Severity of Hyperlipidemia Does Not Affect Antiatherosclerotic Effect of an Angiotensin II Receptor Antagonist in Apolipoprotein E-deficient Mice
The purpose of this study was to clarify whether severity of hyperlipidemia affects the antiatherosclerotic effect of angiotensin II receptor blockers (ARBs). The effect of olmesartan medoxomil, an ARB, on atherosclerotic lesion was examined in apolipoprotein E-deficient (ApoEKO) mice fed a normal d...
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Veröffentlicht in: | Journal of cardiovascular pharmacology 2006-06, Vol.47 (6), p.764-769 |
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creator | Kato, Mikio Sada, Toshio Chuma, Hiroko Mizuno, Makoto Terashima, Hideki Fukushima, Yasuo Koike, Hiroyuki |
description | The purpose of this study was to clarify whether severity of hyperlipidemia affects the antiatherosclerotic effect of angiotensin II receptor blockers (ARBs). The effect of olmesartan medoxomil, an ARB, on atherosclerotic lesion was examined in apolipoprotein E-deficient (ApoEKO) mice fed a normal diet (ND) or a high-fat–supplemented diet (FD) for 25 weeks. ApoEKO mice have high plasma cholesterol levels, which were further increased by feeding of an FD. Both the atherosclerotic lesion area of the aortic luminal surface and the atherosclerotic lesion thickness in the aortic valves were significantly greater in the FD mice than in the ND mice. Olmesartan medoxomil did not affect the plasma cholesterol levels in either the ND or FD ApoEKO mice; however, it reduced effectively both the atherosclerotic lesion surface area and the lesion thickness even in FD ApoEKO mice. It is concluded that the antiatherosclerotic effect of ARBs is not weakened by the high plasma cholesterol level, suggesting the usefulness of ARBs in the treatment of atherosclerosis, even in a situation in which the plasma cholesterol level is not fully controlled. |
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The effect of olmesartan medoxomil, an ARB, on atherosclerotic lesion was examined in apolipoprotein E-deficient (ApoEKO) mice fed a normal diet (ND) or a high-fat–supplemented diet (FD) for 25 weeks. ApoEKO mice have high plasma cholesterol levels, which were further increased by feeding of an FD. Both the atherosclerotic lesion area of the aortic luminal surface and the atherosclerotic lesion thickness in the aortic valves were significantly greater in the FD mice than in the ND mice. Olmesartan medoxomil did not affect the plasma cholesterol levels in either the ND or FD ApoEKO mice; however, it reduced effectively both the atherosclerotic lesion surface area and the lesion thickness even in FD ApoEKO mice. It is concluded that the antiatherosclerotic effect of ARBs is not weakened by the high plasma cholesterol level, suggesting the usefulness of ARBs in the treatment of atherosclerosis, even in a situation in which the plasma cholesterol level is not fully controlled.</description><identifier>ISSN: 0160-2446</identifier><identifier>EISSN: 1533-4023</identifier><identifier>DOI: 10.1097/01.fjc.0000211788.37658.ad</identifier><identifier>PMID: 16810077</identifier><language>eng</language><publisher>United States: Lippincott Williams & Wilkins, Inc</publisher><subject>Angiotensin II Type 1 Receptor Blockers - pharmacology ; Angiotensin II Type 1 Receptor Blockers - therapeutic use ; Animals ; Aorta - pathology ; Aortic Valve - pathology ; Apolipoproteins E - deficiency ; Atherosclerosis - blood ; Atherosclerosis - drug therapy ; Atherosclerosis - pathology ; Blood Pressure ; Cholesterol - blood ; Heart Rate ; Hyperlipidemias - physiopathology ; Imidazoles - pharmacology ; Imidazoles - therapeutic use ; Male ; Mice ; Mice, Inbred C57BL ; Olmesartan Medoxomil ; Tetrazoles - pharmacology ; Tetrazoles - therapeutic use ; Triglycerides - blood</subject><ispartof>Journal of cardiovascular pharmacology, 2006-06, Vol.47 (6), p.764-769</ispartof><rights>2006 Lippincott Williams & Wilkins, Inc.