Cardioprotection via activation of protein kinase C-delta depends on modulation of the reverse mode of the Na+/Ca2+ exchanger

Circulation. 2006 Jul 4;114(1 Suppl):I226-32. doi: 10.1161/CIRCULATIONAHA.105.000570.

Abstract

Background: Pretreatment with the volatile anesthetic sevoflurane protects cardiomyocytes against subsequent ischemic episodes caused by a protein kinase C (PKC)-delta mediated preconditioning effect. Sevoflurane directly modulates cardiac Ca2+ handling, and because Ca2+ also serves as a mediator in other cardioprotective signaling pathways, possible involvement of the Na+/Ca2+ exchanger (NCX) in relation with PKC-delta in sevoflurane-induced cardioprotection was investigated.

Methods and results: Isolated right ventricular rat trabeculae were subjected to simulated ischemia and reperfusion (SI/R), consisting of superfusion with hypoxic glucose-free buffer for 40 minutes after rigor development, followed by reperfusion with normoxic glucose containing buffer. Preconditioning with sevoflurane before SI/R improved isometric force development during contractile recovery at 60 minutes after the end of hypoxic superfusion (83+/-7% [sevo] versus 57+/-2% [SI/R];n=8; P<0.01). Inhibition of the reverse mode of the NCX by KB-R7943 (10 micromol/L) or SEA0400 (1 micromol/L) during preconditioning attenuated the protective effect of sevoflurane. KB-R7943 and SEA0400 did not have intrinsic effects on the contractile recovery. Furthermore, inhibition of the NCX in trabeculae exposed to sevoflurane reduced sevoflurane-induced PKC-delta translocation toward the sarcolemma, as demonstrated by digital imaging fluorescent microscopy. The degree of PKC-delta phosphorylation at serine643 as determined by western blot analysis was not affected by sevoflurane.

Conclusions: Sevoflurane-induced cardioprotection depends on the NCX preceding PKC-delta translocation presumably via increased NCX-mediated Ca2+ influx. This may suggest that increased myocardial Ca2+ load triggers the cardioprotective signaling cascade elicited by volatile anesthetic agents similar to other modes of preconditioning.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anesthetics, Inhalation / pharmacology
  • Anesthetics, Inhalation / therapeutic use*
  • Aniline Compounds / pharmacology
  • Animals
  • Calcium Signaling / drug effects
  • Calcium Signaling / physiology*
  • Cardiotonic Agents / pharmacology
  • Cardiotonic Agents / therapeutic use*
  • Enzyme Activation
  • Glucose / pharmacology
  • Heart Ventricles / drug effects
  • Heart Ventricles / enzymology
  • In Vitro Techniques
  • Ischemic Preconditioning, Myocardial / methods*
  • Male
  • Methyl Ethers / pharmacology
  • Methyl Ethers / therapeutic use*
  • Myocardial Ischemia / enzymology*
  • Myocardial Reperfusion Injury / enzymology
  • Myocardial Reperfusion Injury / prevention & control*
  • Phenyl Ethers / pharmacology
  • Phosphorylation / drug effects
  • Phosphoserine / analysis
  • Protein Kinase C-delta / physiology*
  • Protein Processing, Post-Translational / drug effects
  • Protein Transport / drug effects
  • Rats
  • Rats, Wistar
  • Sarcolemma / enzymology
  • Sevoflurane
  • Signal Transduction / drug effects
  • Signal Transduction / physiology
  • Sodium-Calcium Exchanger / antagonists & inhibitors
  • Sodium-Calcium Exchanger / physiology*
  • Thiourea / analogs & derivatives
  • Thiourea / pharmacology

Substances

  • 2-(2-(4-(4-nitrobenzyloxy)phenyl)ethyl)isothiourea methanesulfonate
  • Anesthetics, Inhalation
  • Aniline Compounds
  • Cardiotonic Agents
  • Methyl Ethers
  • Phenyl Ethers
  • SEA 0400
  • Sodium-Calcium Exchanger
  • Phosphoserine
  • Sevoflurane
  • Protein Kinase C-delta
  • Thiourea
  • Glucose