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

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          Abstract

          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.

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          Author and article information

          Journal
          Am J Physiol Cell Physiol
          Am. J. Physiol., Cell Physiol
          ajpcell
          ajpcell
          AJPCELL
          American Journal of Physiology - Cell Physiology
          American Physiological Society (Bethesda, MD )
          0363-6143
          1522-1563
          1 June 2016
          1 June 2017
          : 310
          : 11
          : C968-C982
          Affiliations
          [1] 1University of Strasbourg, Fédération de Médecine Translationelle, EA 3072, Strasbourg, France;
          [2] 2Department of Physiology and Functional Explorations, Thoracic Pathology Unit, Centre Hospitalier Régional Universitaire de Strasbourg, Strasbourg, France;
          [3] 3Department of Vascular Surgery and Kidney Transplantation, Centre Hospitalier Régional Universitaire de Strasbourg, Strasbourg, France; and
          [4] 4Department of Medicine and Institute of Medical Science, University of Toronto, Toronto, Ontario, Canada
          Author notes
          Address for reprint requests and other correspondence: S. Paradis, Faculté de Médecine, Institut de Physiologie, EA3072 “Mitochondrie, stress oxydant et protection musculaire,” 11 Rue Humann, 67085 Strasbourg Cedex, France (e-mail: sparadis@ 123456unistra.fr ).
          Article
          PMC4935201 PMC4935201 4935201 C-00356-2015
          10.1152/ajpcell.00356.2015
          4935201
          27076618
          9a0b1ff3-3d5d-4c86-af8a-222e78a7c1de
          Copyright © 2016 the American Physiological Society
          History
          Categories
          Review

          oxidative stress,skeletal muscle,ischemia-reperfusion,peripheral artery disease,mitochondria

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