The Effects of Potassium Cyanide on the Functional Recovery of Isolated Rat Hearts after Ischemia and Reperfusion: The Role of Oxidative Stress.
Anica M PetkovicJakovljevic Lj VladimirJovana V BradicJovana N JeremićNevena S JeremićTamara R Nikolic TurnicNemanja U JovicicVesna Z RosicIvan M SrejovicVladimir I ZivkovicPublished in: Oxidative medicine and cellular longevity (2018)
This investigation is aimed at examining the effects of pharmacological PostC with potassium cyanide (KCN) on functional recovery, gene expression, cytochrome c expression, and redox status of isolated rat hearts. Rats were divided into the control and KCN groups. The hearts of male Wistar albino rats were retrogradely perfused according to the Langendorff technique at a constant perfusion pressure of 70 cmH2O. After stabilisation, control hearts were subjected to global ischemia (5 minutes), followed by reperfusion (5 minutes), while experimental hearts underwent global ischemia (5 minutes) followed by 5 minutes of reperfusion with 10 μmol/L KCN. The following parameters of heart function were measured: maximum and minimum rates of pressure development, systolic and diastolic left ventricular pressure, heart rate, and coronary flow. Levels of superoxide anion radical, hydrogen peroxide, nitrites, and index of lipid peroxidation (measured as thiobarbituric acid-reactive substances) were measured in coronary venous effluent, and activity of catalase was determined in heart tissue. Expression of Bax, Bcl-2, SOD-1, SOD-2, and cytochrome c was studied as well. It was shown that expression of Bax, Bcl-2, and SOD-2 genes did not significantly differ between groups, while expression of SOD-1 gene and cytochrome c was lower in the KCN group. Our results demonstrated that KCN improved the recovery of myocardial contractility and systolic and diastolic function, enhanced catalase activity, and diminished generation of prooxidants. However, all possible mechanisms and potential adverse effects of KCN should be further examined in the future.
Keyphrases
- left ventricular
- blood pressure
- poor prognosis
- hydrogen peroxide
- acute myocardial infarction
- heart rate
- oxidative stress
- heart failure
- gene expression
- aortic stenosis
- coronary artery disease
- genome wide
- hypertrophic cardiomyopathy
- amyotrophic lateral sclerosis
- cerebral ischemia
- dna methylation
- magnetic resonance imaging
- binding protein
- left atrial
- heart rate variability
- long non coding rna
- drinking water
- induced apoptosis
- brain injury
- mitral valve
- copy number
- ejection fraction
- magnetic resonance
- human health
- climate change
- subarachnoid hemorrhage
- fluorescent probe
- transcatheter aortic valve replacement