Xu Jiazhen, Shen Yue, Luan Pengwei, Wang Haiying, Xu Yulan, Jiang Lixian, Li Ruixiang, Wang Feiyun, Zhu Yuying, Zhang Jiange
Research Center of Chiral Drugs, Innovation Research Institute of Traditional Chinese Medicine, Shanghai University of Traditional Chinese Medicine, Shanghai 201203, P.R. China.
Cancer Institute, The Affiliated Hospital of Qingdao University, Qingdao University, Qingdao Cancer Institute, Qingdao, Shandong 266071, P.R. China.
Exp Ther Med. 2023 Jul 10;26(2):409. doi: 10.3892/etm.2023.12108. eCollection 2023 Aug.
Salvianolate (Sal) is a medicinal composition that is widely used in China for the treatment of coronary heart disease and angina pectoris. The aim of the present study was to investigate the potential macrophage-mediated pro-angiogenic effects of Sal . In addition, another aim was to explore the effects of Sal in a rat model of transient middle cerebral artery occlusion (tMCAO) along with the potential mechanism by which it promotes angiogenesis. In this study, human umbilical vein endothelial cells (HUVECs) and Raw264.7 macrophages , and a rat tMCAO model were used to detect the pro-angiogenic effect and mechanism of Sal. The results of experiments showed that the viability, migration and tube formation of HUVECs were promoted by the supernatant of Sal-treated Raw264.7 macrophages (s-Sal) but not by Sal alone. s-Sal also increased the levels of phosphorylated (p-)VEGFR-2, p-AKT and p-p38 MAPK in HUVECs while Sal alone did not. , treatment with Sal significantly reduced the cerebral infarction volume and neurological deficit scores in the rat tMCAO model. Similar to the mechanism observed in the experiments, Sal treatment upregulated the protein expression of VEGF and VEGFR-2, in addition to the phosphorylation of VEGFR-2, AKT and p38, in the brain tissues of the tMCAO model rats. In summary, the results of the present study suggest that the mechanism of Sal-mediated angiogenesis is associated with stimulation of the VEGF/VEGFR-2 signaling pathway by macrophages. This suggests the potential of Sal as a therapeutic option for the treatment of acute cerebral ischemic injury, which may act via the promotion of angiogenesis.
丹参酚酸(Sal)是一种在中国广泛用于治疗冠心病和心绞痛的药物组合物。本研究的目的是探讨Sal潜在的巨噬细胞介导的促血管生成作用。此外,另一个目的是研究Sal在大鼠短暂性大脑中动脉闭塞(tMCAO)模型中的作用及其促进血管生成的潜在机制。在本研究中,使用人脐静脉内皮细胞(HUVECs)和Raw264.7巨噬细胞以及大鼠tMCAO模型来检测Sal的促血管生成作用及其机制。实验结果表明,Sal处理的Raw264.7巨噬细胞的上清液(s-Sal)可促进HUVECs的活力、迁移和管腔形成,而单独的Sal则无此作用。s-Sal还可增加HUVECs中磷酸化(p-)VEGFR-2、p-AKT和p-p38 MAPK的水平,而单独的Sal则不能。此外,Sal治疗可显著降低大鼠tMCAO模型中的脑梗死体积和神经功能缺损评分。与体外实验中观察到的机制相似,Sal治疗可上调tMCAO模型大鼠脑组织中VEGF和VEGFR-2的蛋白表达,以及VEGFR-2、AKT和p38的磷酸化水平。总之,本研究结果表明,Sal介导的血管生成机制与巨噬细胞对VEGF/VEGFR-2信号通路的刺激有关。这表明Sal作为治疗急性脑缺血损伤的治疗选择具有潜力,其可能通过促进血管生成发挥作用。