Effects of aspirin on atherosclerosis and the cyclooxygenase-2 expression in atherosclerotic rabbits

Background Atherosclerosis is a complex vascular inflammatory disease. Aspirin is a mainstay in the prevention of vascular complications of atherosclerosis. In this study, the effectiveness of aspirin in suppressing atherosclerosis and the inflammation process was evaluated in rabbits fed with a hig...

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Veröffentlicht in:Chinese medical journal 2006-11, Vol.119 (21), p.1808-1814
Hauptverfasser: Guo, Yi, Wang, Qi-zhang, Tang, Bing-shan, Zuo, Yan-fang, Li, Fang-ming, Jiang, Xin, Wang, Ling, Ma, Ke-fu
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container_end_page 1814
container_issue 21
container_start_page 1808
container_title Chinese medical journal
container_volume 119
creator Guo, Yi
Wang, Qi-zhang
Tang, Bing-shan
Zuo, Yan-fang
Li, Fang-ming
Jiang, Xin
Wang, Ling
Ma, Ke-fu
description Background Atherosclerosis is a complex vascular inflammatory disease. Aspirin is a mainstay in the prevention of vascular complications of atherosclerosis. In this study, the effectiveness of aspirin in suppressing atherosclerosis and the inflammation process was evaluated in rabbits fed with a high fat diet. Methods Eighteen male New Zealand rabbits were randomly divided into 3 groups: control group, untreated cholesterol-fed group, aspirin treated cholesterol-fed group, which were fed for 12 weeks. After 12 weeks, the aorta was harvested for pathologic morphology observation. Immunohistochemical analysis of cyclooxygenase-2 (COX-2), macrophage and vascular smooth muscle cell (VSMC) was performed. The statistical analysis was performed by the statistical program SPSS 10.0. Results The aorta plaque/intima size (P/I) by pathologic morphology observation was 0%, (59.6± 13.7)% and (36.3±16.5)% in the control, untreated cholesterol-fed group and aspirin treated group, respectively. The maximum plaque thickness, the degree of artery stenosis and the proportion of the intimal circumference occupied by atheroma of the 3 groups were significantly different from each other (P〈0.01). The expression of COX-2 and macrophage in plaque of the aspirin treated group were decreased compared with that in untreated cholesterol-fed group. However, no difference was found in the expression of VSMC between the aspirin treated and the untreated cholesterol-fed group. Conclusion The mechanism of atherosclerosis suppression by aspirin in cholesterol-fed rabbits is related to the inhibition of COX-2 expression together with the reduced inflammation followed by, but not related to the hypolipidemic effects.
doi_str_mv 10.1097/00029330-200611010-00008
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Aspirin is a mainstay in the prevention of vascular complications of atherosclerosis. In this study, the effectiveness of aspirin in suppressing atherosclerosis and the inflammation process was evaluated in rabbits fed with a high fat diet. Methods Eighteen male New Zealand rabbits were randomly divided into 3 groups: control group, untreated cholesterol-fed group, aspirin treated cholesterol-fed group, which were fed for 12 weeks. After 12 weeks, the aorta was harvested for pathologic morphology observation. Immunohistochemical analysis of cyclooxygenase-2 (COX-2), macrophage and vascular smooth muscle cell (VSMC) was performed. The statistical analysis was performed by the statistical program SPSS 10.0. Results The aorta plaque/intima size (P/I) by pathologic morphology observation was 0%, (59.6± 13.7)% and (36.3±16.5)% in the control, untreated cholesterol-fed group and aspirin treated group, respectively. The maximum plaque thickness, the degree of artery