Radiation-Induced Atherosclerotic Plaque Progression in a Hypercholesterolemic Rabbit: A Prospective Vulnerable Plaque Model?

Human observations provide rich soil for making hypotheses, but good animal models are essential for understanding the disease and to test treatment modalities. Currently, there is no standard animal model of vulnerable plaque; therefore, the purpose of this study is to develop a pathophysiologicall...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Cardiovascular radiation medicine 2003-07, Vol.4 (3), p.146-151
Hauptverfasser: Pakala, Rajbabu, Leborgne, Laurent, Cheneau, Edouard, Chan, Rosanna C., Yazdi, Hamid, Fournadjiev, Jana, Weber, Deena, Hellinga, David, Kolodgie, Frank, Virmani, Renu, Waksman, Ron
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 151
container_issue 3
container_start_page 146
container_title Cardiovascular radiation medicine
container_volume 4
creator Pakala, Rajbabu
Leborgne, Laurent
Cheneau, Edouard
Chan, Rosanna C.
Yazdi, Hamid
Fournadjiev, Jana
Weber, Deena
Hellinga, David
Kolodgie, Frank
Virmani, Renu
Waksman, Ron
description Human observations provide rich soil for making hypotheses, but good animal models are essential for understanding the disease and to test treatment modalities. Currently, there is no standard animal model of vulnerable plaque; therefore, the purpose of this study is to develop a pathophysiologically relevant vulnerable plaque model. New Zealand White rabbits were fed with 1% hypercholesterolemic (HC) diet for 7 days, followed by balloon denudation of both the iliac arteries, and continued on 1% HC diet. Four weeks later, in 12 rabbits one of the iliac arteries was radiated (192-Ir, 15 Gy), and in five rabbits both the iliac arteries were sham treated. Following that, rabbits were fed with 0.15% HC diet. Four weeks later, arteries were processed for histomorphometry or immunohistochemistry. Serum cholesterol levels were similar in all the groups. In radiated arteries, plaque area was significantly larger (32% larger then in sham). Macrophage-positive area in radiated arteries was 2.4 times greater than the macrophage-positive area in the nonradiated arteries. The area positive for macrophages is also positive for metalloproteinases (MMP)-1. The extent of α-actin positive area was significantly less (2.3-fold) in radiated arteries. The atherosclerotic plaque developed in the current model is predominantly composed of macrophages expressing metalloproteinases with few smooth muscle cells (SMC)—a characteristic of vulnerable plaque. The animal model presented in this study can elucidate at least part of the mechanism of plaque vulnerability and could be used to test treatment modalities to test plaque stability.
doi_str_mv 10.1016/S1522-1865(03)00182-3
format Article
fullrecord <record><control><sourceid>elsevier_pubme</sourceid><recordid>TN_cdi_pubmed_primary_14984715</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S1522186503001823</els_id><sourcerecordid>S1522186503001823</sourcerecordid><originalsourceid>FETCH-LOGICAL-e180t-de56cef911d3e54a81cc1f07b6c237c162bf7477a2a3f8d2223cfba9fc9a48383</originalsourceid><addsrcrecordid>eNo9kE1PAjEQhnvQCKI_QbNHPaz2Yz-6XgghKiQaCX5cm247KzVlF9tdEg7-dwuIl5lk5smbmQehC4JvCCbZ7StJKY0Jz9IrzK4xJpzG7Aj1_8c9dOr9V1hkBctPUI8kBU9ykvbRz1xqI1vT1PG01p0CHY3aBbjGKxtqa1Q0s_K7g2jmmk8H3gc0MnUko8lmBU4tGgu-DaiFZYDnsixNexeNtrxfgWrNGqKPztbgZGnhkPbcaLDDM3RcSevh_K8P0PvD_dt4Ej-9PE7Ho6cYCMdtrCHNFFQFIZpBmkhOlCIVzstMUZYrktGyypM8l1SyimtKKVNVKYtKFTLhjLMButznrrpyCVqsnFlKtxEHDwEY7gEIV6wNOOGVgTroMC78IHRjBMFia1vsbIutVoGZ2NkWjP0CRDh1jg</addsrcrecordid><sourcetype>Index Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Radiation-Induced Atherosclerotic Plaque Progression in a Hypercholesterolemic Rabbit: A Prospective Vulnerable Plaque Model?