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DOI 10.1152/ajpcell.00356.2015

Медицинская библиотека · American journal of physiology. Cell physiology · 2016

Chronology of mitochondrial and cellular events during skeletal muscle ischemia-reperfusion.

Paradis Stéphanie, Charles Anne-Laure, Meyer Alain, Lejay Anne, Scholey James W, Chakfé Nabil, Zoll Joffrey, Geny Bernard

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Аннотация

Peripheral artery disease (PAD) is a common circulatory disorder of the lower limb arteries that reduces functional capacity and quality of life of patients. Despite relatively effective available treatments, PAD is a serious public health issue associated with significant morbidity and mortality. Ischemia-reperfusion (I/R) cycles during PAD are responsible for insufficient oxygen supply, mitochondriopathy, free radical production, and inflammation and lead to events that contribute to myocyte death and remote organ failure. However, the chronology of mitochondrial and cellular events during the ischemic period and at the moment of reperfusion in skeletal muscle fibers has been poorly reviewed. Thus, after a review of the basal myocyte state and normal mitochondrial biology, we discuss the physiopathology of ischemia and reperfusion at the mitochondrial and cellular levels. First we describe the chronology of the deleterious biochemical and mitochondrial mechanisms activated by I/R. Then we discuss skeletal muscle I/R injury in the muscle environment, mitochondrial dynamics, and inflammation. A better understanding of the chronology of the events underlying I/R will allow us to identify key factors in the development of this pathology and point to suitable new therapies. Emerging data on mitochondrial dynamics should help identify new molecular and therapeutic targets and develop protective strategies against PAD.

Для цитирования: Paradis Stéphanie, Charles Anne-Laure, Meyer Alain, Lejay Anne, Scholey James W, Chakfé Nabil, Zoll Joffrey, Geny Bernard. Chronology of mitochondrial and cellular events during skeletal muscle ischemia-reperfusion.. American journal of physiology. Cell physiology. 2016. DOI: 10.1152/ajpcell.00356.2015.

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