Nuclear factor-kappa B inhibition provides additional protection against ischaemia/reperfusion injury in delayed sevoflurane preconditioning

作者：Konia Mojca Remskar; Schaefer Saul; Liu Hong^*

来源：European Journal of Anaesthesiology, 2009, 26(6): 496-503.

DOI：10.1097/EJA.0b013e328324ed2e

• delayed preconditioning
• myocardium
• nuclear factor-kappa B
• rat
• sevoflurane

Background and objective Sevoflurane anaesthetic preconditioning (SPC) has been shown to limit nuclear factor-kappa B (NF-kappa B) activation and the production of inflammatory cytokines during myocardial ischaemia/reperfusion (I/R). Similarly, pharmacological inhibition of NF-kappa B using parthenolide is effective in limiting I/R We, therefore, postulated that the protective effect of delayed SPC would be enhanced by pharmacological NF-kappa B inhibition during I/R.
Methods Hearts from 2-month-old male Fisher 344 rats were exposed to 25 min global ischaemia followed by 60 min reperfusion. Rats were divided into four groups to I/R: control group; parthenolide group, treated with the I kappa B kinase inhibitor parthenolide intraperitoneally 10 min prior to heart isolation; SPC group, treated for 60 min sevoflurane 48h prior to heart isolation; and SPC + parthenolide group, treated with SPC for 1h by parthenolide 48h later. Infarct area, left ventricular function and Ca(2+) were measured after I/R.
Results Delayed SPC + parthenolide resulted in greater protection than either intervention alone, resulting in a significant reduction in infarct area and left ventricular developed pressure (mmHg; 84 +/- 19 compared with 15 +/- 14 in control hearts; P = 0.007). Left ventricular end-diastolic pressure also remained close to baseline values (9 +/- 2 mmHg, P = 0.02) during I/R, and the increase in Ca(2+) seen with I/R was significantly blunted (P = 0.005).
Conclusion SPC followed by parthenolide provides a significant protection from I/R injury in this model. As each intervention alone limits NF-kappa B activation with I/R, these data are consistent with additive effects of these dual modalities in limiting I/R injury due to NF-kappa B activation.

• 出版日期2009-6