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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
Main Authors: 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
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cited_by cdi_FETCH-LOGICAL-c450t-38d809f8a65ec35fdc0623f98529bc6da1b27018a6e296e4a8333b69f73475693
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container_end_page 371
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container_start_page 364
container_title International journal of cardiology
container_volume 215
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 &amp; 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 &amp; 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. 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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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