Ellagic Acid Protects Cardiac Arrhythmias Following Global Cerebral Ischemia/Reperfusion Model

Authors

  • Khojasteh Hoseiny Nejad Abadan Arvand International Division, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran
  • Mahin Dianat 1.Physiology Research Center, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran 2.Department of Physiology, Faculty of Medicine, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran
  • Alireza Sarkaki 1.Physiology Research Center, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran 2.Department of Physiology, Faculty of Medicine, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran
  • Yaghoub Farbood 1.Physiology Research Center, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran 2.Department of Physiology, Faculty of Medicine, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran
  • Mohammad Badavi 1.Physiology Research Center, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran 2.Department of Physiology, Faculty of Medicine, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran
  • Mohammad Kazem Gharib-Naseri Physiology Research Center, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran

DOI:

https://doi.org/10.31661/gmj.v8i.1235

Keywords:

Ellagic Acid, Ischemia/Reperfusion, Arrhythmias

Abstract

Background: Cerebral ischemia/reperfusion (I/R) could increase the reactive oxidative stress in the cardiomyocytes. Also, some studies report cardiac arrhythmias following oxidative stressor such as I/R. Hence, this study was aimed to investigate the effects of ellagic acid (EA) against arrhythmias in a cerebral I/R model. Materials and Methods: Thirty-two male rats were randomly allocated into four groups: Sham (normal saline, 10 days), EA (100 mg/kg EA, 10 days), I/R (20 min ischemia followed by 30 min reperfusion, 10 days), and EA + I/R (100 mg/kg EA before I/R). In all animals, electrocardiogram (ECG) was recorded pre-ischemia and postischemia on the first and 11th days, respectively. Results: The I/R group showed an abnormally prolonged QTc interval after ischemia compared to the preischemia and control groups. EA administration in the EA+I/R group significantly reduced this prolonged QTc interval (P< 0.01). In the I/R group, ischemic/reperfusion resulted in a prolonged QRS complex and an elevated ST, which EA significantly prevented (P<0.01). In addition, EA significantly prevented the dramatically shortened RR interval induced by reperfusion (P<0.01). The incidence of ventricular fibrillation significantly increased in the I/R group; then it dramatically decreased following the administration of EA (P<0.0001). Conclusion: EA pretreatment repaired the adverse effects of I/R on the ECG parameters, which can be attributed to its negative chronotropic effects. EA pretreatment can prevent the cerebral I/R-induced heart arrhythmias.
[GMJ.2019;8:e1235]

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Published

2019-02-25

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Original Article