Department of Surgery, Thomas Jefferson University, Philadelphia, Pennsylvania 19017, USA.
J Surg Res. 2010 Oct;163(2):e113-22. doi: 10.1016/j.jss.2010.03.011. Epub 2010 Mar 31.
Increased expression of cyclooxygenase (COX-2) contributes to atherosclerosis. Recent studies suggest that COX-2 inhibitors prevent early plaque development but their effects on established lesions are less clear, while the statins promote plaque stability. The purpose of this study is to investigate whether administering a combination of a COX-2 inhibitor with a statin drug alters plaque progression in apo E-/- mice.
Apo E-/- mice were fed a Western diet from 6 to 26 wk of age. At 26 wk, the Western diets supplemented with atorvastatin, celecoxib, or atorvastatin plus celecoxib were given for an additional 12 wk.
When the mice were 38 wk of age, the total area occupied by the atherosclerotic lesion was 53% less in the mice fed the combination of atorvastatin + celecoxib P ≤ 0.05) than that of the apo E-/- mice fed the Western diet alone, atorvastatin alone, or celecoxib alone. The decreased extent of atherosclerosis observed in the apo E-/- mice fed the combination of drugs was associated with reduced levels of prostaglandin (PG) E(2,) decreased protein expression of metalloproteinase (MMP)-9, macrophage chemotactic protein (MCP-1), and COX 2, and decreased staining for MMP-9, F4-80 (a marker for macrophages), and vascular cell adhesion molecule (VCAM).
This study indicates that using statins with a COX-2 inhibitor reduced the extent of atherosclerosis and inflammatory/cell adhesion molecule levels in the apo E-/- mouse model.
环氧化酶(COX-2)表达增加有助于动脉粥样硬化的发生。最近的研究表明,COX-2 抑制剂可预防早期斑块形成,但它们对已形成的病变的作用尚不清楚,而他汀类药物则可促进斑块稳定。本研究旨在探讨 COX-2 抑制剂联合他汀类药物是否会改变载脂蛋白 E 基因缺失(apo E-/-)小鼠的斑块进展。
apo E-/- 小鼠从 6 至 26 周龄喂食西方饮食。在 26 周时,给予 apo E-/- 小鼠补充阿托伐他汀、塞来昔布或阿托伐他汀联合塞来昔布的西方饮食,持续 12 周。
当小鼠 38 周龄时,与单独喂食西方饮食、单独喂食阿托伐他汀或单独喂食塞来昔布的 apo E-/- 小鼠相比,喂食阿托伐他汀联合塞来昔布的小鼠的动脉粥样硬化病变总面积减少了 53%(P≤0.05)。在联合药物喂养的 apo E-/- 小鼠中观察到的动脉粥样硬化程度降低与前列腺素(PG)E2 水平降低、基质金属蛋白酶(MMP)-9、单核细胞趋化蛋白(MCP-1)和 COX-2 的蛋白表达降低以及 MMP-9、F4-80(巨噬细胞标志物)和血管细胞黏附分子(VCAM)染色减少有关。
本研究表明,在 apo E-/- 小鼠模型中,联合使用他汀类药物和 COX-2 抑制剂可减少动脉粥样硬化的程度和炎症/细胞黏附分子水平。