Focal histopathological progression of porcine experimental abdominal aortic aneurysm is mitigated by atorvastatin
Language English Country Italy Media print
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
23711681
PII: R34Y2013N03A0291
Knihovny.cz E-resources
- MeSH
- Aortic Aneurysm, Abdominal chemically induced diagnostic imaging pathology prevention & control MeSH
- Aorta, Abdominal diagnostic imaging drug effects pathology MeSH
- Atorvastatin MeSH
- Time Factors MeSH
- Heptanoic Acids pharmacology MeSH
- Disease Models, Animal MeSH
- Pancreatic Elastase MeSH
- Disease Progression MeSH
- Pyrroles pharmacology MeSH
- Hydroxymethylglutaryl-CoA Reductase Inhibitors pharmacology MeSH
- Sus scrofa MeSH
- Ultrasonography MeSH
- Animals MeSH
- Check Tag
- Female MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Atorvastatin MeSH
- Heptanoic Acids MeSH
- Pancreatic Elastase MeSH
- Pyrroles MeSH
- Hydroxymethylglutaryl-CoA Reductase Inhibitors MeSH
AIM: Observational studies in human patients and animal experiments suggested that statins have a potential in slowing the growth of small abdominal aortic aneurysms (AAA). Our aim was to quantify histological postoperative changes of AAA in porcine experimental model of AAA with and without administration of atorvastatin. METHODS: The AAA was induced by intraaortic infusion of porcine pancreatic elastase and subrenal application of plastic cuff. The AAA statin group (N.=14) received atorvastatin 1 mg/kg daily for 28 days, the other AAA group (N.=13) did not. The aortic diameter was measured by ultrasonography. Aortic samples were described using eleven quantitative histological parameters and compared with healthy aortae. RESULTS: There was no difference in aortic diameter between the AAA with statin when compared to AAA without statin. Administration of atorvastatin led to a better postoperative histological condition of the aortic elastin network, preservation of contractile phenotype of vascular smooth muscle, a higher density of vasa vasorum, it prevented thickening of intima and media. The increase in wall thickness in AAA without atorvastatin has not been accompanied by a proportional increase in number of vasa vasorum. CONCLUSION: The effects of atorvastatin seem to prevent the histopathological progression of AAA.