Succinate metabolism: a new therapeutic target for myocardial reperfusion injury

Cardiovasc Res. 2016 Jul 15;111(2):134-41. doi: 10.1093/cvr/cvw100. Epub 2016 May 18.

Abstract

Myocardial ischaemia/reperfusion (IR) injury is a major cause of death worldwide and remains a disease for which current clinical therapies are strikingly deficient. While the production of mitochondrial reactive oxygen species (ROS) is a critical driver of tissue damage upon reperfusion, the precise mechanisms underlying ROS production have remained elusive. More recently, it has been demonstrated that a specific metabolic mechanism occurs during ischaemia that underlies elevated ROS at reperfusion, suggesting a unifying model as to why so many different compounds have been found to be cardioprotective against IR injury. This review will discuss the role of the citric acid cycle intermediate succinate in IR pathology focusing on the mechanism by which this metabolite accumulates during ischaemia and how it can drive ROS production at Complex I via reverse electron transport. We will then examine the potential for manipulating succinate accumulation and metabolism during IR injury in order to protect the heart against IR damage and discuss targets for novel therapeutics designed to reduce reperfusion injury in patients.

Keywords: Ischaemia/reperfusion; Mitochondria; Reactive oxygen species; Succinate.

Publication types

  • Review

MeSH terms

  • Animals
  • Cardiovascular Agents / pharmacology
  • Electron Transport
  • Electron Transport Complex I / metabolism
  • Electron Transport Complex II / metabolism
  • Energy Metabolism* / drug effects
  • Humans
  • Myocardial Reperfusion Injury / drug therapy
  • Myocardial Reperfusion Injury / metabolism*
  • Myocardial Reperfusion Injury / pathology
  • Myocardial Reperfusion Injury / physiopathology
  • Myocardium / metabolism*
  • Myocardium / pathology
  • Reactive Oxygen Species / metabolism
  • Signal Transduction
  • Succinic Acid / metabolism*

Substances

  • Cardiovascular Agents
  • Reactive Oxygen Species
  • Succinic Acid
  • Electron Transport Complex II
  • Electron Transport Complex I