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HDL mimetic peptide CER-522 treatment regresses left ventricular diastolic dysfunction in cholesterol-fed rabbits
Abstract Objectives High-density lipoprotein (HDL) infusions induce rapid improvement of experimental atherosclerosis in rabbits but their effect on ventricular function remains unknown. We aimed to evaluate the effects of the HDL mimetic peptide CER522 on left ventricular diastolic dysfunction (LV...
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Published in: | International journal of cardiology 2016-07, Vol.215, p.364-371 |
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creator | Merlet, Nolwenn Busseuil, David Mihalache-Avram, Teodora Mecteau, Melanie Shi, Yanfen Nachar, Walid Brand, Genevieve Brodeur, Mathieu R Charpentier, Daniel Rhainds, David Sy, Gavin Schwendeman, Anna Lalwani, Narendra Dasseux, Jean-Louis Rhéaume, Eric Tardif, Jean-Claude |
description | Abstract Objectives High-density lipoprotein (HDL) infusions induce rapid improvement of experimental atherosclerosis in rabbits but their effect on ventricular function remains unknown. We aimed to evaluate the effects of the HDL mimetic peptide CER522 on left ventricular diastolic dysfunction (LVDD). Methods Rabbits were fed with a cholesterol- and vitamin D2 -enriched diet until mild aortic valve stenosis and hypercholesterolemia-induced LV hypertrophy and LVDD developed. Animals then received saline or 10 or 30 mg/kg CER522 infusions 6 times over 2 weeks. We performed serial echocardiograms and LV histology to evaluate the effects of CER522 therapy on LVDD. Results LVDD was reduced by CER-522 as shown by multiple parameters including early filling mitral deceleration time, deceleration rate, Em/Am ratio, E/Em ratio, pulmonary venous velocities, and LVDD score. These findings were associated with reduced macrophages (RAM-11 positive cells) in the pericoronary area and LV, and decreased levels of apoptotic cardiomyocytes in CER522-treated rabbits. CER-522 treatment also resulted in decreased atheromatous plaques and internal elastic lamina area in coronary arteries. Conclusions CER522 improves LVDD in rabbits, with reductions of LV macrophage accumulation, cardiomyocyte apoptosis, coronary atherosclerosis and remodelling. |
doi_str_mv | 10.1016/j.ijcard.2016.04.029 |
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We aimed to evaluate the effects of the HDL mimetic peptide CER522 on left ventricular diastolic dysfunction (LVDD). Methods Rabbits were fed with a cholesterol- and vitamin D2 -enriched diet until mild aortic valve stenosis and hypercholesterolemia-induced LV hypertrophy and LVDD developed. Animals then received saline or 10 or 30 mg/kg CER522 infusions 6 times over 2 weeks. We performed serial echocardiograms and LV histology to evaluate the effects of CER522 therapy on LVDD. Results LVDD was reduced by CER-522 as shown by multiple parameters including early filling mitral deceleration time, deceleration rate, Em/Am ratio, E/Em ratio, pulmonary venous velocities, and LVDD score. These findings were associated with reduced macrophages (RAM-11 positive cells) in the pericoronary area and LV, and decreased levels of apoptotic cardiomyocytes in CER522-treated rabbits. CER-522 treatment also resulted in decreased atheromatous plaques and internal elastic lamina area in coronary arteries. Conclusions CER522 improves LVDD in rabbits, with reductions of LV macrophage accumulation, cardiomyocyte apoptosis, coronary atherosclerosis and remodelling.</description><identifier>ISSN: 0167-5273</identifier><identifier>EISSN: 1874-1754</identifier><identifier>DOI: 10.1016/j.ijcard.2016.04.029</identifier><identifier>PMID: 27128563</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Animals ; Aortic Valve Stenosis - chemically induced ; Aortic Valve Stenosis - physiopathology ; Apoptosis - drug effects ; Cardiovascular ; Cells, Cultured ; Cholesterol - administration & dosage ; Cholesterol - adverse effects ; Disease Models, Animal ; Echocardiography-Doppler ; High-density lipoprotein ; Humans ; Hypercholesterolemia - chemically induced ; Hypercholesterolemia - physiopathology ; Hypertrophy, Left