Pang Han-Qing, Xu Ding-Qiao, Tang Yu-Ping, Zhou Gui-Sheng, Xu Hui-Qin, Jin Yi, Zhu Zhen-Hua, Shi Xu-Qin, Yue Shi-Jun, Chen Yan-Yan, Huang Sheng-Liang, Duan Jin-Ao
Key Laboratory of Shaanxi Administration of Traditional Chinese Medicine for TCM C, and State Key Laboratory of Research & Development of Characteristic Qin Medicine Resources (Cultivation), and Shaanxi Key Laboratory of Chinese Medicine Fundamentals and New Drugs Research, and Shaanxi Collaborative Innovation Center of Chinese Medicinal Resources Industrialization, Shaanxi University of Chinese Medicine, Xi'an 712046, Shaanxi Province, China.
Jiangsu Collaborative Innovation Center of Chinese Medicinal Resources Industrialization, and National and Local Collaborative Engineering Center of Chinese Medicinal Resources Industrialization and Formulae Innovative Medicine, and Jiangsu Key Laboratory for High Technology Research of TCM Formulae, Nanjing University of Chinese Medicine, Nanjing 210023, Jiangsu Province, China.
Evid Based Complement Alternat Med. 2020 Sep 22;2020:9456350. doi: 10.1155/2020/9456350. eCollection 2020.
The present study aims to investigate the roles of herb pairs containing Angelicae Sinensis Radix (Danggui) in Xin-Sheng-Hua Granule (XSHG) on hemolytic and aplastic anemia (HAA) mice. HAA model mice were induced by acetyl phenylhydrazine and cyclophosphamide; then the samples of XSHG and its decomposed recipes (DY, DC, DT, DH, DJ, and DZ) were orally administrated to these mice. Indicators of peripheral blood routine, organ index, and ATPase activities were tested. Moreover, the main effective components in these samples were also analyzed by UHPLC-TQ-MS/MS. Clear separation between the control and model groups from score plot of principal component analysis (PCA) was easily seen, indicating that HAA model was successfully conducted. Afterwards, relative distance calculation method between dose groups and control group from PCA score plot was adopted to evaluate the integrated effects of hematinic function of different samples. And the orders of hematinic effects were as follows: XHSG > DJ > DT > DZ > DH > DC > DY. Further analysis of these samples by UHPLC-TQ-MS/MS revealed that XSHG underwent complicated changes when herb pairs containing Danggui were excluded from XSHG, respectively. Compared with XSHG, the vast majority of active compounds in sample DY (formula minus herb pair Danggui-Yimucao) decreased significantly, which could partly explain why herb pair Danggui-Yimucao made great contribution to XSHG. These findings showed that withdrawal analysis method is a valuable tool to analyze the impacts of herb pairs containing Danggui on XSHG, which could lay foundation to reveal the compatibility rules of this formula.
本研究旨在探讨新生化颗粒(XSHG)中含当归的药对在溶血性和再生障碍性贫血(HAA)小鼠中的作用。通过乙酰苯肼和环磷酰胺诱导建立HAA模型小鼠;然后将XSHG及其拆方(DY、DC、DT、DH、DJ和DZ)灌胃给予这些小鼠。检测外周血常规、器官指数和ATP酶活性指标。此外,还通过超高效液相色谱-串联四极杆质谱(UHPLC-TQ-MS/MS)分析了这些样品中的主要有效成分。从主成分分析(PCA)得分图中很容易看出对照组和模型组之间有明显分离,表明成功建立了HAA模型。之后,采用PCA得分图中剂量组与对照组之间的相对距离计算方法来评估不同样品补血功能的综合效果。补血作用顺序如下:XHSG>DJ>DT>DZ>DH>DC>DY。通过UHPLC-TQ-MS/MS对这些样品进行进一步分析发现,当XSHG分别排除含当归的药对时,其发生了复杂变化。与XSHG相比,样品DY(减去当归-益母草药对的方剂)中的绝大多数活性成分显著降低,这可以部分解释当归-益母草药对为何对XSHG有很大贡献。这些结果表明,拆方分析方法是分析含当归药对在XSHG中作用的一种有价值的工具,可为揭示该方剂的配伍规律奠定基础。