• Title of article

    TLR4-mediated anti-atherosclerosis mechanisms of angiotensin-converting enzyme inhibitor – Fosinopril

  • Author/Authors

    Yang، نويسنده , , Shuansuo and Li، نويسنده , , Ruogu and Tang، نويسنده , , Lei and Qu، نويسنده , , Xinkai and Ge، نويسنده , , Guanghao and Ma، نويسنده , , Jiangwei and Liu، نويسنده , , Huajin and Qiao، نويسنده , , Zengyong and Fang، نويسنده , , Weiyi، نويسنده ,

  • Issue Information
    روزنامه با شماره پیاپی سال 2013
  • Pages
    4
  • From page
    38
  • To page
    41
  • Abstract
    Recently, angiotensin-converting enzyme inhibitor (ACEI) has gained increasing attention for its anti-atherosclerosis activity, but the underlying mechanism is unknown. In our study, we used rabbits fed with high-fat forage, as an atherosclerosis model to investigate the effect of fosinopril, which is an ACEI. Animals which received both high-fat forage and fosinopril, were maintained as the drug-treated group. Ultrasonography and Sudan III staining were used to determine the process of atherosclerosis. The expression of TLR4 and activity NF-κB were determined using western blot, RT-PCR and ELISA. The results showed that the atherosclerotic plaque was visible at sixteen weeks. More importantly, the atherosclerotic plaque was significantly decreased after fosinopril treatment. In the atherosclerosis model, the levels of TLR4 and NF-κB were increased, but this increased expression was inhibited in the fosinopril treated group. Our results demonstrated that TLR4 could be used as a potential biomarker for atherosclerosis and ACEI has the potential to be a new anti-atherosclerotic drug.
  • Keywords
    NF-?B , fosinopril , TLR4 , atherosclerosis
  • Journal title
    Cellular Immunology
  • Serial Year
    2013
  • Journal title
    Cellular Immunology
  • Record number

    1848603