Ventricular - drug therapy ; Hypertrophy, Left Ventricular - physiopathology ; Inflammation ; Left ventricular diastolic dysfunction ; Lipoproteins, HDL - chemistry ; Macrophages - cytology ; Macrophages - drug effects ; Myocytes, Cardiac - cytology ; Myocytes, Cardiac - drug effects ; Peptidomimetics - administration & dosage ; Peptidomimetics - pharmacology ; Rabbits ; Ventricular Dysfunction, Left - drug therapy ; Ventricular Dysfunction, Left - physiopathology</subject><ispartof>International journal of cardiology, 2016-07, Vol.215, p.364-371</ispartof><rights>2016 Elsevier Ireland Ltd</rights><rights>Copyright © 2016 Elsevier Ireland Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c450t-38d809f8a65ec35fdc0623f98529bc6da1b27018a6e296e4a8333b69f73475693</citedby><cites>FETCH-LOGICAL-c450t-38d809f8a65ec35fdc0623f98529bc6da1b27018a6e296e4a8333b69f73475693</cites><orcidid>0000-0003-1198-9953 ; 0000-0002-0092-2326</orcidid></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/27128563$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Merlet, Nolwenn</creatorcontrib><creatorcontrib>Busseuil, David</creatorcontrib><creatorcontrib>Mihalache-Avram, Teodora</creatorcontrib><creatorcontrib>Mecteau, Melanie</creatorcontrib><creatorcontrib>Shi, Yanfen</creatorcontrib><creatorcontrib>Nachar, Walid</creatorcontrib><creatorcontrib>Brand, Genevieve</creatorcontrib><creatorcontrib>Brodeur, Mathieu R</creatorcontrib><creatorcontrib>Charpentier, Daniel</creatorcontrib><creatorcontrib>Rhainds, David</creatorcontrib><creatorcontrib>Sy, Gavin</creatorcontrib><creatorcontrib>Schwendeman, Anna</creatorcontrib><creatorcontrib>Lalwani, Narendra</creatorcontrib><creatorcontrib>Dasseux, Jean-Louis</creatorcontrib><creatorcontrib>Rhéaume, Eric</creatorcontrib><creatorcontrib>Tardif, Jean-Claude</creatorcontrib><title>HDL mimetic peptide CER-522 treatment regresses left ventricular diastolic dysfunction in cholesterol-fed rabbits</title><title>International journal of cardiology</title><addtitle>Int J Cardiol</addtitle><description>Abstract Objectives High-density lipoprotein (HDL) infusions induce rapid improvement of experimental atherosclerosis in rabbits but their effect on ventricular function remains unknown. We aimed to evaluate the effects of the HDL mimetic peptide CER522 on left ventricular diastolic dysfunction (LVDD). Methods Rabbits were fed with a cholesterol- and vitamin D2 -enriched diet until mild aortic valve stenosis and hypercholesterolemia-induced LV hypertrophy and LVDD developed. Animals then received saline or 10 or 30 mg/kg CER522 infusions 6 times over 2 weeks. We performed serial echocardiograms and LV histology to evaluate the effects of CER522 therapy on LVDD. Results LVDD was reduced by CER-522 as shown by multiple parameters including early filling mitral deceleration time, deceleration rate, Em/Am ratio, E/Em ratio, pulmonary venous velocities, and LVDD score. These findings were associated with reduced macrophages (RAM-11 positive cells) in the pericoronary area and LV, and decreased levels of apoptotic cardiomyocytes in CER522-treated rabbits. CER-522 treatment also resulted in decreased atheromatous plaques and internal elastic lamina area in coronary arteries. Conclusions CER522 improves LVDD in rabbits, with reductions of LV macrophage accumulation, cardiomyocyte apoptosis, coronary atherosclerosis and remodelling.</description><subject>Animals</subject><subject>Aortic Valve Stenosis - chemically induced</subject><subject>Aortic Valve Stenosis - physiopathology</subject><subject>Apoptosis - drug effects</subject><subject>Cardiovascular</subject><subject>Cells, Cultured</subject><subject>Cholesterol - administration & dosage</subject><subject>Cholesterol - adverse effects</subject><subject>Disease Models, Animal</subject><subject>Echocardiography-Doppler</subject><subject>High-density lipoprotein</subject><subject>Humans</subject><subject>Hypercholesterolemia - chemically induced</subject><subject>Hypercholesterolemia - physiopathology</subject><subject>Hypertrophy, Left Ventricular - drug therapy</subject><subject>Hypertrophy, Left Ventricular - physiopathology</subject><subject>Inflammation</subject><subject>Left