的5个异常批次的XST。此外,不同批次的抑制率与主要成分的含量水平相关。我们的结果表明,所提出的斑马鱼血栓形成模型可成功用于评估XST的批次间一致性,为中药质量控制提供了一种替代方法。