State Key Laboratory of Drug Research, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai, 201203, China.
Translational Medicine Research Center, Medical Innovation Research Division and Fourth Medical Center of the Chinese PLA General Hospital, Beijing, 100853, China.
Acta Pharmacol Sin. 2024 May;45(5):1077-1092. doi: 10.1038/s41401-023-01224-1. Epub 2024 Jan 24.
Sepsis, a life-threatening health issue, lacks effective medicine targeting the septic response. In China, treatment combining the intravenous herbal medicine XueBiJing with conventional procedures reduces the 28-day mortality of critically ill patients by modulating septic response. In this study, we identified the combined active constituents that are responsible for the XueBiJing's anti-sepsis action. Sepsis was induced in rats by cecal ligation and puncture (CLP). The compounds were identified based on their systemic exposure levels and anti-sepsis activities in CLP rats that were given an intravenous bolus dose of XueBiJing. Furthermore, the identified compounds in combination were assessed, by comparing with XueBiJing, for levels of primary therapeutic outcome, pharmacokinetic equivalence, and pharmacokinetic compatibility. We showed that a total of 12 XueBiJing compounds, unchanged or metabolized, circulated with significant systemic exposure in CLP rats that received XueBiJing. Among these compounds, hydroxysafflor yellow A, paeoniflorin, oxypaeoniflorin, albiflorin, senkyunolide I, and tanshinol displayed significant anti-sepsis activities, which involved regulating immune responses, inhibiting excessive inflammation, modulating hemostasis, and improving organ function. A combination of the six compounds, with the same respective doses as in XueBiJing, displayed percentage survival and systemic exposure in CLP rats similar to those by XueBiJing. Both the combination and XueBiJing showed high degrees of pharmacokinetic compatibility regarding interactions among the six active compounds and influences of other circulating XueBiJing compounds. The identification of XueBiJing's pharmacologically significant constituents supports the medicine's anti-sepsis use and provides insights into a polypharmacology-based approach to develop medicines for effective sepsis management.
脓毒症是一种危及生命的健康问题,目前缺乏针对脓毒症反应的有效药物。在中国,将静脉用中药血必净与常规治疗相结合,可通过调节脓毒症反应降低危重症患者 28 天死亡率。本研究旨在确定血必净发挥抗脓毒症作用的联合活性成分。通过盲肠结扎穿孔(CLP)术诱导大鼠脓毒症。根据血必净在 CLP 大鼠中的系统暴露水平和抗脓毒症活性,确定化合物。此外,通过比较血必净,评估了鉴定出的组合化合物在主要治疗结果、药代动力学等效性和药代动力学兼容性方面的水平。我们表明,在接受血必净的 CLP 大鼠中,共有 12 种血必净化合物(未改变或代谢)以显著的全身暴露水平循环。在这些化合物中,羟基红花黄色素 A、芍药苷、氧化芍药苷、白芍苷、升麻素 I 和丹参醇显示出显著的抗脓毒症活性,涉及调节免疫反应、抑制过度炎症、调节止血和改善器官功能。六种化合物的组合,各自剂量与血必净相同,在 CLP 大鼠中的存活率和全身暴露率与血必净相似。组合和血必净在六种活性化合物之间的相互作用以及其他循环血必净化合物的影响方面均表现出高度的药代动力学兼容性。血必净中具有药理意义的成分的确定支持了该药的抗脓毒症用途,并为基于多药理学的方法开发有效管理脓毒症的药物提供了思路。