</title><source>MEDLINE</source><source>Alma/SFX Local Collection</source><creator>Pakala, Rajbabu ; Leborgne, Laurent ; Cheneau, Edouard ; Chan, Rosanna C. ; Yazdi, Hamid ; Fournadjiev, Jana ; Weber, Deena ; Hellinga, David ; Kolodgie, Frank ; Virmani, Renu ; Waksman, Ron</creator><creatorcontrib>Pakala, Rajbabu ; Leborgne, Laurent ; Cheneau, Edouard ; Chan, Rosanna C. ; Yazdi, Hamid ; Fournadjiev, Jana ; Weber, Deena ; Hellinga, David ; Kolodgie, Frank ; Virmani, Renu ; Waksman, Ron</creatorcontrib><description>Human observations provide rich soil for making hypotheses, but good animal models are essential for understanding the disease and to test treatment modalities. Currently, there is no standard animal model of vulnerable plaque; therefore, the purpose of this study is to develop a pathophysiologically relevant vulnerable plaque model. New Zealand White rabbits were fed with 1% hypercholesterolemic (HC) diet for 7 days, followed by balloon denudation of both the iliac arteries, and continued on 1% HC diet. Four weeks later, in 12 rabbits one of the iliac arteries was radiated (192-Ir, 15 Gy), and in five rabbits both the iliac arteries were sham treated. Following that, rabbits were fed with 0.15% HC diet. Four weeks later, arteries were processed for histomorphometry or immunohistochemistry. Serum cholesterol levels were similar in all the groups. In radiated arteries, plaque area was significantly larger (32% larger then in sham). Macrophage-positive area in radiated arteries was 2.4 times greater than the macrophage-positive area in the nonradiated arteries. The area positive for macrophages is also positive for metalloproteinases (MMP)-1. The extent of α-actin positive area was significantly less (2.3-fold) in radiated arteries. The atherosclerotic plaque developed in the current model is predominantly composed of macrophages expressing metalloproteinases with few smooth muscle cells (SMC)—a characteristic of vulnerable plaque. The animal model presented in this study can elucidate at least part of the mechanism of plaque vulnerability and could be used to test treatment modalities to test plaque stability.</description><identifier>ISSN: 1522-1865</identifier><identifier>DOI: 10.1016/S1522-1865(03)00182-3</identifier><identifier>PMID: 14984715</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Animals ; Arteries - metabolism ; Arteries - pathology ; Arteries - radiation effects ; Arteriosclerosis - etiology ; Arteriosclerosis - metabolism ; Arteriosclerosis - pathology ; Atherosclerosis ; Disease Models, Animal ; Disease Progression ; Hypercholesterolemia - metabolism ; Hypercholesterolemia - pathology ; Immunohistochemistry ; Lipids - blood ; Macrophages ; Macrophages - metabolism ; Macrophages - pathology ; Macrophages - radiation effects ; Male ; Matrix Metalloproteinase 1 - metabolism ; Metalloproteinases ; Models, Cardiovascular ; Myocytes, Smooth Muscle - metabolism ; Myocytes, Smooth Muscle - pathology ; Myocytes, Smooth Muscle - radiation effects ; Prospective Studies ; Rabbits ; Radiation ; Radiation Injuries, Experimental - etiology ; Radiation Injuries, Experimental - metabolism ; Radiation Injuries, Experimental - pathology ; Smooth muscle cells ; Tunica Intima - metabolism ; Tunica Intima - pathology ; Tunica Intima - radiation effects ; Vulnerable plaque</subject><ispartof>Cardiovascular radiation medicine, 2003-07, Vol.4 (3), p.146-151</ispartof><rights>2004 Elsevier Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,27905,27906</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/14984715$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Pakala, Rajbabu</creatorcontrib><creatorcontrib>Leborgne, Laurent</creatorcontrib><creatorcontrib>Cheneau, Edouard</creatorcontrib><creatorcontrib>Chan, Rosanna C.