Journal article
Role of protein kinase C-ε (PKCε) in isoflurane-induced cardioprotection
British journal of anaesthesia : BJA, Vol.94(2), pp.166-173
02/01/2005
DOI: 10.1093/bja/aei022
PMID: 15542537
Abstract
Background. Volatile anaesthetics precondition the heart against infarction, an effect partly mediated by activation of the ε isoform of protein kinase C (PKCε). We investigated whether cardioprotection by activation of PKCε depends on the isoflurane concentration. Methods. Anaesthetized rats underwent 25 min of coronary artery occlusion followed by 120 min of reperfusion and were randomly assigned to the following groups (n=10 in each group): isoflurane preconditioning induced by 15 min administration of 0.4 minimal alveolar concentration (MAC) (0.4MAC), 1 MAC (1MAC) or 1.75 MAC (1.75MAC) followed by 10 min washout before ischaemia. Each protocol was repeated in the presence of the PKC inhibitor staurosporine (10 µg kg−1): 0.4MAC+S, 1MAC+S and 1.75MAC+S. Controls were untreated (CON) and additional hearts received staurosporine without isoflurane (S). In a second set of experiments (n=6 in each group) hearts were excised before the infarct inducing ischaemia, and phosphorylation and translocation of PKCε were determined by western blot analysis. Results. Isoflurane reduced infarct size from a mean of 61(SEM 2)% of the area at risk in controls to 20(1)% (0.4MAC), 26(3)% (1MAC) and 30(1)% (1.75MAC) (all P<0.01 vs CON or S). This protection was partially reversed by administration of staurosporine in the 0.4MAC+S group (30[2]%; P<0.05 vs 0.4MAC) group, but not after administration of 1 MAC or 1.75 MAC isoflurane (26[2]% and 31[2]%, respectively). Thus 0.4MAC increased PKCε phosphorylation, and this effect was blocked by staurosporine. Higher concentrations of isoflurane did not change PKCε phosphorylation. PKCε was translocated to the membrane fraction after administration of 0.4 MAC isoflurane, but not after 1.0 or 1.75 MAC. Conclusions. Although isoflurane preconditioning resulted in a reduction in infarct size at all concentrations used, the protection was mediated by phosphorylation and translocation of PKCε only at 0.4 MAC.
Details
- Title: Subtitle
- Role of protein kinase C-ε (PKCε) in isoflurane-induced cardioprotection
- Creators
- D. Obal - Heinrich Heine University DüsseldorfN. C. Weber - Heinrich Heine University DüsseldorfK. Zacharowski - Heinrich Heine University DüsseldorfO. Toma - Heinrich Heine University DüsseldorfS. Dettwiler - Heinrich Heine University DüsseldorfJ. I. Wolter - Heinrich Heine University DüsseldorfM. Kratz - Heinrich Heine University DüsseldorfJ. Müllenheim - Department of Anesthesiology, University Hospital, Moorenstraße 5, 40225 Düsseldorf, GermanyB. Preckel - Heinrich Heine University DüsseldorfW. Schlack - Heinrich Heine University Düsseldorf
- Resource Type
- Journal article
- Publication Details
- British journal of anaesthesia : BJA, Vol.94(2), pp.166-173
- DOI
- 10.1093/bja/aei022
- PMID
- 15542537
- NLM abbreviation
- Br J Anaesth
- ISSN
- 0007-0912
- eISSN
- 1471-6771
- Publisher
- Oxford University Press
- Language
- English
- Date published
- 02/01/2005
- Academic Unit
- Anesthesia
- Record Identifier
- 9984696582102771
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