School of Traditional Chinese Materia Medica, Shenyang Pharmaceutical University, Shenyang 110016, China.
School of Pharmacy, Shenyang Pharmaceutical University, Shenyang 110016, China.
Phytomedicine. 2018 Sep 15;48:141-151. doi: 10.1016/j.phymed.2018.04.041. Epub 2018 Apr 17.
Primary dysmenorrhea (PDM) is one of the most common gynaecological disorders among women, which seriously affects women's life quality due to its high incidence rate. Guizhi Fuling capsule (GZFLC), a well-known traditional Chinese medical prescription, has been widely used to treat gynecological blood stasis syndromes such as PDM. However, its mechanisms of action and combination were still unknown.
The aim of this study was to develop a pharmacokinetic-pharmacodynamic (PK-PD) model to assess time-concentration-effect relationships for anti-dysmenorrhea effect of GZFLC and provide better understanding for mechanisms of action and combination of GZFLC.
The PDM rats model was induced by oxytocin exposure following estradiol benzoate pretreatment. Gallic acid (GA), amygdalin (AMY), albiflorin (ALB), prunasin (PA) and cinnamic acid (CA) were evaluated as bioactive ingredients for investigating PK processes. GA, AMY, ALB and PA exhibited appropriate PK parameters and were selected as the PK markers to map the anti-dysmenorrhea effect of GZFLC. A PK-PD model was established on the basis of GA, AMY, ALB and PA plasma concentrations vs. the values of two ratios (PGE/PGF and 6-Keto-PGF/TXB), by a two-compartment PK model with a simple E model to explain the time delay between the drug plasma concentrations of PK markers and the anti-dysmenorrhea effect.
The PDM rat model has been successfully established. Compared with the normal treated group, the bioactive ingredients in PDM treated group exhibited significant changing trends of PK behaviors, such as better absorption and distribution, slower elimination and delays in reaching the maximum concentration (T). The analysis of PK-PD parameters indicated that the active metabolites and prototypes of bioactive ingredients in GZFLC were inclined to regulate the activity of prostacyclin synthetase and thromboxane synthetase to control the production of TXA and PGI so as to treat PDM. As the main effective medicinal materials for the treatment of PDM in GZFLC prescription Persicae Semen, Moutan Cortex and Paeonia lactiflora Pall, Persicae Semen played the most important role, while the role of Paeonia lactiflora Pall was the weakest.
The PK-PD model results provided scientific basis for clarifying compatibility mechanisms of GZFLC prescription and a better understanding for biosynthetic mechanisms of four prostaglandins (PGE, PGF, 6-Keto-PGF and TXB) in the treatment of PDM by GZFLC. Investigations on the relationship between the effects and the bioactive ingredients are of benefit to explore the mechanisms of action and combination for traditional Chinese medical prescriptions (TCP) and facilitate the development of future clinical applications of TCP.
原发性痛经(PDM)是女性中最常见的妇科疾病之一,由于其高发病率,严重影响了女性的生活质量。桂枝茯苓胶囊(GZFLC)是一种著名的中药方剂,已广泛用于治疗 PDM 等妇科血瘀证。然而,其作用机制和组合仍不清楚。
本研究旨在建立药代动力学-药效学(PK-PD)模型,以评估 GZFLC 抗痛经作用的时浓度-效应关系,并为 GZFLC 的作用机制和组合提供更好的理解。
采用雌二醇苯甲酸预处理后催产素诱导 PDM 大鼠模型。评估没食子酸(GA)、苦杏仁苷(AMY)、白芍苷(ALB)、苯丁腈苷(PA)和肉桂酸(CA)作为生物活性成分,研究 PK 过程。GA、AMY、ALB 和 PA 表现出适当的 PK 参数,被选为 PK 标志物,以映射 GZFLC 的抗痛经作用。基于 GA、AMY、ALB 和 PA 血浆浓度与两个比值(PGE/PGF 和 6-Keto-PGF/TXB),通过两室 PK 模型和简单 E 模型建立 PK-PD 模型,解释 PK 标志物的药物血浆浓度与抗痛经作用之间的时间延迟。
成功建立了 PDM 大鼠模型。与正常治疗组相比,PDM 治疗组的生物活性成分 PK 行为表现出明显的变化趋势,如更好的吸收和分布、更慢的消除和达到最大浓度(T)的延迟。PK-PD 参数分析表明,GZFLC 中生物活性成分的活性代谢物和原型倾向于调节前列环素合成酶和血栓素合成酶的活性,以控制 TXA 和 PGI 的产生,从而治疗 PDM。作为 GZFLC 处方中治疗 PDM 的主要有效药材,桃仁、牡丹皮和白芍,桃仁的作用最重要,而白芍的作用最弱。
PK-PD 模型结果为阐明 GZFLC 处方的配伍机制提供了科学依据,为 GZFLC 治疗 PDM 时四种前列腺素(PGE、PGF、6-Keto-PGF 和 TXB)的生物合成机制提供了更好的理解。研究作用与生物活性成分之间的关系有助于探索中药方剂(TCP)的作用机制和组合,促进 TCP 未来的临床应用。