A New Model of Heart Failure Post-Myocardial Infarction in the Rat

Honglei Li1, Jiansheng Huang2, Caihong Liu3

  • 1College of Traditional Chinese Medicine, Shandong University of Traditional Chinese Medicine; Department of Intensive Care Unit, Jinan Municipal Hospital of Traditional Chinese Medicine.

Insights

This study presents a new, reliable rat model for heart failure (HF) after myocardial infarction (MI) without requiring a ventilator. This improved model shows reduced variability, aiding research into HF mechanisms and drug development.

Area of Science:

  • Cardiovascular Research
  • Animal Models
  • Myocardial Infarction

Background:

  • The rat model of heart failure (HF) post myocardial infarction (MI) using left anterior descending (LAD) coronary artery ligation is common.
  • Existing models suffer from high mortality, variability in infarct size and cardiac function, and procedural complexity requiring ventilation or heart exteriorization.

Purpose of the Study:

  • To develop a reliable and reproducible rat model of HF post-MI without the need for a ventilator or heart exteriorization.
  • To establish a standardized method for inducing MI and subsequent HF in rats for research purposes.

Main Methods:

  • Ligation of the LAD coronary artery in rats without using a ventilator or exteriorizing the heart.
  • Assessment of cardiac function and damage four weeks post-procedure using serum biomarkers (CK-MB, NT-proBNP, Renin) and left ventricle ejection fraction (LVEF).
  • Quantitative analysis of infarct size and cardiac fibrosis using TTC and Masson's trichrome staining.

Main Results:

  • Significantly elevated serum CK-MB, NT-proBNP, and Renin levels in the MI group compared to the sham group.
  • Markedly reduced LVEF in the MI group, indicating impaired cardiac function.
  • Consistent infarct size and cardiac fibrosis area with smaller variations in the MI group, confirming model reproducibility.

Conclusions:

  • The developed LAD ligation method provides a reliable and reproducible rat model for HF post-MI.
  • This model minimizes procedural complications and variability, making it suitable for studying MI/HF mechanisms.
  • The model is valuable for preclinical drug development and testing pharmacological strategies for MI and HF treatment in rats.

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