Hu Yang-Xi, You Hong-Min, Ren Chang-Zhen, Hu Bo-Wen, Zhang Lu-Jun, Zhang Yan-Da, He Zhi-Qing, Ding Ru, Guo Zhi-Fu, Liang Chun
Department of Cardiology, Changzheng Hospital, Naval Medical University, Shanghai, 200003, China.
Department of Cardiology, Changhai Hospital, Naval Medical University, Shanghai, 200433, China.
BMC Complement Med Ther. 2022 Apr 22;22(1):112. doi: 10.1186/s12906-022-03589-y.
The compound Danshen Dripping Pill (CDDP), which is a mixture of extracts from Radix Salviae and Panax notoginseng, is a patented traditional Chinese medicine that is widely used in multiple countries for relieving coronary heart disease (CHD), but its pharmacological mechanism has not been fully elucidated. In this study, we screened the key pharmacological pathways and targets of CDDP that act on CHD using a network pharmacology-based strategy, and the angiogenic activity of CDDP was directly visually investigated in zebrafish embryos in vivo.
The potential therapeutic targets and pathways were predicted through a bioinformatics analysis. The proangiogenic effects of CDDP were examined using vascular sprouting assays on subintestinal vessels (SIVs) and optic arteries (OAs) as well as injury assays on intersegmental vessels (ISVs). Pharmacological experiments were applied to confirm the pathway involved.
Sixty-five potential therapeutic targets of CDDP on CHD were identified and enriched in the PI3K/AKT and VEGF/VEGFR pathways. An in vivo study revealed that CDDP promoted angiogenesis in SIVs and OAs in a dose-dependent manner and relieved the impairments in ISVs induced by lenvatinib, a VEGF receptor kinase inhibitor (VRI). In addition, Vegfaa and Kdrl expression were significantly upregulated after CDDP treatment. Furthermore, the proangiogenic effect of CDDP could be abolished by PI3K/AKT pathway inhibitors.
CDDP has a proangiogenic effect, the mechanism of which involves the VEGF/VEGFR and PI3K/AKT signaling pathways. These results suggest a new insight into the cardiovascular protective effect of CDDP.
复方丹参滴丸(CDDP)是丹参和三七提取物的混合物,是一种已获专利的传统中药,在多个国家广泛用于缓解冠心病(CHD),但其药理机制尚未完全阐明。在本研究中,我们使用基于网络药理学的策略筛选了CDDP作用于CHD的关键药理途径和靶点,并在斑马鱼胚胎体内直接直观地研究了CDDP的血管生成活性。
通过生物信息学分析预测潜在的治疗靶点和途径。使用对肠下血管(SIV)和视神经动脉(OA)的血管芽生试验以及对节间血管(ISV)的损伤试验来检测CDDP的促血管生成作用。应用药理学实验来确认所涉及的途径。
确定了CDDP对CHD的65个潜在治疗靶点,并在PI3K/AKT和VEGF/VEGFR途径中富集。体内研究表明,CDDP以剂量依赖性方式促进SIV和OA中的血管生成,并缓解由VEGF受体激酶抑制剂(VRI)乐伐替尼诱导的ISV损伤。此外,CDDP处理后Vegfaa和Kdrl表达显著上调。此外,PI3K/AKT途径抑制剂可消除CDDP的促血管生成作用。
CDDP具有促血管生成作用,其机制涉及VEGF/VEGFR和PI3K/AKT信号通路。这些结果为CDDP的心血管保护作用提供了新的见解。