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
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