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Preservation of Post-Infarction Cardiac Structure and Function via Long-Term Oral Formyl Peptide Receptor Agonist Treatment
Dysregulated inflammation following myocardial infarction (MI) promotes left ventricular (LV) remodeling and loss of function. Targeting inflammation resolution by activating formyl peptide receptors (FPRs) may limit adverse remodeling and progression towards heart failure. This study characterized...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6939031/ https://www.ncbi.nlm.nih.gov/pubmed/31909300 http://dx.doi.org/10.1016/j.jacbts.2019.07.005 |
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author | García, Ricardo A. Ito, Bruce R. Lupisella, John A. Carson, Nancy A. Hsu, Mei-Yin Fernando, Gayani Heroux, Madeleine Bouvier, Michel Dierks, Elizabeth Kick, Ellen K. Gordon, David A. Chen, Jian Mintier, Gabe Carrier, Marilyn St-Onge, Stéphane Shah, Himanshu Towne, Jordan Bucardo, Marcela Sotelo Ma, Xiuying Ryan, Carol S. Wurtz, Nicholas R. Ostrowski, Jacek Villarreal, Francisco J. |
author_facet | García, Ricardo A. Ito, Bruce R. Lupisella, John A. Carson, Nancy A. Hsu, Mei-Yin Fernando, Gayani Heroux, Madeleine Bouvier, Michel Dierks, Elizabeth Kick, Ellen K. Gordon, David A. Chen, Jian Mintier, Gabe Carrier, Marilyn St-Onge, Stéphane Shah, Himanshu Towne, Jordan Bucardo, Marcela Sotelo Ma, Xiuying Ryan, Carol S. Wurtz, Nicholas R. Ostrowski, Jacek Villarreal, Francisco J. |
author_sort | García, Ricardo A. |
collection | PubMed |
description | Dysregulated inflammation following myocardial infarction (MI) promotes left ventricular (LV) remodeling and loss of function. Targeting inflammation resolution by activating formyl peptide receptors (FPRs) may limit adverse remodeling and progression towards heart failure. This study characterized the cellular and signaling properties of Compound 43 (Cmpd43), a dual FPR1/FPR2 agonist, and examined whether Cmpd43 treatment improves LV and infarct remodeling in rodent MI models. Cmpd43 stimulated FPR1/2-mediated signaling, enhanced proresolution cellular function, and modulated cytokines. Cmpd43 increased LV function and reduced chamber remodeling while increasing proresolution macrophage markers. The findings demonstrate that FPR agonism improves cardiac structure and function post-MI. |
format | Online Article Text |
id | pubmed-6939031 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-69390312020-01-06 Preservation of Post-Infarction Cardiac Structure and Function via Long-Term Oral Formyl Peptide Receptor Agonist Treatment García, Ricardo A. Ito, Bruce R. Lupisella, John A. Carson, Nancy A. Hsu, Mei-Yin Fernando, Gayani Heroux, Madeleine Bouvier, Michel Dierks, Elizabeth Kick, Ellen K. Gordon, David A. Chen, Jian Mintier, Gabe Carrier, Marilyn St-Onge, Stéphane Shah, Himanshu Towne, Jordan Bucardo, Marcela Sotelo Ma, Xiuying Ryan, Carol S. Wurtz, Nicholas R. Ostrowski, Jacek Villarreal, Francisco J. JACC Basic Transl Sci PRECLINICAL RESEARCH Dysregulated inflammation following myocardial infarction (MI) promotes left ventricular (LV) remodeling and loss of function. Targeting inflammation resolution by activating formyl peptide receptors (FPRs) may limit adverse remodeling and progression towards heart failure. This study characterized the cellular and signaling properties of Compound 43 (Cmpd43), a dual FPR1/FPR2 agonist, and examined whether Cmpd43 treatment improves LV and infarct remodeling in rodent MI models. Cmpd43 stimulated FPR1/2-mediated signaling, enhanced proresolution cellular function, and modulated cytokines. Cmpd43 increased LV function and reduced chamber remodeling while increasing proresolution macrophage markers. The findings demonstrate that FPR agonism improves cardiac structure and function post-MI. Elsevier 2019-11-13 /pmc/articles/PMC6939031/ /pubmed/31909300 http://dx.doi.org/10.1016/j.jacbts.2019.07.005 Text en © 2019 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | PRECLINICAL RESEARCH García, Ricardo A. Ito, Bruce R. Lupisella, John A. Carson, Nancy A. Hsu, Mei-Yin Fernando, Gayani Heroux, Madeleine Bouvier, Michel Dierks, Elizabeth Kick, Ellen K. Gordon, David A. Chen, Jian Mintier, Gabe Carrier, Marilyn St-Onge, Stéphane Shah, Himanshu Towne, Jordan Bucardo, Marcela Sotelo Ma, Xiuying Ryan, Carol S. Wurtz, Nicholas R. Ostrowski, Jacek Villarreal, Francisco J. Preservation of Post-Infarction Cardiac Structure and Function via Long-Term Oral Formyl Peptide Receptor Agonist Treatment |
title | Preservation of Post-Infarction Cardiac Structure and Function via Long-Term Oral Formyl Peptide Receptor Agonist Treatment |
title_full | Preservation of Post-Infarction Cardiac Structure and Function via Long-Term Oral Formyl Peptide Receptor Agonist Treatment |
title_fullStr | Preservation of Post-Infarction Cardiac Structure and Function via Long-Term Oral Formyl Peptide Receptor Agonist Treatment |
title_full_unstemmed | Preservation of Post-Infarction Cardiac Structure and Function via Long-Term Oral Formyl Peptide Receptor Agonist Treatment |
title_short | Preservation of Post-Infarction Cardiac Structure and Function via Long-Term Oral Formyl Peptide Receptor Agonist Treatment |
title_sort | preservation of post-infarction cardiac structure and function via long-term oral formyl peptide receptor agonist treatment |
topic | PRECLINICAL RESEARCH |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6939031/ https://www.ncbi.nlm.nih.gov/pubmed/31909300 http://dx.doi.org/10.1016/j.jacbts.2019.07.005 |
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