</creatorcontrib><creatorcontrib>Yazdi, Hamid</creatorcontrib><creatorcontrib>Fournadjiev, Jana</creatorcontrib><creatorcontrib>Weber, Deena</creatorcontrib><creatorcontrib>Hellinga, David</creatorcontrib><creatorcontrib>Kolodgie, Frank</creatorcontrib><creatorcontrib>Virmani, Renu</creatorcontrib><creatorcontrib>Waksman, Ron</creatorcontrib><title>Radiation-Induced Atherosclerotic Plaque Progression in a Hypercholesterolemic Rabbit: A Prospective Vulnerable Plaque Model?</title><title>Cardiovascular radiation medicine</title><addtitle>Cardiovasc Radiat Med</addtitle><description>Human observations provide rich soil for making hypotheses, but good animal models are essential for understanding the disease and to test treatment modalities. Currently, there is no standard animal model of vulnerable plaque; therefore, the purpose of this study is to develop a pathophysiologically relevant vulnerable plaque model. New Zealand White rabbits were fed with 1% hypercholesterolemic (HC) diet for 7 days, followed by balloon denudation of both the iliac arteries, and continued on 1% HC diet. Four weeks later, in 12 rabbits one of the iliac arteries was radiated (192-Ir, 15 Gy), and in five rabbits both the iliac arteries were sham treated. Following that, rabbits were fed with 0.15% HC diet. Four weeks later, arteries were processed for histomorphometry or immunohistochemistry. Serum cholesterol levels were similar in all the groups. In radiated arteries, plaque area was significantly larger (32% larger then in sham). Macrophage-positive area in radiated arteries was 2.4 times greater than the macrophage-positive area in the nonradiated arteries. The area positive for macrophages is also positive for metalloproteinases (MMP)-1. The extent of α-actin positive area was significantly less (2.3-fold) in radiated arteries. The atherosclerotic plaque developed in the current model is predominantly composed of macrophages expressing metalloproteinases with few smooth muscle cells (SMC)—a characteristic of vulnerable plaque. The animal model presented in this study can elucidate at least part of the mechanism of plaque vulnerability and could be used to test treatment modalities to test plaque stability.</description><subject>Animals</subject><subject>Arteries - metabolism</subject><subject>Arteries - pathology</subject><subject>Arteries - radiation effects</subject><subject>Arteriosclerosis - etiology</subject><subject>Arteriosclerosis - metabolism</subject><subject>Arteriosclerosis - pathology</subject><subject>Atherosclerosis</subject><subject>Disease Models, Animal</subject><subject>Disease Progression</subject><subject>Hypercholesterolemia - metabolism</subject><subject>Hypercholesterolemia - pathology</subject><subject>Immunohistochemistry</subject><subject>Lipids - blood</subject><subject>Macrophages</subject><subject>Macrophages - metabolism</subject><subject>Macrophages - pathology</subject><subject>Macrophages - radiation effects</subject><subject>Male</subject><subject>Matrix Metalloproteinase 1 - metabolism</subject><subject>Metalloproteinases</subject><subject>Models, Cardiovascular</subject><subject>Myocytes, Smooth Muscle - metabolism</subject><subject>Myocytes, Smooth Muscle - pathology</subject><subject>Myocytes, Smooth Muscle - radiation effects</subject><subject>Prospective Studies</subject><subject>Rabbits</subject><subject>Radiation</subject><subject>Radiation Injuries, Experimental - etiology</subject><subject>Radiation Injuries, Experimental - metabolism</subject><subject>Radiation Injuries, Experimental - pathology</subject><subject>Smooth muscle cells</subject><subject>Tunica Intima - metabolism</subject><subject>Tunica Intima - pathology</subject><subject>Tunica Intima - radiation effects</subject><subject>Vulnerable plaque</subject><issn>1522-1865</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo9kE1PAjEQhnvQCKI_QbNHPaz2Yz-6XgghKiQaCX5cm247KzVlF9tdEg7-dwuIl5lk5smbmQehC4JvCCbZ7StJKY0Jz9IrzK4xJpzG7Aj1_8c9dOr9V1hkBctPUI8kBU9ykvbRz1xqI1vT1PG01p0CHY3aBbjGKxtqa1Q0s_K7g2jmmk8H3gc0MnUko8lmBU4tGgu-DaiFZYDnsixNexeNtrxfgWrNGqKPztbgZGnhkPbcaLDDM3RcSevh_K8P0PvD_dt4Ej-9PE7Ho6cYCMdtrCHNFFQFIZpBmkhOlCIVzstMUZYrktGyypM8l1SyimtKKVNVKYtKFTLhjLMButznrrpyCVqsnFlKtxEHDwEY7gEIV6wNOOGVgTroMC78IHRjBMFia1vsbIutVoGZ2NkWjP0CRDh1jg</recordid><startdate>200307</startdate><enddate>200307</enddate><creator>Pakala, Rajbabu</creator><creator>Leborgne, Laurent</creator><creator>Cheneau, Edouard</creator><creator>Chan, Rosanna C.