Jiang Hua, Qu Peng
Department of Cardiology, The Second Affiliated Hospital of Dalian Medical University, Dalian, Liaoning 116027, P.R. China.
Exp Ther Med. 2017 Dec;14(6):5857-5862. doi: 10.3892/etm.2017.5313. Epub 2017 Oct 16.
The present study investigated the effects of leaf extract (GBE50) on lipopolysaccharide (LPS) induced Toll-like receptor 4 (TLR4)/nuclear factor-κB (NF-κB) signaling pathway and its effects on angiotensinogen (ATG) and AT receptor, so as to explore the mechanism of GBE50 in prevention and treatment of left ventricular remodeling. cultured neonatal rat ventricular myocytes (NRVMs) were divided into 4 groups including i) control group: DMEM medium; ii) LPS group: iii) LPS + GBE50 group; iv) LPS + caffeic acid phenethyl ester (CAPE, specific inhibitor of NF-κB) group. Nuclear translocation of NF-κB p65 was detected by immunocytochemical method after intervention for 24 h. Expression of TLR4, ATG, AT receptors and β-myosin heavy chain (β-MHC) mRNA were detected by reverse transcription-polymerase chain reaction (RT-PCR). Protein content of cardiomyocytes was measured by Coomassie Brilliant Blue method. Under LPS stimulation, expression level of TLR4 mRNA in NRVMs was significantly increased (P<0.01), nuclear translocation of NF-κB p65 was increased, expression levels of ATG, AT receptor and β-MHC mRNA and the protein content in cells were also increased significantly (P<0.01). GBE50 and CAPE significantly inhibited nuclear translocation of NF-κB p65. GBE50 and CAPE treatments also reduced the increased mRNA levels of TLR4, ATG, AT receptor and β-MHC and protein content in cell caused by LPS stimulation. We concluded that, GBE50 can inhibit the activation of local renin-angiotensin system by inhibiting the activation of TLR4/NF-κB and TLR4/NF-κB, signaling pathway inhibition may be one of the mechanisms of the role of leaf extract in preventing myocardial remodeling.
本研究探讨叶提取物(GBE50)对脂多糖(LPS)诱导的Toll样受体4(TLR4)/核因子κB(NF-κB)信号通路的影响及其对血管紧张素原(ATG)和AT受体的作用,以探讨GBE50防治左心室重构的机制。将培养的新生大鼠心室肌细胞(NRVMs)分为4组,包括:i)对照组:DMEM培养基;ii)LPS组;iii)LPS + GBE50组;iv)LPS + 咖啡酸苯乙酯(CAPE,NF-κB特异性抑制剂)组。干预24小时后,采用免疫细胞化学方法检测NF-κB p65的核转位。采用逆转录-聚合酶链反应(RT-PCR)检测TLR4、ATG、AT受体和β-肌球蛋白重链(β-MHC)mRNA的表达。采用考马斯亮蓝法测定心肌细胞蛋白含量。在LPS刺激下,NRVMs中TLR4 mRNA表达水平显著升高(P<0.01),NF-κB p65核转位增加,ATG、AT受体和β-MHC mRNA表达水平及细胞内蛋白含量也显著增加(P<0.01)。GBE50和CAPE显著抑制NF-κB p65的核转位。GBE50和CAPE处理还降低了LPS刺激引起的TLR4、ATG、AT受体和β-MHC mRNA水平升高及细胞内蛋白含量。我们得出结论,GBE50可通过抑制TLR4/NF-κB的激活来抑制局部肾素-血管紧张素系统的激活,TLR4/NF-κB信号通路抑制可能是叶提取物预防心肌重构作用的机制之一。