A subscription to JoVE is required to view this content. Sign in or start your free trial.
* These authors contributed equally
Here, we describe an experimental model of myocardial infarction, an echocardiography procedure to study cardiac remodeling and function, and procedures for quantifying fibrosis and hypertrophy in picrosirius red-stained and rhodamine-stained sections, as well as the infarct size and expansion index in slices stained with Masson's trichrome.
Cardiovascular disease is the most prevalent cause of death in Western countries, with acute myocardial infarction (MI) being the most prevalent form. This paper describes a protocol for studying the role of galectin 3 (Gal-3) in the temporal evolution of cardiac healing and remodeling in an experimental animal model of MI.
The procedures described include an experimental model of MI with a permanent coronary ligature in male C57BL/6J (control) and Gal-3 knockout (KO) mice, an echocardiography procedure to study cardiac remodeling and systolic function in vivo, a histological evaluation of interstitial myocardial fibrosis with picrosirius red-stained and rhodamine-conjugated lectin-stained sections for studying myocyte hypertrophy by the cross-sectional area (MCSA), and the quantification of infarct size and cardiac remodeling (scar thinning, septum thickness, and expansion index) by planimetry in slices stained with Masson's trichrome and triphenyl tetrazolium chloride. Gal-3 KO mice with MI showed disrupted cardiac remodeling and an increase in the scar thinning ratio and the expansion index. At the onset of MI, myocardial function and cardiac remodeling were also severely affected. At 4 weeks post MI, the natural evolution of fibrosis in infarcted Gal-3 KO mice was also affected.
In summary, the experimental model of MI is a suitable model for studying the temporal evolution of cardiac repair and remodeling in mice with the genetic deletion of Gal-3 and other animal models. The lack of Gal-3 affects the dynamics of cardiac repair and disrupts the evolution of cardiac remodeling and function after MI.
Myocardial infarction (MI) is the most prevalent form of cardiovascular disease. After MI, the myocardium undergoes serial morphological and functional changes, including the healing of the MI infarct zone, ventricular remodeling (VR), and myocardial dysfunction1. The healing of MI is a dynamic and well-orchestrated process associated with profound inflammatory infiltration that ends in the formation of a fibrotic scar2,3. The experimental model of MI in mice is currently used for studying cardiac remodeling under pathological conditions4,
NOTE: All the experiments described in this protocol were approved by the Animal Care and Research Committee of the University of Buenos Aires (CICUAL), in line with the National Research Council (US) Committee for the Update of the Guide for the Care and Use of Laboratory Animals13. For the experiments, use male, age-matched C57BL/6J and Gal-3 KO mice (8-10 weeks old) weighing 30-35 g, which allow for better manipulation for surgery. Allow the animals access to water and food ad libi.......
Post-MI survival and necropsy
Over 4 weeks of follow-up, 17% (4/23) of the C57 mice versus 40% (8/20) of the Gal-3 KO mice were found dead. The necropsy was performed; the dead Gal-3 KO mice showed larger hearts than the C57 mice (Figure 1), and 38% of the C57 mice compared with 32% of the Gal-3 KO mice had macroscopic chest clots that were directly associated with cardiac rupture. The latter demonstrated that the cause of death was not relat.......
The experimental model of MI by permanent coronary artery ligature is used for studying a wide variety of pathophysiological mechanisms of cardiac repair and remodeling5,14,17. This article summarizes different methods currently used in this laboratory for studying the temporal evolution of cardiac repair and its effects on post-MI ventricular remodeling14,17. Two models.......
The authors gratefully appreciate the technical assistance of Ana Chiaro. This work was supported by grants from the Argentinean Agency for Promotion of Science and Technology (PICT 2014-2320, 2019-02987 and PICT 2018-03267 to VM) and the University of Buenos Aires (UBACyT 2018- 382 20020170100619BA to GEG).
....Name | Company | Catalog Number | Comments |
8-0 silk suture | Ethicon | ||
C57BL/6J mice | Department of Bioresources of the Faculty of Veterinary of the University of Buenos Aires, Argentina | ||
Forceps | |||
Hardvard 386 respirator | Hardvard company | ||
Heating pad | maintain animal's temperature during surgery | ||
Image Pro-Plus 6.0 | Media Cybernetics | Image Analysis Software | |
Ketamine | Holiday | ||
Masson Trichrome | BIOPUR | ||
Picrosirius red | BIOPUR | ||
Retractors | |||
Rodent Ventilator Model 683 | Harvard Apparatus | Mechanical ventilator | |
Scissors | |||
Stereoscopic magnifying glass | Arcano | ||
Vivid 7 machine (General Electric Medical Systems, Horten, Norway) | General Electric | Any tracking software can be utilized with this protocol | |
WGA no. RL-1022, Vector Laboratories, Burlingame | Vector Laboratories | ||
Xylazine | Pro-Ser |
This article has been published
Video Coming Soon
ABOUT JoVE
Copyright © 2024 MyJoVE Corporation. All rights reserved