Peripheral nociception associated with surgical incision elicits remote nonischemic cardioprotection via neurogenic activation of protein kinase C signaling

Circulation. 2009 Sep 15;120(11 Suppl):S1-9. doi: 10.1161/CIRCULATIONAHA.108.843938.

Abstract

Background: Although remote ischemic stimuli have been shown to elicit cardioprotection against ischemia/reperfusion injury, there is little known about the effects of nonischemic stimuli. We previously described a remote cardioprotective effect of nonischemic surgical trauma (abdominal incision) called remote preconditioning of trauma (RPCT). In the present study, we elucidate mechanisms underlying this phenomenon.

Methods and results: We used a murine model of myocardial infarction to evaluate ischemia/reperfusion injury, and either abdominal surgical incision, or application of topical capsaicin, to elicit cardioprotection. We show that the cardioprotective effect of RPCT is initiated by skin nociception, and requires neurogenic signaling involving spinal nerves and activation of cardiac sensory and sympathetic nerves. Our results demonstrate bradykinin-dependent activation and repression, respectively, of PKCepsilon and PKCdelta in myocardium after RPCT, and we show involvement of the K(ATP) channels in cardioprotection. Finally, we show that topical application of capsaicin, which selectively activates C sensory fibers in the skin, mimics the cardioprotective effect of RPCT against myocardial infarction.

Conclusions: Nontraumatic nociceptive preconditioning represents a novel therapeutic strategy for cardioprotection with great potential clinical utility.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Apoptosis
  • Capsaicin / pharmacology
  • Female
  • Heart / innervation*
  • Ischemic Preconditioning / methods*
  • KATP Channels / metabolism
  • Male
  • Mice
  • Myocardial Infarction / pathology
  • Myocardial Reperfusion Injury / prevention & control*
  • Pain / physiopathology*
  • Protein Kinase C / metabolism*
  • Signal Transduction*

Substances

  • KATP Channels
  • Protein Kinase C
  • Capsaicin