ventricular diastolic dysfunction</subject><subject>Lipoproteins, HDL - chemistry</subject><subject>Macrophages - cytology</subject><subject>Macrophages - drug effects</subject><subject>Myocytes, Cardiac - cytology</subject><subject>Myocytes, Cardiac - drug effects</subject><subject>Peptidomimetics - administration & dosage</subject><subject>Peptidomimetics - pharmacology</subject><subject>Rabbits</subject><subject>Ventricular Dysfunction, Left - drug therapy</subject><subject>Ventricular Dysfunction, Left - physiopathology</subject><issn>0167-5273</issn><issn>1874-1754</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><recordid>eNqFkk1v1DAQhi0EotvCP0DIRy4J_oodX5DQtlCklZD4OFuOPQEvTrK1nUr77_FqWw5cehp55n1nrHkGoTeUtJRQ-X7fhr2zybesvloiWsL0M7ShvRINVZ14jja1oJqOKX6BLnPeE0KE1v1LdMEUZX0n-Qbd3V7v8BQmKMHhAxxK8IC3N9-qjeGSwJYJ5oIT_EqQM2QcYSz4vuZScGu0Cftgc1litftjHtfZlbDMOMzY_V4i5AJpic0IHic7DKHkV-jFaGOG1w_xCv38dPNje9vsvn7-sv24a5zoSGl473uix97KDhzvRu-IZHzUfcf04KS3dGCK0FoHpiUI23POB6lHxYXqpOZX6N257yEtd2v9iJlCdhCjnWFZs6E9pZoISeTTUqUpZ7yjvErFWerSknOC0RxSmGw6GkrMiYvZmzMXc-JiiDCVS7W9fZiwDhP4f6ZHEFXw4SyAupL7AMlkF2B24EMCV4xfwlMT_m_gYpiDs_EPHCHvlzXNdd2GmswMMd9Pt3E6DSo5UZRL_hfEvrT4</recordid><startdate>20160715</startdate><enddate>20160715</enddate><creator>Merlet, Nolwenn</creator><creator>Busseuil, David</creator><creator>Mihalache-Avram, Teodora</creator><creator>Mecteau, Melanie</creator><creator>Shi, Yanfen</creator><creator>Nachar, Walid</creator><creator>Brand, Genevieve</creator><creator>Brodeur, Mathieu R</creator><creator>Charpentier, Daniel</creator><creator>Rhainds, David</creator><creator>Sy, Gavin</creator><creator>Schwendeman, Anna</creator><creator>Lalwani, Narendra</creator><creator>Dasseux, Jean-Louis</creator><creator>Rhéaume, Eric</creator><creator>Tardif, Jean-Claude</creator><general>Elsevier B.V</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><scope>7TS</scope><orcidid>https://orcid.org/0000-0003-1198-9953</orcidid><orcidid>https://orcid.org/0000-0002-0092-2326</orcidid></search><sort><creationdate>20160715</creationdate><title>HDL mimetic peptide CER-522 treatment regresses left ventricular diastolic dysfunction in cholesterol-fed rabbits</title><author>Merlet, Nolwenn ; Busseuil, David ; Mihalache-Avram, Teodora ; Mecteau, Melanie ; Shi, Yanfen ; Nachar, Walid ; Brand, Genevieve ; Brodeur, Mathieu R ; Charpentier, Daniel ; Rhainds, David ; Sy, Gavin ; Schwendeman, Anna ; Lalwani, Narendra ; Dasseux, Jean-Louis ; Rhéaume, Eric ; Tardif, Jean-Claude</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c450t-38d809f8a65ec35fdc0623f98529bc6da1b27018a6e296e4a8333b69f73475693</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Animals</topic><topic>Aortic Valve Stenosis - chemically induced</topic><topic>Aortic Valve Stenosis - physiopathology</topic><topic>Apoptosis - drug effects</topic><topic>Cardiovascular</topic><topic>Cells, Cultured</topic><topic>Cholesterol - administration & dosage</topic><topic>Cholesterol - adverse effects</topic><topic>Disease Models, Animal</topic><topic>Echocardiography-Doppler</topic><topic>High-density lipoprotein</topic><topic>Humans</topic><topic>Hypercholesterolemia - chemically induced</topic><topic>Hypercholesterolemia - physiopathology</topic><topic>Hypertrophy, Left Ventricular - drug therapy</topic><topic>Hypertrophy, Left Ventricular - physiopathology</topic><topic>Inflammation</topic><topic>Left ventricular diastolic dysfunction</topic><topic>Lipoproteins, HDL - chemistry</topic><topic>Macrophages - cytology</topic><topic>Macrophages - drug effects</topic><topic>Myocytes, Cardiac - cytology</topic><topic>Myocytes, Cardiac - drug effects</topic><topic>Peptidomimetics - administration & dosage</topic><topic>Peptidomimetics - pharmacology</topic><topic>Rabbits</topic><topic>Ventricular Dysfunction, Left - drug therapy</topic><topic>Ventricular Dysfunction, Left - physiopathology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Merlet, Nolwenn</creatorcontrib><creatorcontrib>Busseuil, David</creatorcontrib><creatorcontrib>Mihalache-Avram, Teodora</creatorcontrib><creatorcontrib>Mecteau, Melanie</creatorcontrib><creatorcontrib>Shi, Yanfen</creatorcontrib><creatorcontrib>Nachar, Walid</creatorcontrib><creatorcontrib>Brand, Genevieve</creatorcontrib><creatorcontrib>Brodeur, Mathieu