Department of Pharmaceutics, College of Pharmacy, Shaanxi University of Chinese Medicine, Xianyang, 712046, Shaanxi, China.
Department of Pharmaceutics, College of Pharmacy, Shaanxi University of Chinese Medicine, Xianyang, 712046, Shaanxi, China; Key Laboratory of Basic and New Drug Research of Traditional Chinese Medicine, Shaanxi University of Chinese Medicine, Xianyang, 712046, Shaanxi, China.
Biomed Pharmacother. 2020 Oct;130:110563. doi: 10.1016/j.biopha.2020.110563. Epub 2020 Jul 31.
Carthamus tinctorius L.(Safflower), a herbal formula from Traditional Chinese Medicine (TCM), has been widely used for the treatment of cardio-cerebrovascular diseases, particularly cerebral infarction (CI) or cerebral ischemia-reperfusion injury. However, we know very little about the specific mechanisms associated with the therapeutic effect of Safflower on CI. In this study, we used a network pharmacology-based approach, together with rat model of CI, to gain more insight into of such mechanisms. Our analysis showed that Safflower contains 52 active compounds that target 247 genes, which were also cross-referenced with 299 genes associated with CI. Consequently, we identified 52 target genes in Safflower that were associated with CI. These 52 target genes were analyzed by gene ontology (GO) enrichment analysis, leading to the identification of 1491 biological process items, 90 molecular function items and 19 cell assembly items. Eighty-nine pathways were generated by KEGG enrichment (P < 0.05). Next, we investigated the effect of the extract of safflower (ES) and Safflower extract phospholipid complex (ESPC), delivered via the nasal route, on an animal model of the middle cerebral artery occlusion (MCAO). Our data confirmed that Safflower was able to treat CI by the regulating the TNF-α/MAPK pathway via CASP3. The therapeutic effect of ES and ESPC on CI acts by improving the circulation of blood in the central nervous system, reducing the inflammatory reaction, inhibiting apoptosis, and by protecting brain nerve cells from injury.
红花(Carthamus tinctorius L.),一种来自中医(TCM)的草药配方,已被广泛用于治疗心脑血管疾病,特别是脑梗死(CI)或脑缺血再灌注损伤。然而,我们对红花治疗 CI 的具体机制知之甚少。在这项研究中,我们使用了一种基于网络药理学的方法,结合大鼠 CI 模型,来更深入地了解这些机制。我们的分析表明,红花含有 52 种活性化合物,这些化合物可以靶向 247 个基因,这些基因也与 299 个与 CI 相关的基因交叉引用。因此,我们确定了红花中与 CI 相关的 52 个靶基因。对这些 52 个靶基因进行基因本体(GO)富集分析,鉴定出 1491 个生物过程项目、90 个分子功能项目和 19 个细胞组装项目。KEGG 富集分析生成了 89 条途径(P < 0.05)。接下来,我们研究了红花提取物(ES)和红花提取物磷脂复合物(ESPC)经鼻给药对大脑中动脉闭塞(MCAO)动物模型的影响。我们的数据证实,红花可以通过调节 TNF-α/MAPK 通路来治疗 CI,该通路通过 CASP3 发挥作用。ES 和 ESPC 对 CI 的治疗作用是通过改善中枢神经系统的血液循环、减少炎症反应、抑制细胞凋亡以及保护脑神经细胞免受损伤来实现的。