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Methods for the Determination of Rates of Glucose and Fatty Acid Oxidation in the Isolated Working Rat Heart
Published on: September 28, 2016
Cardioprotection by intermittent fasting in rats
Ismayil Ahmet1, Ruiqian Wan, Mark P Mattson
1Laboratory of Cardiovascular Sciences, National Institute on Aging, Intramural Research Program, National Institutes of Health, Baltimore, MD, USA.
Circulation
|November 9, 2005
Summary
Intermittent fasting (IF) significantly reduces heart damage and cardiac remodeling after myocardial infarction in rats. This dietary strategy offers cardioprotective benefits by reducing inflammation and cell death.
Area of Science:
- Cardiology
- Metabolic research
- Neuroprotection
Background:
- Intermittent fasting (IF) is a dietary pattern involving cycles of eating and voluntary fasting.
- IF has demonstrated life-extending and disease-reducing effects in rodent models.
- Previous research indicated neuroprotective properties of IF against ischemic brain injury.
Purpose of the Study:
- To investigate the protective effects of intermittent fasting on cardiac ischemic injury in a rat model.
- To evaluate the impact of IF on myocardial infarction (MI) size and subsequent cardiac remodeling.
Main Methods:
- Rats were placed on either an IF diet or a regular feeding schedule for 3 months.
- Myocardial infarction was induced by coronary artery ligation.
- Cardiac function, size, apoptotic cell count, and inflammatory response were assessed post-MI.
Main Results:
- IF significantly reduced the size of myocardial infarction by 2-fold compared to controls.
- The number of apoptotic myocytes in the area at risk was 4-fold lower in the IF group.
- IF attenuated left ventricular remodeling and expansion post-MI, preserving cardiac function.
Conclusions:
- Intermittent fasting confers significant protection against acute ischemic heart injury.
- IF effectively mitigates adverse cardiac remodeling following myocardial infarction.
- The cardioprotective mechanisms of IF likely involve antiapoptotic and anti-inflammatory pathways.

