Department of Family Medicine, Tianjin United Family Hospital, Tianjin, China (mainland).
Tianjin Key Laboratory of Ionic-Molecular Function of Cardiovascular Disease, Department of Cardiology, Tianjin Institute of Cardiology, The Second Hospital of Tianjin Medical University, Tianjin, China (mainland).
Med Sci Monit. 2019 Dec 21;25:9811-9819. doi: 10.12659/MSM.917001.
BACKGROUND Ticagrelor is the first oral anti-platelet agent which has direct anti-platelet aggregation effect by combining with ADP P2Y12 receptors in platelets. It has been approved to reduce the incidence of thrombus cardiovascular events in acute coronary syndrome patients. However, the effects of ticagrelor on endothelial apoptosis have not been investigated. MATERIAL AND METHODS Oxidized low-density lipoprotein (ox-LDL) was used to establish a human umbilical vein endothelial cell (HUVEC) apoptosis model. To investigate the effects of ticagrelor on endothelial apoptosis, the HUVECs were treated with different dose of ticagrelor. Apoptosis rates of HUVECs was evaluated by flow cytometry, and the expression levels of Akt, p-Akt, Bcl-2, Bax, caspase-3, endothelial nitric oxide synthase (eNOS), and nitric oxide (NO) concentration were assessed. RESULTS After treatment with 50 ug/mL ox-LDL or 100 ug/mL ox-LDL, we found that the late apoptosis and necrosis rate and the expression levels of Bax and caspase-3 were significantly increased in HUVECs, whereas the expression levels of Akt, p-Akt, Bcl-2, eNOS, and NO were significantly decreased. Ticagrelor restored the apoptosis rate of ox-LDL-induced HUVECs in a dose-dependent manner. In addition, compared with ox-LDL group, ticagrelor treatment significantly increased the expression levels of Akt, p-Akt, Bcl-2, eNOS, and NO concentration, and significantly decreased the expression levels of Bax and caspase-3. CONCLUSIONS We found that ox-LDL induced significant apoptosis and necrosis in our model, which was dose-dependently improved by ticagrelor. These changes might be explained by alterations in apoptosis and antioxidant pathways.
替格瑞洛是首个通过与血小板 ADP P2Y12 受体结合而具有直接抗血小板聚集作用的口服抗血小板药物。它已被批准用于降低急性冠脉综合征患者血栓心血管事件的发生率。然而,替格瑞洛对血管内皮细胞凋亡的影响尚未得到研究。
使用氧化型低密度脂蛋白(ox-LDL)建立人脐静脉内皮细胞(HUVEC)凋亡模型。为了研究替格瑞洛对血管内皮细胞凋亡的影响,用不同剂量的替格瑞洛处理 HUVEC。用流式细胞术评估 HUVEC 的凋亡率,并检测 Akt、p-Akt、Bcl-2、Bax、caspase-3、内皮型一氧化氮合酶(eNOS)和一氧化氮(NO)浓度的表达水平。
用 50μg/ml ox-LDL 或 100μg/ml ox-LDL 处理后,我们发现 HUVEC 晚期凋亡和坏死率以及 Bax 和 caspase-3 的表达水平显著增加,而 Akt、p-Akt、Bcl-2、eNOS 和 NO 的表达水平显著降低。替格瑞洛以剂量依赖的方式恢复 ox-LDL 诱导的 HUVEC 凋亡率。此外,与 ox-LDL 组相比,替格瑞洛治疗显著增加了 Akt、p-Akt、Bcl-2、eNOS 和 NO 浓度的表达水平,同时显著降低了 Bax 和 caspase-3 的表达水平。
我们发现 ox-LDL 在我们的模型中诱导了显著的凋亡和坏死,而替格瑞洛则以剂量依赖的方式改善了这种情况。这些变化可能与凋亡和抗氧化途径的改变有关。