[Ischemia-reperfusion injury after lung transplantation]

Presse Med. 2014 Sep;43(9):921-30. doi: 10.1016/j.lpm.2014.01.018. Epub 2014 Jun 13.
[Article in French]

Abstract

Lung ischemia-reperfusion is characterized by diffuse alveolar damage arising from the first hours after transplantation. The first etiology of the primary graft dysfunction in lung is ischemia-reperfusion. It is burdened by an important morbi-mortality. Lung ischemia-reperfusion increases the oxidative stress, inactivates the sodium pump, increases the intracellular calcium, leads to cellular death and the liberation of pro-inflammatory mediators. Researches relative to the reduction of the lung ischemia-reperfusion injuries are numerous but few of them found a place in common clinical practice, because of an insufficient level of proofs. Ex vivolung evaluation is a suitable technique in order to evaluate therapeutics supposed to limit lung ischemia-reperfusion injuries.

Publication types

  • Review

MeSH terms

  • Adenosine Triphosphate / metabolism
  • Apoptosis
  • Bronchodilator Agents / therapeutic use
  • Calcium / metabolism
  • Carbon Monoxide / therapeutic use
  • Cytokines / metabolism
  • Humans
  • Ischemic Postconditioning
  • Ischemic Preconditioning
  • Lung Transplantation / adverse effects*
  • Mitochondrial Membrane Transport Proteins / metabolism
  • NADPH Oxidases / metabolism
  • Nitric Oxide / metabolism
  • Nitric Oxide / therapeutic use
  • Organ Preservation
  • Oxidative Stress / physiology
  • Oxygen / administration & dosage
  • Pulmonary Alveoli / blood supply
  • Pulmonary Surfactants / therapeutic use
  • Reactive Oxygen Species / metabolism
  • Reperfusion / methods
  • Reperfusion Injury / etiology*
  • Reperfusion Injury / physiopathology
  • Reperfusion Injury / prevention & control
  • Respiration, Artificial / methods
  • Severity of Illness Index
  • Sodium-Potassium-Exchanging ATPase / metabolism

Substances

  • Bronchodilator Agents
  • Cytokines
  • Mitochondrial Membrane Transport Proteins
  • Pulmonary Surfactants
  • Reactive Oxygen Species
  • Nitric Oxide
  • Carbon Monoxide
  • Adenosine Triphosphate
  • NADPH Oxidases
  • Sodium-Potassium-Exchanging ATPase
  • Oxygen
  • Calcium