Remote ischaemic pre- and delayed postconditioning - similar degree of cardioprotection but distinct mechanisms

Exp Physiol. 2012 Aug;97(8):908-17. doi: 10.1113/expphysiol.2012.064923. Epub 2012 Mar 16.

Abstract

Myocardial ischaemia-reperfusion injury can be significantly reduced by an episode(s) of ischaemia-reperfusion applied prior to or during myocardial ischaemia (MI) to peripheral tissue located at a distance from the heart; this phenomenon is called remote ischaemic conditioning (RIc). Here, we compared the efficacy of RIc in protecting the heart when the RIc stimulus is applied prior to, during and at different time points after MI. A rat model of myocardial ischaemia-reperfusion injury involved 30 min of left coronary artery occlusion followed by 120 min of reperfusion. Remote ischaemic conditioning was induced by 15 min occlusion of femoral arteries and conferred a similar degree of cardioprotection when applied 25 min prior to MI, 10 or 25 min after the onset of MI, or starting 10 min after the onset of reperfusion. These RIc stimuli reduced infarct size by 54, 56, 56 and 48% (all P < 0.001), respectively. Remote ischaemic conditioning applied 30 min into the reperfusion period was ineffective. Activation of sensory nerves by application of capsaicin was effective in establishing cardioprotection only when elicited prior to MI. Vagotomy or denervation of the peripheral ischaemic tissue both completely abolished cardioprotection induced by RIc applied prior to MI. Cardioprotection conferred by delayed remote postconditioning was not affected by either vagotomy or peripheral denervation. These results indicate that RIc confers potent cardioprotection even if applied with a significant delay after the onset of myocardial reperfusion. Cardioprotection by remote preconditioning is critically dependent on afferent innervation of the remote organ and intact parasympathetic activity, while delayed remote postconditioning appears to rely on a different signalling pathway(s).

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Capsaicin / pharmacology
  • Femoral Artery / physiopathology
  • Heart / drug effects
  • Heart / innervation
  • Heart / physiopathology
  • Ischemic Postconditioning / methods*
  • Ischemic Preconditioning, Myocardial / methods*
  • Male
  • Myocardial Infarction / drug therapy
  • Myocardial Infarction / prevention & control*
  • Myocardial Reperfusion Injury / drug therapy
  • Myocardial Reperfusion Injury / prevention & control*
  • Rats
  • Rats, Wistar
  • Sensory System Agents / pharmacology
  • Vagotomy

Substances

  • Sensory System Agents
  • Capsaicin