stenosis and the proportion of the intimal circumference occupied by atheroma of the 3 groups were significantly different from each other (P〈0.01). The expression of COX-2 and macrophage in plaque of the aspirin treated group were decreased compared with that in untreated cholesterol-fed group. However, no difference was found in the expression of VSMC between the aspirin treated and the untreated cholesterol-fed group. Conclusion The mechanism of atherosclerosis suppression by aspirin in cholesterol-fed rabbits is related to the inhibition of COX-2 expression together with the reduced inflammation followed by, but not related to the hypolipidemic effects.</description><identifier>ISSN: 0366-6999</identifier><identifier>EISSN: 2542-5641</identifier><identifier>DOI: 10.1097/00029330-200611010-00008</identifier><identifier>PMID: 17097036</identifier><language>eng</language><publisher>China: Department of Neurology, Second Affiliated Hospital of Jinan University, Shenzhen 518020, China%Department of Neurology, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, China</publisher><subject>Animals ; Aorta - pathology ; Aspirin - pharmacology ; Atherosclerosis - pathology ; Atherosclerosis - prevention &amp; control ; Cholesterol, Dietary - administration &amp; dosage ; Cyclooxygenase 2 - analysis ; Immunohistochemistry ; Lipids - blood ; Male ; Rabbits ; 动脉硬化症 ; 环氧合酶-2 ; 病理机制 ; 阿斯匹林</subject><ispartof>Chinese medical journal, 2006-11, Vol.119 (21), p.1808-1814</ispartof><rights>Copyright © Wanfang Data Co. Ltd. All Rights Reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c421t-712d1e1617041aa4291bd0474c29a2634ec2d5a6dc37eef9b55f83e9016733453</citedby><cites>FETCH-LOGICAL-c421t-712d1e1617041aa4291bd0474c29a2634ec2d5a6dc37eef9b55f83e9016733453</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://image.cqvip.com/vip1000/qk/85656X/85656X.jpg</thumbnail><link.rule.ids>314,780,784,864,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17097036$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Guo, Yi</creatorcontrib><creatorcontrib>Wang, Qi-zhang</creatorcontrib><creatorcontrib>Tang, Bing-shan</creatorcontrib><creatorcontrib>Zuo, Yan-fang</creatorcontrib><creatorcontrib>Li, Fang-ming</creatorcontrib><creatorcontrib>Jiang, Xin</creatorcontrib><creatorcontrib>Wang, Ling</creatorcontrib><creatorcontrib>Ma, Ke-fu</creatorcontrib><title>Effects of aspirin on atherosclerosis and the cyclooxygenase-2 expression in atherosclerotic rabbits</title><title>Chinese medical journal</title><addtitle>Chinese Medical Journal</addtitle><description>Background Atherosclerosis is a complex vascular inflammatory disease. Aspirin is a mainstay in the prevention of vascular complications of atherosclerosis. In this study, the effectiveness of aspirin in suppressing atherosclerosis and the inflammation process was evaluated in rabbits fed with a high fat diet. Methods Eighteen male New Zealand rabbits were randomly divided into 3 groups: control group, untreated cholesterol-fed group, aspirin treated cholesterol-fed group, which were fed for 12 weeks. After 12 weeks, the aorta was harvested for pathologic morphology observation. Immunohistochemical analysis of cyclooxygenase-2 (COX-2), macrophage and vascular smooth muscle cell (VSMC) was performed. The statistical analysis was performed by the statistical program SPSS 10.0. Results The aorta plaque/intima size (P/I) by pathologic morphology observation was 0%, (59.6± 13.7)% and (36.3±16.5)% in the control, untreated cholesterol-fed group and aspirin treated group, respectively. The maximum plaque thickness, the degree of artery stenosis and the proportion of the intimal circumference occupied by atheroma of the 3 groups were significantly different from each other (P〈0.01). The expression of COX-2 and macrophage in plaque of the aspirin treated group were decreased compared with that in untreated cholesterol-fed group. However, no difference was found in the expression of VSMC between the aspirin treated and the untreated cholesterol-fed group. Conclusion The mechanism of atherosclerosis suppression by aspirin in cholesterol-fed rabbits is related to the inhibition of COX-2 expression together with the reduced inflammation followed by, but not related to the hypolipidemic effects.