</creator><creator>Yazdi, Hamid</creator><creator>Fournadjiev, Jana</creator><creator>Weber, Deena</creator><creator>Hellinga, David</creator><creator>Kolodgie, Frank</creator><creator>Virmani, Renu</creator><creator>Waksman, Ron</creator><general>Elsevier Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope></search><sort><creationdate>200307</creationdate><title>Radiation-Induced Atherosclerotic Plaque Progression in a Hypercholesterolemic Rabbit: A Prospective Vulnerable Plaque Model?</title><author>Pakala, Rajbabu ; Leborgne, Laurent ; Cheneau, Edouard ; Chan, Rosanna C. ; Yazdi, Hamid ; Fournadjiev, Jana ; Weber, Deena ; Hellinga, David ; Kolodgie, Frank ; Virmani, Renu ; Waksman, Ron</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-e180t-de56cef911d3e54a81cc1f07b6c237c162bf7477a2a3f8d2223cfba9fc9a48383</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>Animals</topic><topic>Arteries - metabolism</topic><topic>Arteries - pathology</topic><topic>Arteries - radiation effects</topic><topic>Arteriosclerosis - etiology</topic><topic>Arteriosclerosis - metabolism</topic><topic>Arteriosclerosis - pathology</topic><topic>Atherosclerosis</topic><topic>Disease Models, Animal</topic><topic>Disease Progression</topic><topic>Hypercholesterolemia - metabolism</topic><topic>Hypercholesterolemia - pathology</topic><topic>Immunohistochemistry</topic><topic>Lipids - blood</topic><topic>Macrophages</topic><topic>Macrophages - metabolism</topic><topic>Macrophages - pathology</topic><topic>Macrophages - radiation effects</topic><topic>Male</topic><topic>Matrix Metalloproteinase 1 - metabolism</topic><topic>Metalloproteinases</topic><topic>Models, Cardiovascular</topic><topic>Myocytes, Smooth Muscle - metabolism</topic><topic>Myocytes, Smooth Muscle - pathology</topic><topic>Myocytes, Smooth Muscle - radiation effects</topic><topic>Prospective Studies</topic><topic>Rabbits</topic><topic>Radiation</topic><topic>Radiation Injuries, Experimental - etiology</topic><topic>Radiation Injuries, Experimental - metabolism</topic><topic>Radiation Injuries, Experimental - pathology</topic><topic>Smooth muscle cells</topic><topic>Tunica Intima - metabolism</topic><topic>Tunica Intima - pathology</topic><topic>Tunica Intima - radiation effects</topic><topic>Vulnerable plaque</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Pakala, Rajbabu</creatorcontrib><creatorcontrib>Leborgne, Laurent</creatorcontrib><creatorcontrib>Cheneau, Edouard</creatorcontrib><creatorcontrib>Chan, Rosanna C.</creatorcontrib><creatorcontrib>Yazdi, Hamid</creatorcontrib><creatorcontrib>Fournadjiev, Jana</creatorcontrib><creatorcontrib>Weber, Deena</creatorcontrib><creatorcontrib>Hellinga, David</creatorcontrib><creatorcontrib>Kolodgie, Frank</creatorcontrib><creatorcontrib>Virmani, Renu</creatorcontrib><creatorcontrib>Waksman, Ron</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><jtitle>Cardiovascular radiation medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Pakala, Rajbabu</au><au>Leborgne, Laurent</au><au>Cheneau, Edouard</au><au>Chan, Rosanna C.</au><au>Yazdi, Hamid</au><au>Fournadjiev, Jana</au><au>Weber, Deena</au><au>Hellinga, David</au><au>Kolodgie, Frank</au><au>Virmani, Renu</au><au>Waksman, Ron</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Radiation-Induced Atherosclerotic Plaque Progression in a Hypercholesterolemic Rabbit: A Prospective Vulnerable Plaque Model?