2009
DOI: 10.1016/j.atherosclerosis.2008.11.013
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Rosuvastatin reduces atherosclerotic lesions and promotes progenitor cell mobilisation and recruitment in apolipoprotein E knockout mice

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Cited by 25 publications
(17 citation statements)
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“…Other statins studied included fluvastatin (12%, 6/49), lovastatin or rosuvastatin (8%, 4/49), and cerivastatin or pitavastatin (6%, 3/49). Of the 63 studies, five studies [22][26] evaluated multiple statins, of which four were included in the meta-analysis [22][24],[26].…”
Section: Resultsmentioning
confidence: 99%
“…Other statins studied included fluvastatin (12%, 6/49), lovastatin or rosuvastatin (8%, 4/49), and cerivastatin or pitavastatin (6%, 3/49). Of the 63 studies, five studies [22][26] evaluated multiple statins, of which four were included in the meta-analysis [22][24],[26].…”
Section: Resultsmentioning
confidence: 99%
“…Atherogenesis is also regulated by PI3K/Akt pathway. Statins induce their activation on vascular and immune cells, thus, reducing atherosclerotic lesions in ApoE knockout mice [208] and endothelial dysfunction in type 2 diabetic mice [209]. Controversial results on statin-mediated MAPK phosphorylation have been showed.…”
Section: Statin-mediated Activation Of Intracellular Pathwaysmentioning
confidence: 99%
“…Statins induce a robust mobilization of murine CD117+/Sca-1+ progenitor cells and EPCs via the PI3K/Akt pathways and enhance endothelialization of injured vessels thereby leading to attenuation of neointimal formation [7][10]. Moreover, recent clinical trials show an LDL-independent superiority of intensive compared to moderate statin therapy in reducing target vessel revascularization in patients who undergo PCI for acute coronary syndromes [11].…”
Section: Introductionmentioning
confidence: 99%