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3297-84b626d75586b6fc121ad31d86d17f2bf8f5b85b1b3c29606bb03fb194174b83</citedby><cites>FETCH-LOGICAL-c3297-84b626d75586b6fc121ad31d86d17f2bf8f5b85b1b3c29606bb03fb194174b83</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf><![CDATA[$$Uhttp://ovidsp.ovid.com/ovidweb.cgi?T=JS&CSC=Y&NEWS=N&PAGE=fulltext&PDF=y&D=ovft&AN=00005344-200606000-00007$$EPDF$$P50$$Gwolterskluwer$$H]]></linktopdf><linktohtml>$$Uhttp://ovidsp.ovid.com/ovidweb.cgi?T=JS&NEWS=n&CSC=Y&PAGE=fulltext&D=ovft&AN=00005344-200606000-00007$$EHTML$$P50$$Gwolterskluwer$$H</linktohtml><link.rule.ids>315,781,785,4610,27929,27930,64671,65466</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16810077$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kato, Mikio</creatorcontrib><creatorcontrib>Sada, Toshio</creatorcontrib><creatorcontrib>Chuma, Hiroko</creatorcontrib><creatorcontrib>Mizuno, Makoto</creatorcontrib><creatorcontrib>Terashima, Hideki</creatorcontrib><creatorcontrib>Fukushima, Yasuo</creatorcontrib><creatorcontrib>Koike, Hiroyuki</creatorcontrib><title>Severity of Hyperlipidemia Does Not Affect Antiatherosclerotic Effect of an Angiotensin II Receptor Antagonist in Apolipoprotein E-deficient Mice</title><title>Journal of cardiovascular pharmacology</title><addtitle>J Cardiovasc Pharmacol</addtitle><description>The purpose of this study was to clarify whether severity of hyperlipidemia affects the antiatherosclerotic effect of angiotensin II receptor blockers (ARBs). The effect of olmesartan medoxomil, an ARB, on atherosclerotic lesion was examined in apolipoprotein E-deficient (ApoEKO) mice fed a normal diet (ND) or a high-fat–supplemented diet (FD) for 25 weeks. ApoEKO mice have high plasma cholesterol levels, which were further increased by feeding of an FD. Both the atherosclerotic lesion area of the aortic luminal surface and the atherosclerotic lesion thickness in the aortic valves were significantly greater in the FD mice than in the ND mice. Olmesartan medoxomil did not affect the plasma cholesterol levels in either the ND or FD ApoEKO mice; however, it reduced effectively both the atherosclerotic lesion surface area and the lesion thickness even in FD ApoEKO mice. It is concluded that the antiatherosclerotic effect of ARBs is not weakened by the high plasma cholesterol level, suggesting the usefulness of ARBs in the treatment of atherosclerosis, even in a situation in which the plasma cholesterol level is not fully controlled.</description><subject>Angiotensin II Type 1 Receptor Blockers - pharmacology</subject><subject>Angiotensin II Type 1 Receptor Blockers - therapeutic use</subject><subject>Animals</subject><subject>Aorta - pathology</subject><subject>Aortic Valve - pathology</subject><subject>Apolipoproteins E - deficiency</subject><subject>Atherosclerosis - blood</subject><subject>Atherosclerosis - drug therapy</subject><subject>Atherosclerosis - pathology</subject><subject>Blood Pressure</subject><subject>Cholesterol - blood</subject><subject>Heart Rate</subject><subject>Hyperlipidemias - physiopathology</subject><subject>Imidazoles - pharmacology</subject><subject>Imidazoles - therapeutic use</subject><subject>Male</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Olmesartan Medoxomil</subject><subject>Tetrazoles - pharmacology</subject><subject>Tetrazoles - therapeutic use</subject><subject>Triglycerides - blood</subject><issn>0160-2446</issn><issn>1533-4023</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFUcFuEzEQtRCIpoFfQBYHbru1117byy1qA41UQILeLds7blw262XtUOUz-GOcJlJ98Ghm3nszo4fQR0pqSjp5RWjtH11NymsolUrVTIpW1aZ_hRa0ZazipGGv0YJQQaqGc3GBLlN6JITyVoq36IIKRQmRcoH-_YK_MId8wNHj28ME8xCm0MMuGHwTIeHvMeOV9-BKGHMweQtzTG4ofw4Or0-tQjZjATyEmGFMYcSbDf4JDqYc5yPRPMQxpIxLZzXFMiNORQBKuq568MEFGDP-Fhy8Q2-8GRK8P8cluv-yvr--re5-fN1cr-4qx5pOVopb0Yhetq0SVnhHG2p6Rnsleip9Y73yrVWtpZa5phNEWEuYt7TjVHKr2BJ9OsmWPf7sIWW9C8nBMJgR4j5podqOcU4K8PMJ6MrdaQavpznszHzQlOijH5pQXfzQL37oZz902WeJPpyn7O0O-hfq2YAC4CfAUxwyzOn3sH-CWW_BDHn7LNmWLaqGkHJCyapjSbL_6ryZkw</recordid><startdate>200606</startdate><enddate>200606</enddate><creator>Kato, Mikio</creator><creator>Sada, Toshio</creator><creator>Chuma, Hiroko</creator><creator>Mizuno, Makoto</creator><creator>Terashima, Hideki</creator><creator>Fukushima, Yasuo</creator><creator>Koike, Hiroyuki</creator><general>Lippincott Williams & Wilkins, Inc</general><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></search><sort><creationdate>200606</creationdate><title>Severity of Hyperlipidemia Does Not Affect Antiatherosclerotic Effect of an Angiotensin II Receptor Antagonist in Apolipoprotein E-deficient Mice</title><author>Kato, Mikio ; Sada, Toshio ; Chuma, Hiroko ; Mizuno, Makoto ; Terashima, Hideki ; Fukushima, Yasuo ; Koike, Hiroyuki</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3297-84b626d75586b6fc121ad31d86d17f2bf8f5b85b1b3c29606bb03fb194174b83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Angiotensin II Type 1 Receptor Blockers - pharmacology</topic><topic>Angiotensin II Type 1 Receptor Blockers - therapeutic use</topic><topic>Animals</topic><topic>Aorta - pathology</topic><topic>Aortic Valve - pathology</topic><topic>Apolipoproteins E - deficiency</topic><topic>Atherosclerosis - blood</topic><topic>Atherosclerosis - drug therapy</topic><topic>Atherosclerosis - pathology</topic><topic>Blood Pressure</topic><topic>Cholesterol - blood</topic><topic>Heart Rate</topic><topic>Hyperlipidemias - physiopathology</topic><topic>Imidazoles - pharmacology</topic><topic>Imidazoles - therapeutic use</topic><topic>Male</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Olmesartan Medoxomil</topic><topic>Tetrazoles - pharmacology</topic><topic>Tetrazoles - therapeutic use</topic><topic>Triglycerides - blood</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kato, Mikio</creatorcontrib><creatorcontrib>Sada, Toshio</creatorcontrib><creatorcontrib>Chuma, Hiroko</creatorcontrib><creatorcontrib>Mizuno, Makoto</creatorcontrib><creatorcontrib>Terashima, Hideki</creatorcontrib><creatorcontrib>Fukushima, Yasuo</creatorcontrib><creatorcontrib>Koike, Hiroyuki</creatorcontrib><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><jtitle>Journal of cardiovascular pharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kato, Mikio</au><au>Sada, Toshio</au><au>Chuma, Hiroko</au><au>Mizuno, Makoto</au><au>Terashima, Hideki</au><au>Fukushima, Yasuo</au><au>Koike, Hiroyuki</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Severity of Hyperlipidemia Does Not Affect Antiatherosclerotic Effect of an Angiotensin II Receptor Antagonist in Apolipoprotein E-deficient Mice</atitle><jtitle>Journal of cardiovascular pharmacology</jtitle><addtitle>J Cardiovasc Pharmacol</addtitle><date>2006-06</date><risdate>2006</risdate><volume>47</volume><issue>6</issue><spage>764</spage><epage>769</epage><pages>764-769</pages><issn>0160-2446</issn><eissn>1533-4023</eissn><abstract>The purpose of this study was to clarify whether severity of hyperlipidemia affects the antiatherosclerotic effect of angiotensin II receptor blockers (ARBs). The effect of olmesartan medoxomil, an ARB, on atherosclerotic lesion was examined in apolipoprotein E-deficient (ApoEKO) mice fed a normal diet (ND) or a high-fat–supplemented diet (FD) for 25 weeks. ApoEKO mice have high plasma cholesterol levels, which were further increased by feeding of an FD. Both the atherosclerotic lesion area of the aortic luminal surface and the atherosclerotic lesion thickness in the aortic valves were significantly greater in the FD mice than in the ND mice. Olmesartan medoxomil did not affect the plasma cholesterol levels in either the ND or FD ApoEKO mice; however, it reduced effectively both the atherosclerotic lesion surface area and the lesion thickness even in FD ApoEKO mice. It is concluded that the antiatherosclerotic effect of ARBs is not weakened by the high plasma cholesterol level, suggesting the usefulness of ARBs in the treatment of atherosclerosis, even in a situation in which the plasma cholesterol level is not fully controlled.</abstract><cop>United States</cop><pub>Lippincott Williams & Wilkins, Inc</pub><pmid>16810077</pmid><doi>10.1097/01.fjc.0000211788.37658.ad</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Angiotensin II Type 1 Receptor Blockers - pharmacology Angiotensin II Type 1 Receptor Blockers - therapeutic use Animals Aorta - pathology Aortic Valve - pathology Apolipoproteins E - deficiency Atherosclerosis - blood Atherosclerosis - drug therapy Atherosclerosis - pathology Blood Pressure Cholesterol - blood Heart Rate Hyperlipidemias - physiopathology Imidazoles - pharmacology Imidazoles - therapeutic use Male Mice Mice, Inbred C57BL Olmesartan Medoxomil Tetrazoles - pharmacology Tetrazoles - therapeutic use Triglycerides - blood |
title | Severity of Hyperlipidemia Does Not Affect Antiatherosclerotic Effect of an Angiotensin II Receptor Antagonist in Apolipoprotein E-deficient Mice |
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