School of Pharmaceutical Sciences, Binzhou Medical University, Yantai, PR China.
Sci Rep. 2017 Jun 14;7(1):3458. doi: 10.1038/s41598-017-02774-1.
Pulmonary rehabilitation mixture (PRM), a Chinese herbal medicine formula, has been used to treat pulmonary fibrosis for decades. In this study, we systematically evaluated the pharmacodynamic and pharmacokinetic performance of PRM. The pharmacodynamic results showed that PRM could improve the condition of CoCl-stimulated human type II alveolar epithelial cells, human pulmonary microvascular endothelial cells, human lung fibroblasts and pulmonary fibrosis rats induced by bleomycin, PRM treatment reduced the expression of platelet-derived growth factor, fibroblast growth factor, toll-like receptor 4, high-mobility group box protein 1 and hypoxia-inducible factor 1α. In the pharmacokinetic study, an accurate and sensitive ultra-high performance liquid chromatography tandem mass spectrometry method was developed and validated for the simultaneous determination of calycosin, calycosin-7-O-glucoside, formononetin, ononin and mangiferin of PRM in the rat plasma for the first time. The method was then successfully applied to the comparative pharmacokinetic study of PRM in normal and pulmonary fibrosis rats. The five constituents could be absorbed in the blood after the oral administration of PRM and exhibited different pharmacokinetic behaviors in normal and pulmonary fibrosis rats. In summary, PRM exhibited a satisfactory pharmacodynamic and pharmacokinetic performance, which highlights PRM as a potential multi-target oral drug for the treatment of pulmonary fibrosis.
肺康复合剂(PRM)是一种中药方剂,已用于治疗肺纤维化数十年。在这项研究中,我们系统地评估了 PRM 的药效学和药代动力学性能。药效学结果表明,PRM 可改善 CoCl 刺激的人 II 型肺泡上皮细胞、人肺微血管内皮细胞、人肺成纤维细胞和博莱霉素诱导的肺纤维化大鼠的状况,PRM 治疗可降低血小板衍生生长因子、成纤维细胞生长因子、Toll 样受体 4、高迁移率族蛋白 1 和缺氧诱导因子 1α 的表达。在药代动力学研究中,首次建立并验证了一种用于同时测定大鼠血浆中 PRM 中的毛蕊异黄酮、毛蕊异黄酮-7-O-葡萄糖苷、芒柄花素、大豆苷元和芒果苷的准确灵敏的超高效液相色谱-串联质谱法。该方法随后成功应用于 PRM 在正常和肺纤维化大鼠中的比较药代动力学研究。口服 PRM 后,这五种成分可以被血液吸收,并在正常和肺纤维化大鼠中表现出不同的药代动力学行为。总之,PRM 表现出令人满意的药效学和药代动力学性能,这突出了 PRM 作为一种潜在的多靶点口服药物,可用于治疗肺纤维化。