</description><subject>Animals</subject><subject>Aorta - pathology</subject><subject>Aspirin - pharmacology</subject><subject>Atherosclerosis - pathology</subject><subject>Atherosclerosis - prevention &amp; control</subject><subject>Cholesterol, Dietary - administration &amp; dosage</subject><subject>Cyclooxygenase 2 - analysis</subject><subject>Immunohistochemistry</subject><subject>Lipids - blood</subject><subject>Male</subject><subject>Rabbits</subject><subject>动脉硬化症</subject><subject>环氧合酶-2</subject><subject>病理机制</subject><subject>阿斯匹林</subject><issn>0366-6999</issn><issn>2542-5641</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVUcFOGzEQtVARBMovVFYPvS14bK83PlaIAhJSL3C2vN5x4rCxg71RCV9fp6RFvcxI4_fejN8jhAK7BKa7K8YY10KwhjOmABiwpo7Y_IjMeCt50yoJn8iMCaUapbU-JWelrCqpbTt1Qk6hqyr1dUaGG-_RTYUmT23ZhBwiTZHaaYk5FTfuayjUxoHWEXU7N6b0ultgtAUbTvF1k7GUUDnhf9oUHM2278NUPpNjb8eCF4d-Tp5-3Dxe3zUPP2_vr78_NE5ymJoO-AAIql4nwVrJNfQDk510XFuuhETHh9aqwYkO0eu-bf1coGagOiFkK87Jt3fdXzZ6GxdmlbY51o3mbenWq71ZHKpNH8BNTi9bLJNZh-JwHG3EtC1GzUFIJXgFzt-Brn6rZPRmk8Pa5p0BZvZRmL9RmH9RmD9RVOqXw45tv8bhg3jwvgK-HrSXKS5eQr23t-7ZhxENF9ApxoX4DapQj38</recordid><startdate>20061105</startdate><enddate>20061105</enddate><creator>Guo, Yi</creator><creator>Wang, Qi-zhang</creator><creator>Tang, Bing-shan</creator><creator>Zuo, Yan-fang</creator><creator>Li, Fang-ming</creator><creator>Jiang, Xin</creator><creator>Wang, Ling</creator><creator>Ma, Ke-fu</creator><general>Department of Neurology, Second Affiliated Hospital of Jinan University, Shenzhen 518020, China%Department of Neurology, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, China</general><scope>2RA</scope><scope>92L</scope><scope>CQIGP</scope><scope>W91</scope><scope>~WA</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>2B.</scope><scope>4A8</scope><scope>92I</scope><scope>93N</scope><scope>PSX</scope><scope>TCJ</scope></search><sort><creationdate>20061105</creationdate><title>Effects of aspirin on atherosclerosis and the cyclooxygenase-2 expression in atherosclerotic rabbits</title><author>Guo, Yi ; Wang, Qi-zhang ; Tang, Bing-shan ; Zuo, Yan-fang ; Li, Fang-ming ; Jiang, Xin ; Wang, Ling ; Ma, Ke-fu</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c421t-712d1e1617041aa4291bd0474c29a2634ec2d5a6dc37eef9b55f83e9016733453</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Animals</topic><topic>Aorta - pathology</topic><topic>Aspirin - pharmacology</topic><topic>Atherosclerosis - pathology</topic><topic>Atherosclerosis - prevention &amp; control</topic><topic>Cholesterol, Dietary - administration &amp; dosage</topic><topic>Cyclooxygenase 2 - analysis</topic><topic>Immunohistochemistry</topic><topic>Lipids - blood</topic><topic>Male</topic><topic>Rabbits</topic><topic>动脉硬化症</topic><topic>环氧合酶-2</topic><topic>病理机制</topic><topic>阿斯匹林</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Guo, Yi</creatorcontrib><creatorcontrib>Wang, Qi-zhang</creatorcontrib><creatorcontrib>Tang, Bing-shan</creatorcontrib><creatorcontrib>Zuo, Yan-fang</creatorcontrib><creatorcontrib>Li, Fang-ming</creatorcontrib><creatorcontrib>Jiang, Xin</creatorcontrib><creatorcontrib>Wang, Ling</creatorcontrib><creatorcontrib>Ma, Ke-fu</creatorcontrib><collection>中文科技期刊数据库</collection><collection>中文科技期刊数据库-CALIS站点</collection><collection>中文科技期刊数据库-7.0平台</collection><collection>中文科技期刊数据库-医药卫生</collection><collection>中文科技期刊数据库- 