Targeting mitochondria for resuscitation from cardiac arrest

• Published in: Critical care medicine Vol. 36; no. 11; pp. S440 - S446
• Main Authors: AYOUB, Iyad M, RADHAKRISHNAN, Jeejabai, GAZMURI, Raul J
• Format: Conference Proceeding Journal Article
• Language: English
• Published: Hagerstown, MD Lippincott Williams & Wilkins 01-11-2008
• Subjects: Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy; Animals; Apoptosis; Biological and medical sciences; Calcium - metabolism; Cardiopulmonary Resuscitation; Cytochromes c - metabolism; Emergency and intensive cardiocirculatory care. Cardiogenic shock. Coronary intensive care; Heart Arrest - metabolism; Heart Arrest - physiopathology; Heart Arrest - therapy; Intensive care medicine; Medical sciences; Mitochondria - metabolism; Mitochondrial Membrane Transport Proteins - metabolism; Mitochondrial Membranes - metabolism; Mitochondrial Permeability Transition Pore; Myocardial Reperfusion Injury - metabolism; Myocardial Reperfusion Injury - physiopathology; Oxidative Phosphorylation; Resuscitation; Sodium - metabolism; Cardiocirculatory arrest; Mitochondria; Intensive care; cardiopulmonary resuscitation; Reperfusion; Targeting; Ischemia; Cardiovascular disease; reperfusion injury; Resuscitation
• ISSN: 0090-3493; 1530-0293
• DOI: 10.1097/ccm.0b013e31818a89f4

Reversal of cardiac arrest requires reestablishment of aerobic metabolism by reperfusion with oxygenated blood of tissues that have been ischemic for variable periods of time. However, reperfusion concomitantly activates a myriad of pathogenic mechanisms causing what is known as reperfusion injury. At the center of reperfusion injury are mitochondria, playing a critical role as effectors and targets of injury. Studies in animal models of ventricular fibrillation have shown that limiting myocardial cytosolic Na+ overload attenuates mitochondrial Ca2+ overload and maintains oxidative phosphorylation, which is the main bioenergetic function of mitochondria. This effect is associated with functional myocardial benefits such as preservation of myocardial compliance during chest compression and attenuation of myocardial dysfunction after return of spontaneous circulation. Additional studies in similar animal models of ventricular fibrillation have shown that mitochondrial injury leads to activation of the mitochondrial apoptotic pathway, characterized by the release of cytochrome c to the cytosol, reduction of caspase-9 levels, and activation of caspase-3 coincident with marked reduction in left ventricular function. Cytochrome c also "leaks" into the bloodstream attaining levels that are inversely proportional to survival. These data indicate that mitochondria play a key role during cardiac resuscitation by modulating energy metabolism and signaling apoptotic cascades and that targeting mitochondria could represent a promising strategy for cardiac resuscitation.