Xu Weizhe, Zhao Yan, Qin Yi, Ge Beikang, Gong Wenwen, Wu Yingting, Li Xiaorong, Zhao Yuming, Xu Pingxiang, Xue Ming
Department of Pharmacology, School of Basic Medical Sciences, Capital Medical University, Beijing 100069, China.
Core Facilities Center, Capital Medical University, Beijing 100069, China.
Molecules. 2016 Jul 1;21(7):874. doi: 10.3390/molecules21070874.
There is evidence suggesting that herbal extracts demonstrate greater bioactivities than their isolated constituents at an equivalent dose. This phenomenon could be attributed to the absence of interacting substances present in the extracts. By measuring the pharmacokinetic parameters of paeoniflorin (PF) and albiflorin (AF) after being orally administered to rats in isolated form, in combination with each other and within total peony glucosides (TPG), respectively, the current study aimed to identify positive pharmacokinetic interactions between components of peony radix extracts. Moreover, the pharmacokinetic profiles of PF and AF under normoxia and hypoxia were also investigated and compared. In order to achieve these goals, a highly sensitive and reproducible ultra-peformance liquid chromatography-mass spectrometry (UPLC-MS) method was developed and validated for simultaneously quantitation of PF and AF in rat plasma. This study found that compared with that of single component (PF/AF), the exposure of PF in rat plasma after combination administration or TPG administration was significantly increased, meanwhile the elimination of PF/AF was remarkably reduced. It was also noticed that AUC and Cmax of PF in hypoxia rats were significantly decreased compared with that of normaxia rats, suggesting that there was a decreased exposure of PF in rats under hypoxia. The current study, for the first time, revealed the pharmacokinetic interactions between PF/AF and other constitutes in TGP and the pharmacokinetic profiles of PF and AF under hypoxia. In view of the current findings, it could be supposed that the clinical performance of total peony glucosides would be better than that of single constitute (PF/AF). The outcomes of this animal study are expected to serve as a basis for development of clinical guidelines on total peony glucosides usage.
有证据表明,在等效剂量下,草药提取物比其分离出的成分具有更强的生物活性。这种现象可能归因于提取物中存在相互作用的物质。通过分别测量芍药苷(PF)和芍药内酯苷(AF)以分离形式、相互组合以及在总芍药苷(TPG)中口服给予大鼠后的药代动力学参数,本研究旨在确定芍药根提取物各成分之间的正向药代动力学相互作用。此外,还研究并比较了常氧和缺氧条件下PF和AF的药代动力学特征。为实现这些目标,开发并验证了一种高灵敏度且可重复的超高效液相色谱 - 质谱联用(UPLC - MS)方法,用于同时定量大鼠血浆中的PF和AF。本研究发现,与单一组分(PF/AF)相比,联合给药或TPG给药后大鼠血浆中PF的暴露量显著增加,同时PF/AF的消除明显减少。还注意到,缺氧大鼠中PF的AUC和Cmax与常氧大鼠相比显著降低,表明缺氧条件下大鼠体内PF的暴露量减少。本研究首次揭示了PF/AF与TGP中其他成分之间的药代动力学相互作用以及缺氧条件下PF和AF的药代动力学特征。鉴于目前的研究结果,可以推测总芍药苷的临床性能将优于单一成分(PF/AF)。这项动物研究的结果有望为制定总芍药苷使用的临床指南提供依据。