@article{fa875980bb7f40ddb755d9bf6caca0f8,
title = "Guidelines for in vivo mouse models of myocardial infarction",
abstract = "Despite significant improvements in reperfusion strategies, acute coronary syndromes all too often culminate in a myocardial infarction (MI). The consequent MI can, in turn, lead to remodeling of the left ventricle (LV), the development of LV dysfunction, and ultimately progression to heart failure (HF). Accordingly, an improved understanding of the underlying mechanisms of MI remodeling and progression to HF is necessary. One common approach to examine MI pathology is with murine models that recapitulate components of the clinical context of acute coronary syndrome and subsequent MI. We evaluated the different approaches used to produce MI in mouse models and identified opportunities to consolidate methods, recognizing that reperfused and nonreperfused MI yield different responses. The overall goal in compiling this consensus statement is to unify best practices regarding mouse MI models to improve interpretation and allow comparative examination across studies and laboratories. These guidelines will help to establish rigor and reproducibility and provide increased potential for clinical translation.",
keywords = "Cardiac, Ischemia-reperfusion, Myocardial infarction, Rigor and reproducibility, Rodent",
author = "Lindsey, {Merry L.} and Brunt, {Keith R.} and Kirk, {Jonathan A.} and Petra Kleinbongard and Calvert, {John W.} and {de Castro Br{\'a}s}, {Lisandra E.} and DeLeon-Pennell, {Kristine Y.} and {Del Re}, {Dominic P.} and Frangogiannis, {Nikolaos G.} and Stefan Frantz and Gumina, {Richard J.} and Halade, {Ganesh V.} and Jones, {Steven P.} and Ritchie, {Rebecca H.} and Spinale, {Francis G.} and Thorp, {Edward B.} and Ripplinger, {Crystal M.} and Zamaneh Kassiri",
note = "Funding Information: This work was funded by National Institutes of Health Grants GM115458 and HL137319 (to M. L. Lindsey); AA027625, HL136737, and HL147570 (to J. A. Kirk); HL076246, HL085440, and HL149407 (to N. G. Frangogiannis); HL111600 (to C. M. Ripplinger); HL122309 (to E. B. Thorp); HL147844, GM127607, and HL078825 (to S. P. Jones); HL132989 and HL144788 (to G. V. Halade); HL145817 (to K. Y. DeLeon-Pennell); HL130972 (to F. G. Spinale); HL127442 (to R. J. Gumina); DK115213 and HL136915 (to J. W. Calvert); and HL152297 (to L. E. C. Br{\'a}s); Biomedical Laboratory Research and Development Service of the Veterans Affairs Office of Research and Development Grants BX000168 (to F. G. Spinale), BX000505 (to M. L. Lindsey), and BX003922 (to K. Y. DeLeon-Pennell); American Heart Association Innovator Project IPA35260039 (KYD-P); United States Department of Defense Grant PR181464 (to N. G. Frangogiannis); Natural Sciences Engineering Research Council Grants RGPIN-05520 and RGPIN-04878 (to K. R. Brunt); Canadian Institutes of Health Research Grants PJT-37522 and PJT-153306 (to Z. Kassiri) and PJT-421341 and PJo-413883 (to K. R. Brunt); Canadian Foundation for Innovation Grant 31708 (to K. R. Brunt); Heart and Stroke Foundation of Canada Grants G-19–0026282 (to Z. Kassiri) and G-16–00014524 (to K. R. Brunt); Heart and Stroke Foundation of New Brunswick (to K. R. Brunt); American Heart Association Grants 18AIREA33960311 (to L. E. C. Br{\'a}s) and TPA2035490150 (to D. P. Del Re.); National Health and Medical Research Council of Australia Grant APP1158013 (to R. H. Ritchie); and New Brunswick Health Research and Innovation Foundations (to K. R. Brunt). Publisher Copyright: {\textcopyright} 2021 American Physiological Society. All rights reserved.",
year = "2021",
month = dec,
doi = "10.1152/AJPHEART.00459.2021",
language = "English (US)",
volume = "321",
pages = "H1056--H1073",
journal = "American Journal of Physiology - Heart and Circulatory Physiology",
issn = "0363-6135",
publisher = "American Physiological Society",
number = "6",
}