Zhao Tiechan, Chang Lianying, Zhang Boyong, Lu Ming, Wang Xiaoyi, Orgah John O, Wang Yuefei, Tian Xiaoxuan, Yang Jing, Fan Guanwei, Zhang Boli, Zhu Yan
Tianjin State Key Laboratory of Modern Chinese Medicine, Tianjin University of Traditional Chinese MedicineTianjin, China.
Research and Development Center of TCM, Tianjin International Joint Academy of Biotechnology and MedicineTianjin, China.
Front Pharmacol. 2017 Jun 13;8:361. doi: 10.3389/fphar.2017.00361. eCollection 2017.
Although single-targeting anti-platelet agents are used extensively in clinics, their limitations in resistance and bleeding have started a trend of combination therapy. Danhong injection (DHI) is a widely prescribed injection medicine for cardiovascular and cerebrovascular diseases in China. However, its precise clinical efficacy and functional components remain unexplored. In this study, we investigated the anti-thrombotic role and its chemical basis of DHI. In a photochemically-induced thrombosis model, DHI effectively dissolved thrombus and ameliorated its derived dry gangrene. DHI inhibited multiple GPCR agonists-induced platelet adhesion, aggregation and downstream Ca and cAMP signaling pathways. A functional screen of DHI library identified its major active components as a cluster of seven salvianolic acids. A combination of salvianolic acid A and C synergistically inhibited platelet aggregation while salvianolic acid B antagonized this effect. Our study revealed the anti-thrombotic activity of DHI. The multi-targeting mechanism of DHI proves the effectiveness of a natural anti-thrombotic combination therapy. The identification of salvianolic acids as a core anti-thrombotic activity of DHI and the discovery that their different combinations could either synergistically or antagonistically provide a better guidance for safer clinical application and paves the way for further development of DHI.
尽管单靶点抗血小板药物在临床上广泛应用,但其在耐药性和出血方面的局限性引发了联合治疗的趋势。丹红注射液(DHI)是中国广泛用于心脑血管疾病的注射药物。然而,其确切的临床疗效和功能成分仍未得到探索。在本研究中,我们研究了DHI的抗血栓作用及其化学基础。在光化学诱导的血栓形成模型中,DHI有效溶解血栓并改善其导致的干性坏疽。DHI抑制多种GPCR激动剂诱导的血小板黏附、聚集以及下游Ca和cAMP信号通路。对DHI文库进行功能筛选确定其主要活性成分是一组七种丹酚酸。丹酚酸A和C联合使用可协同抑制血小板聚集,而丹酚酸B则拮抗这种作用。我们的研究揭示了DHI的抗血栓活性。DHI的多靶点作用机制证明了天然抗血栓联合治疗的有效性。确定丹酚酸是DHI的核心抗血栓活性成分,以及发现它们不同的组合可能产生协同或拮抗作用,为更安全的临床应用提供了更好的指导,并为DHI的进一步开发铺平了道路。