镜像站点</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Wanfang Data Journals - Hong Kong</collection><collection>WANFANG Data Centre</collection><collection>Wanfang Data Journals</collection><collection>万方数据期刊 - 香港版</collection><collection>China Online Journals (COJ)</collection><collection>China Online Journals (COJ)</collection><jtitle>Chinese medical journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Guo, Yi</au><au>Wang, Qi-zhang</au><au>Tang, Bing-shan</au><au>Zuo, Yan-fang</au><au>Li, Fang-ming</au><au>Jiang, Xin</au><au>Wang, Ling</au><au>Ma, Ke-fu</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effects of aspirin on atherosclerosis and the cyclooxygenase-2 expression in atherosclerotic rabbits</atitle><jtitle>Chinese medical journal</jtitle><addtitle>Chinese Medical Journal</addtitle><date>2006-11-05</date><risdate>2006</risdate><volume>119</volume><issue>21</issue><spage>1808</spage><epage>1814</epage><pages>1808-1814</pages><issn>0366-6999</issn><eissn>2542-5641</eissn><abstract>Background Atherosclerosis is a complex vascular inflammatory disease. Aspirin is a mainstay in the prevention of vascular complications of atherosclerosis. In this study, the effectiveness of aspirin in suppressing atherosclerosis and the inflammation process was evaluated in rabbits fed with a high fat diet. Methods Eighteen male New Zealand rabbits were randomly divided into 3 groups: control group, untreated cholesterol-fed group, aspirin treated cholesterol-fed group, which were fed for 12 weeks. After 12 weeks, the aorta was harvested for pathologic morphology observation. Immunohistochemical analysis of cyclooxygenase-2 (COX-2), macrophage and vascular smooth muscle cell (VSMC) was performed. The statistical analysis was performed by the statistical program SPSS 10.0. Results The aorta plaque/intima size (P/I) by pathologic morphology observation was 0%, (59.6± 13.7)% and (36.3±16.5)% in the control, untreated cholesterol-fed group and aspirin treated group, respectively. The maximum plaque thickness, the degree of artery stenosis and the proportion of the intimal circumference occupied by atheroma of the 3 groups were significantly different from each other (P〈0.01). The expression of COX-2 and macrophage in plaque of the aspirin treated group were decreased compared with that in untreated cholesterol-fed group. However, no difference was found in the expression of VSMC between the aspirin treated and the untreated cholesterol-fed group. Conclusion The mechanism of atherosclerosis suppression by aspirin in cholesterol-fed rabbits is related to the inhibition of COX-2 expression together with the reduced inflammation followed by, but not related to the hypolipidemic effects.</abstract><cop>China</cop><pub>Department of Neurology, Second Affiliated Hospital of Jinan University, Shenzhen 518020, China%Department of Neurology, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, China</pub><pmid>17097036</pmid><doi>10.1097/00029330-200611010-00008</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record>
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subjects Animals
Aorta - pathology
Aspirin - pharmacology
Atherosclerosis - pathology
Atherosclerosis - prevention & control
Cholesterol, Dietary - administration & dosage
Cyclooxygenase 2 - analysis
Immunohistochemistry
Lipids - blood
Male
Rabbits
动脉硬化症
环氧合酶-2
病理机制
阿斯匹林
title Effects of aspirin on atherosclerosis and the cyclooxygenase-2 expression in atherosclerotic rabbits
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