</atitle><jtitle>Cardiovascular radiation medicine</jtitle><addtitle>Cardiovasc Radiat Med</addtitle><date>2003-07</date><risdate>2003</risdate><volume>4</volume><issue>3</issue><spage>146</spage><epage>151</epage><pages>146-151</pages><issn>1522-1865</issn><abstract>Human observations provide rich soil for making hypotheses, but good animal models are essential for understanding the disease and to test treatment modalities. Currently, there is no standard animal model of vulnerable plaque; therefore, the purpose of this study is to develop a pathophysiologically relevant vulnerable plaque model. New Zealand White rabbits were fed with 1% hypercholesterolemic (HC) diet for 7 days, followed by balloon denudation of both the iliac arteries, and continued on 1% HC diet. Four weeks later, in 12 rabbits one of the iliac arteries was radiated (192-Ir, 15 Gy), and in five rabbits both the iliac arteries were sham treated. Following that, rabbits were fed with 0.15% HC diet. Four weeks later, arteries were processed for histomorphometry or immunohistochemistry. Serum cholesterol levels were similar in all the groups. In radiated arteries, plaque area was significantly larger (32% larger then in sham). Macrophage-positive area in radiated arteries was 2.4 times greater than the macrophage-positive area in the nonradiated arteries. The area positive for macrophages is also positive for metalloproteinases (MMP)-1. The extent of α-actin positive area was significantly less (2.3-fold) in radiated arteries. The atherosclerotic plaque developed in the current model is predominantly composed of macrophages expressing metalloproteinases with few smooth muscle cells (SMC)—a characteristic of vulnerable plaque. The animal model presented in this study can elucidate at least part of the mechanism of plaque vulnerability and could be used to test treatment modalities to test plaque stability.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>14984715</pmid><doi>10.1016/S1522-1865(03)00182-3</doi><tpages>6</tpages></addata></record>
fulltext fulltext
identifier ISSN: 1522-1865
ispartof Cardiovascular radiation medicine, 2003-07, Vol.4 (3), p.146-151
issn 1522-1865
language eng
recordid cdi_pubmed_primary_14984715
source MEDLINE; Alma/SFX Local Collection
subjects Animals
Arteries - metabolism
Arteries - pathology
Arteries - radiation effects
Arteriosclerosis - etiology
Arteriosclerosis - metabolism
Arteriosclerosis - pathology
Atherosclerosis
Disease Models, Animal
Disease Progression
Hypercholesterolemia - metabolism
Hypercholesterolemia - pathology
Immunohistochemistry
Lipids - blood
Macrophages
Macrophages - metabolism
Macrophages - pathology
Macrophages - radiation effects
Male
Matrix Metalloproteinase 1 - metabolism
Metalloproteinases
Models, Cardiovascular
Myocytes, Smooth Muscle - metabolism
Myocytes, Smooth Muscle - pathology
Myocytes, Smooth Muscle - radiation effects
Prospective Studies
Rabbits
Radiation
Radiation Injuries, Experimental - etiology
Radiation Injuries, Experimental - metabolism
Radiation Injuries, Experimental - pathology
Smooth muscle cells
Tunica Intima - metabolism
Tunica Intima - pathology
Tunica Intima - radiation effects
Vulnerable plaque
title Radiation-Induced Atherosclerotic Plaque Progression in a Hypercholesterolemic Rabbit: A Prospective Vulnerable Plaque Model?
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-17T21%3A13%3A49IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-elsevier_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Radiation-Induced%20Atherosclerotic%20Plaque%20Progression%20in%20a%20Hypercholesterolemic%20Rabbit:%20A%20Prospective%20Vulnerable%20Plaque%20Model?&rft.jtitle=Cardiovascular%20radiation%20medicine&rft.au=Pakala,%20Rajbabu&rft.date=2003-07&rft.volume=4&rft.issue=3&rft.spage=146&rft.epage=151&rft.pages=146-151&rft.issn=1522-1865&rft_id=info:doi/10.1016/S1522-1865(03)00182-3&rft_dat=%3Celsevier_pubme%3ES1522186503001823%3C/elsevier_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/14984715&rft_els_id=S1522186503001823&rfr_iscdi=true