Yuan Huajing, Liu Yang, Huang Kai, Hao Hao, Xue Yi-Tao
Shandong University of Traditional Chinese Medicine, Jinan 250014, China.
Affiliated Hospital of Shandong University of Traditional Chinese Medicine, Jinan 250014, China.
Evid Based Complement Alternat Med. 2022 Aug 26;2022:9686149. doi: 10.1155/2022/9686149. eCollection 2022.
At present, although the early treatment of sepsis is advocated, the treatment effect of sepsis is unsatisfactory, and the mortality rate remains high. Shenfu injection (SFI) has been used to treat sepsis with good clinical efficacy. Based on network pharmacology, this study adopted a new research strategy to identify the potential therapeutic targets and key active ingredients of SFI for sepsis from the perspective of the pathophysiology of sepsis. This analysis identified 28 active ingredients of SFI based on UHPLC-QQQ MS, including 18 ginsenosides and 10 aconite alkaloids. 59 targets were associated with the glycocalyx and sepsis pathways. Based on the number of targets related to the pathophysiological process of sepsis, we identified songorine, ginsenoside Rf, ginsenoside Re, and karacoline as the key active ingredients of SFI for the treatment of sepsis. According to the cluster analysis of MCODE and the validation on the GEO dataset, LGALS3, BCHE, AKT1, and IL2 were identified as the core targets. This study further explored the therapeutic mechanism and the key active ingredients of SFI in sepsis and provided candidate compounds for drug development.
目前,尽管提倡对脓毒症进行早期治疗,但脓毒症的治疗效果仍不尽人意,死亡率居高不下。参附注射液(SFI)已被用于治疗脓毒症,临床疗效良好。基于网络药理学,本研究采用了一种新的研究策略,从脓毒症的病理生理学角度确定SFI治疗脓毒症的潜在治疗靶点和关键活性成分。该分析基于超高效液相色谱-串联四极杆质谱(UHPLC-QQQ MS)鉴定出SFI的28种活性成分,包括18种人参皂苷和10种附子生物碱。59个靶点与糖萼和脓毒症通路相关。基于与脓毒症病理生理过程相关的靶点数量,我们确定了松贝碱、人参皂苷Rf、人参皂苷Re和卡拉可林为SFI治疗脓毒症的关键活性成分。根据MCODE聚类分析和在GEO数据集上的验证,确定LGALS3、BCHE、AKT1和IL2为核心靶点。本研究进一步探索了SFI治疗脓毒症的作用机制和关键活性成分,为药物研发提供了候选化合物。