Wu Xiao-Li, Zheng Bin, Jin Li-Shuang, Zhang Ruo-Nan, He Ming, Yang Zhan, Wen Jin-Kun
Department of Biochemistry and Molecular Biology, Hebei Medical University Zhongshan East Road, Shijiazhuang 050017, China ; The Second Hospital of Hebei Medical University Shijiazhuang 050000, China.
Department of Biochemistry and Molecular Biology, Hebei Medical University Zhongshan East Road, Shijiazhuang 050017, China.
Int J Clin Exp Pathol. 2015 Jun 1;8(6):6323-33. eCollection 2015.
Oxidative stress and inflammation are the important pathological basis of atherogenesis. So, attenuating oxidative stress and inflammation has a very important significance in the prevention and treatment of atherosclerosis. The aim of present study was to investigate whether anti-atherosclerotic effect of Tongxinluo (TXL), a compound traditional Chinese medicine, is related to its anti-oxidation and anti-inflammation in human cardiac microvascular endothelial cells (HCMEC). We found that TXL treatment significantly reduced serum lipid levels and atherosclerotic plaque formation of apoE-deficient mice, and improved endothelial cell function as evidenced by increased expression of CD31 and eNOS. TXL pretreatment could abrogate the up-regulation of ROS and MDA induced by C16. Further experiments showed that the anti-oxidative effect of TXL may be related to inhibiting the expression of p22(phox), p47(phox) and HO-1 in HCMECs. We also found that TXL could inhibit the release of IL-1β and TNFα induced by C16, which is mediated by inhibiting the expression and activation of NF-κB. In conclusion, TXL decreases atherosclerotic plaque formation and improves endothelial cell function by inhibiting oxidative stress and inflammation in HCMECs. This finding provides a new molecular mechanism for the anti-atherosclerotic effect of TXL.
氧化应激和炎症是动脉粥样硬化发生的重要病理基础。因此,减轻氧化应激和炎症在动脉粥样硬化的防治中具有非常重要的意义。本研究的目的是探讨中药复方通心络(TXL)的抗动脉粥样硬化作用是否与其对人心脏微血管内皮细胞(HCMEC)的抗氧化和抗炎作用有关。我们发现,TXL治疗可显著降低载脂蛋白E缺陷小鼠的血脂水平和动脉粥样硬化斑块形成,并通过增加CD31和eNOS的表达证明其改善了内皮细胞功能。TXL预处理可消除C16诱导的ROS和MDA的上调。进一步的实验表明,TXL的抗氧化作用可能与抑制HCMECs中p22(phox)、p47(phox)和HO-1的表达有关。我们还发现,TXL可抑制C16诱导的IL-1β和TNFα的释放,这是通过抑制NF-κB的表达和激活介导的。总之,TXL通过抑制HCMECs中的氧化应激和炎症来减少动脉粥样硬化斑块形成并改善内皮细胞功能。这一发现为TXL的抗动脉粥样硬化作用提供了新的分子机制。