Source:http://linkedlifedata.com/resource/pubmed/id/12740485
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
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pubmed:dateCreated |
2003-5-12
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pubmed:abstractText |
This study investigated the effect of pitavastatin, a 3-hydroxy-3-methylglutaryl coenzyme A ( HMG-CoA ) reductase inhibitor with strong cholesterol-lowering activity, on the composition of atherosclerotic plaque. Pitavastatin ( 0.5mg/kg ) was administered to Watanabe heritable hyperlipidemic ( WHHL ) rabbits for 16 weeks, with the result that plasma total cholesterol ( TC ), very low density lipoprotein ( VLDL )-C, intermediate density lipoprotein ( IDL )-C and low density lipoprotein ( LDL )-C decreased by 28.6, 60.0, 42.3 and 21.7%, respectively. In the aorta, pitavastatin reduced the area of the lesion by 38.6%. In the pitavastatin group, the macrophage-positive area in the aortic plaque was reduced by 39.4%, and the areas occupied by collagen and a-smooth muscle actin ( alpha-SMA )-positive area increased by 66.4 and 91.7%, respectively. In the aortic arch, pitavastatin increased the average thickness of alpha-SMA in the plaque by 96.7% and reduced the vulnerability index by 76.0%. Furthermore, pitavastatin reduced the positive areas of monocyte chemoattractant protein ( MCP )-1, matrix metalloproteinase ( MMP )-3 and MMP-9 by 39.1, 40.6 and 52.3%, respectively. These results indicated that pitavastatin had an excellent lipid-lowering effect in WHHL rabbits, suppressing the progression of atherosclerosis and stabilizing atherosclerotic plaque.
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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/Chemokine CCL2,
http://linkedlifedata.com/resource/pubmed/chemical/Hydroxymethylglutaryl-CoA...,
http://linkedlifedata.com/resource/pubmed/chemical/Lipoproteins,
http://linkedlifedata.com/resource/pubmed/chemical/Matrix Metalloproteinase 3,
http://linkedlifedata.com/resource/pubmed/chemical/Matrix Metalloproteinase 9,
http://linkedlifedata.com/resource/pubmed/chemical/Quinolines,
http://linkedlifedata.com/resource/pubmed/chemical/pitavastatin
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pubmed:status |
MEDLINE
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pubmed:issn |
1340-3478
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
10
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
109-16
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pubmed:dateRevised |
2010-11-18
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pubmed:meshHeading |
pubmed-meshheading:12740485-Animals,
pubmed-meshheading:12740485-Aorta,
pubmed-meshheading:12740485-Arteriosclerosis,
pubmed-meshheading:12740485-Chemokine CCL2,
pubmed-meshheading:12740485-Hydroxymethylglutaryl-CoA Reductase Inhibitors,
pubmed-meshheading:12740485-Hyperlipidemias,
pubmed-meshheading:12740485-Lipid Metabolism,
pubmed-meshheading:12740485-Lipoproteins,
pubmed-meshheading:12740485-Matrix Metalloproteinase 3,
pubmed-meshheading:12740485-Matrix Metalloproteinase 9,
pubmed-meshheading:12740485-Quinolines,
pubmed-meshheading:12740485-Rabbits
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pubmed:year |
2003
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pubmed:articleTitle |
Plaque-stabilizing effect of pitavastatin in Watanabe heritable hyperlipidemic (WHHL) rabbits.
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pubmed:affiliation |
Tokyo New Drug Research Laboratories I, Pharmaceutical Division, Kowa Co. Ltd, 2-17-43 Noguchi-cho, Higashi-murayama, Tokyo 189-0022, Japan. h-suzuki@kowa.co.jp
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pubmed:publicationType |
Journal Article,
Evaluation Studies
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