内膜增生
医学
再狭窄
结扎
新生内膜增生
增生
转基因小鼠
发病机制
颈动脉
血管成形术
病态的
基因剔除小鼠
病理
转基因
内科学
基因
支架
生物
平滑肌
生物化学
受体
作者
Le-Ning Zhang,John F. Parkinson,Christopher A. Haskell,Yixin Wang
标识
DOI:10.2174/157016108783331321
摘要
The murine carotid artery ligation (CAL) model has been widely used in the research of intimal hyperplasia, a major pathological process in vascular diseases, such as atherosclerosis and restenosis after angioplasty. Using a variety of gene knockout or transgenic mice and different pharmacological interventions, these studies have yielded significant new findings that contribute not only to unraveling the basic molecular mechanisms involved in the pathogenesis of intimal hyperplasia, but also to the identification of novel targets for intervention of these diseases. The current review outlines the findings derived from the murine CAL model, including studies run by the authors, covering the impacts of hyperlipidemia, pro-inflammatory factors, endothelial dysfunction, protease activity and growth mediators on neointimal hyperplasia.
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