| Literature DB >> 26445800 |
Yung Chih Chen1,2, Jennifer Rivera1, Karlheinz Peter3,4.
Abstract
Despite the number of animal models of atherosclerosis, a major limitation in research on mechanisms of plaque rupture is the lack of appropriate atherosclerotic mouse models where lesions develop and progress to a vulnerable and thus rupture-prone phenotype that is typically observed in humans. Most animal models of atherosclerosis typically represent a few but not the full combination of the characteristics seen in human unstable/ruptured plaques. Such characteristics most importantly include a thin and ruptured fibrous cap, plaque inflammation, neovascularization within the plaque (vasa vasorum), plaque hemorrhage, and intravascular (often occlusive) thrombus formation. Ideally, an animal model of plaque instability/rupture would respond to current pharmacological interventions known to reduce the risk of plaque rupture, such as statins. Here we describe a mouse model of plaque instability/rupture that is based on the surgical introduction of a tandem stenosis in the carotid artery. This model results in the formation of unstable atherosclerotic plaques that reflect human plaque pathology. It will allow to further understanding of plaque instability/rupture, to identify the participating factors such as specific proteins, genes and microRNAs, and to develop imaging methods towards the detection of vulnerable, rupture-prone atherosclerotic plaques.Entities:
Keywords: Acute myocardial infarction; Angiogenesis animal models of human disease; Arterial thrombosis; Atherosclerosis; Gene expression profiling; Inflammation; MicroRNA profiling; Plaque rupture
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Year: 2015 PMID: 26445800 DOI: 10.1007/978-1-4939-2929-0_23
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745