R</creatorcontrib><creatorcontrib>Charpentier, Daniel</creatorcontrib><creatorcontrib>Rhainds, David</creatorcontrib><creatorcontrib>Sy, Gavin</creatorcontrib><creatorcontrib>Schwendeman, Anna</creatorcontrib><creatorcontrib>Lalwani, Narendra</creatorcontrib><creatorcontrib>Dasseux, Jean-Louis</creatorcontrib><creatorcontrib>Rhéaume, Eric</creatorcontrib><creatorcontrib>Tardif, Jean-Claude</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><collection>Physical Education Index</collection><jtitle>International journal of cardiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Merlet, Nolwenn</au><au>Busseuil, David</au><au>Mihalache-Avram, Teodora</au><au>Mecteau, Melanie</au><au>Shi, Yanfen</au><au>Nachar, Walid</au><au>Brand, Genevieve</au><au>Brodeur, Mathieu R</au><au>Charpentier, Daniel</au><au>Rhainds, David</au><au>Sy, Gavin</au><au>Schwendeman, Anna</au><au>Lalwani, Narendra</au><au>Dasseux, Jean-Louis</au><au>Rhéaume, Eric</au><au>Tardif, Jean-Claude</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>HDL mimetic peptide CER-522 treatment regresses left ventricular diastolic dysfunction in cholesterol-fed rabbits</atitle><jtitle>International journal of cardiology</jtitle><addtitle>Int J Cardiol</addtitle><date>2016-07-15</date><risdate>2016</risdate><volume>215</volume><spage>364</spage><epage>371</epage><pages>364-371</pages><issn>0167-5273</issn><eissn>1874-1754</eissn><abstract>Abstract Objectives High-density lipoprotein (HDL) infusions induce rapid improvement of experimental atherosclerosis in rabbits but their effect on ventricular function remains unknown. We aimed to evaluate the effects of the HDL mimetic peptide CER522 on left ventricular diastolic dysfunction (LVDD). Methods Rabbits were fed with a cholesterol- and vitamin D2 -enriched diet until mild aortic valve stenosis and hypercholesterolemia-induced LV hypertrophy and LVDD developed. Animals then received saline or 10 or 30 mg/kg CER522 infusions 6 times over 2 weeks. We performed serial echocardiograms and LV histology to evaluate the effects of CER522 therapy on LVDD. Results LVDD was reduced by CER-522 as shown by multiple parameters including early filling mitral deceleration time, deceleration rate, Em/Am ratio, E/Em ratio, pulmonary venous velocities, and LVDD score. These findings were associated with reduced macrophages (RAM-11 positive cells) in the pericoronary area and LV, and decreased levels of apoptotic cardiomyocytes in CER522-treated rabbits. CER-522 treatment also resulted in decreased atheromatous plaques and internal elastic lamina area in coronary arteries. Conclusions CER522 improves LVDD in rabbits, with reductions of LV macrophage accumulation, cardiomyocyte apoptosis, coronary atherosclerosis and remodelling.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>27128563</pmid><doi>10.1016/j.ijcard.2016.04.029</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0003-1198-9953</orcidid><orcidid>https://orcid.org/0000-0002-0092-2326</orcidid></addata></record> |
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subjects | Animals Aortic Valve Stenosis - chemically induced Aortic Valve Stenosis - physiopathology Apoptosis - drug effects Cardiovascular Cells, Cultured Cholesterol - administration & dosage Cholesterol - adverse effects Disease Models, Animal Echocardiography-Doppler High-density lipoprotein Humans Hypercholesterolemia - chemically induced Hypercholesterolemia - physiopathology Hypertrophy, Left Ventricular - drug therapy Hypertrophy, Left Ventricular - physiopathology Inflammation Left ventricular diastolic dysfunction Lipoproteins, HDL - chemistry Macrophages - cytology Macrophages - drug effects Myocytes, Cardiac - cytology Myocytes, Cardiac - drug effects Peptidomimetics - administration & dosage Peptidomimetics - pharmacology Rabbits Ventricular Dysfunction, Left - drug therapy Ventricular Dysfunction, Left - physiopathology |
title | HDL mimetic peptide CER-522 treatment regresses left ventricular diastolic dysfunction in cholesterol-fed rabbits |
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