Source:http://linkedlifedata.com/resource/pubmed/id/18482727
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
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pubmed:dateCreated |
2008-12-23
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pubmed:abstractText |
Recently, atherosclerosis has been considered to be the result of inflammation. Interestingly, hydroxymethylglutaryl-coenzyme (HMG-Co) A inhibitors (statins), which are clinically used as lipid-lowering agents, have been reported to have various anti-inflammatory effects. As abdominal aortic aneurysm (AAA) is a common degenerative condition associated with atherosclerosis, this study was designed to investigate the inhibitory effect of a statin, atorvastatin, on aneurysm formation apart from its lipid-lowering effect. We employed an elastase-induced rat AAA model, as statins do not lower cholesterol in rats. Mean aneurysm diameter was significantly smaller in the atorvastatin treatment group as compared to control at 4 weeks after surgery (P<0.05). Interestingly, atorvastatin inhibited the expression of ICAM and MCP-1, followed by the suppression of macrophage recruitment into the aortic wall at 1 week after operation. A significant reduction in MMP-12, but not MMP-2, -3 and -9, expression was also observed by treatment with atorvastatin at 1 week after surgery. In addition, synthesis of collagen and elastin in the vascular wall were significantly increased by atorvastatin. Here, the present study demonstrated a direct effect of atorvastatin to inhibit the progression of aortic aneurysm, independent of its lipid-lowering effect. This study suggests new therapeutic aspects of statins to inhibit the progression of aneurysms.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Anticholesteremic Agents,
http://linkedlifedata.com/resource/pubmed/chemical/Collagen,
http://linkedlifedata.com/resource/pubmed/chemical/Heptanoic Acids,
http://linkedlifedata.com/resource/pubmed/chemical/Hydroxymethylglutaryl-CoA...,
http://linkedlifedata.com/resource/pubmed/chemical/Pancreatic Elastase,
http://linkedlifedata.com/resource/pubmed/chemical/Pyrroles,
http://linkedlifedata.com/resource/pubmed/chemical/atorvastatin
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pubmed:status |
MEDLINE
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pubmed:month |
Jan
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pubmed:issn |
1879-1484
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:volume |
202
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
34-40
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pubmed:meshHeading |
pubmed-meshheading:18482727-Animals,
pubmed-meshheading:18482727-Anticholesteremic Agents,
pubmed-meshheading:18482727-Aortic Aneurysm, Abdominal,
pubmed-meshheading:18482727-Cell Movement,
pubmed-meshheading:18482727-Collagen,
pubmed-meshheading:18482727-Disease Models, Animal,
pubmed-meshheading:18482727-Heptanoic Acids,
pubmed-meshheading:18482727-Humans,
pubmed-meshheading:18482727-Hydroxymethylglutaryl-CoA Reductase Inhibitors,
pubmed-meshheading:18482727-Inflammation,
pubmed-meshheading:18482727-Macrophages,
pubmed-meshheading:18482727-Pancreatic Elastase,
pubmed-meshheading:18482727-Pyrroles,
pubmed-meshheading:18482727-Rats,
pubmed-meshheading:18482727-Rats, Wistar,
pubmed-meshheading:18482727-Treatment Outcome
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pubmed:year |
2009
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pubmed:articleTitle |
Inhibition of development of experimental aortic abdominal aneurysm in rat model by atorvastatin through inhibition of macrophage migration.
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pubmed:affiliation |
Division of Clinical Gene Therapy, Graduate School of Medicine, Osaka University, Suita, Japan.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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