Effects of sevoflurane preconditioning and postconditioning on rat myocardial stunning in ischemic reperfusion injury
- PMID: 20349523
- PMCID: PMC2852543
- DOI: 10.1631/jzus.B0900390
Effects of sevoflurane preconditioning and postconditioning on rat myocardial stunning in ischemic reperfusion injury
Abstract
Ischemic preconditioning and postconditioning distinctly attenuate ventricular arrhythmia after ischemia without affecting the severity of myocardial stunning. Therefore, we report the effects of sevoflurane preconditioning and postconditioning on stunned myocardium in isolated rat hearts. Isolated rat hearts were underwent 20 min of global ischemia and 40 min of reperfusion. After an equilibration period (20 min), the hearts in the preconditioning group were exposed to sevoflurane for 5 min and next washout for 5 min before ischemia. Hearts in the sevoflurane postconditioning group underwent equilibration and ischemia, followed immediately by sevoflurane exposure for the first 5 min of reperfusion. The control group received no treatment before and after ischemia. Left ventricular pressure, heart rate, coronary flow, electrocardiogram, and tissue histology were measured as variables of ventricular function and cellular injury, respectively. There was no significant difference in the duration of reperfusion ventricular arrhythmias between control and sevoflurane preconditioning group (P=0.195). The duration of reperfusion ventricular arrhythmias in the sevoflurane postconditioning group was significantly shorter than that in the other two groups (P<0.05). +/-(dP/dt)(max) in the sevoflurane preconditioning group at 5, 10, 15, 20, and 30 min after reperfusion was significantly higher than that in the control group (P<0.05), and there were no significant differences at 40 min after reperfusion among the three groups (P>0.05). As expected, for a 20-min general ischemia, infarct size in heart slices determined by 2,3,5-triphenyltetrazolium chloride staining among the groups was not obvious. Sevoflurane postconditioning reduces reperfusion arrhythmias without affecting the severity of myocardial stunning. In contrast, sevoflurane preconditioning has no beneficial effects on reperfusion arrhythmias, but it is in favor of improving ventricular function and recovering myocardial stunning. Sevoflurane preconditioning and postconditioning may be useful for correcting the stunned myocardium.
Figures







Similar articles
-
Sevoflurane postconditioning reduces myocardial reperfusion injury in rat isolated hearts via activation of PI3K/Akt signaling and modulation of Bcl-2 family proteins.J Zhejiang Univ Sci B. 2010 Sep;11(9):661-72. doi: 10.1631/jzus.B1000155. J Zhejiang Univ Sci B. 2010. PMID: 20803770 Free PMC article.
-
Sevoflurane postconditioning converts persistent ventricular fibrillation into regular rhythm.Eur J Anaesthesiol. 2009 Sep;26(9):766-71. doi: 10.1097/EJA.0b013e32832a58fa. Eur J Anaesthesiol. 2009. PMID: 19367168
-
Anesthetic preconditioning combined with postconditioning offers no additional benefit over preconditioning or postconditioning alone.Anesth Analg. 2007 Aug;105(2):316-24. doi: 10.1213/01.ane.0000267524.71445.e7. Anesth Analg. 2007. PMID: 17646483
-
Interaction of cardiovascular risk factors with myocardial ischemia/reperfusion injury, preconditioning, and postconditioning.Pharmacol Rev. 2007 Dec;59(4):418-58. doi: 10.1124/pr.107.06002. Epub 2007 Nov 29. Pharmacol Rev. 2007. PMID: 18048761 Review.
-
Protective effect of sevoflurane on myocardial ischemia-reperfusion injury: a systematic review and meta-analysis.Int J Surg. 2024 Nov 1;110(11):7311-7330. doi: 10.1097/JS9.0000000000001975. Int J Surg. 2024. PMID: 39093878 Free PMC article.
Cited by
-
Comparison of the effects of sevoflurane and propofol anesthesia on pulmonary function, MMP-9 and postoperative cognition in patients receiving lung cancer resection.Oncol Lett. 2019 Mar;17(3):3399-3405. doi: 10.3892/ol.2019.9993. Epub 2019 Jan 30. Oncol Lett. 2019. PMID: 30867776 Free PMC article.
-
Late Post-Conditioning with Sevoflurane after Cardiac Surgery--Are Surrogate Markers Associated with Clinical Outcome?PLoS One. 2015 Jul 21;10(7):e0132165. doi: 10.1371/journal.pone.0132165. eCollection 2015. PLoS One. 2015. PMID: 26196133 Free PMC article. Clinical Trial.
-
Effects of Sevoflurane on Apoptosis of Myocardial Cells in IRI Rats.Biomed Res Int. 2021 Dec 31;2021:3347949. doi: 10.1155/2021/3347949. eCollection 2021. Biomed Res Int. 2021. Retraction in: Biomed Res Int. 2024 Mar 20;2024:9853194. doi: 10.1155/2024/9853194. PMID: 35005016 Free PMC article. Retracted.
-
Pharmacological postconditioning with diazoxide attenuates ischemia/reperfusion-induced injury in rat liver.Exp Ther Med. 2013 Apr;5(4):1169-1173. doi: 10.3892/etm.2013.941. Epub 2013 Jan 31. Exp Ther Med. 2013. PMID: 23596486 Free PMC article.
-
Protective Effect of Sevoflurane Preconditioning on Cardiomyocytes Against Hypoxia/Reoxygenation Injury by Modulating Iron Homeostasis and Ferroptosis.Cardiovasc Toxicol. 2023 Feb;23(2):86-92. doi: 10.1007/s12012-023-09782-w. Epub 2023 Feb 17. Cardiovasc Toxicol. 2023. PMID: 36800141
References
-
- Bolli R, Marban E. Molecular and cellular mechanisms of myocardial stunning. Physiol Rev. 1999;79(2):609–634. - PubMed
-
- Bouwman RA, Salic K, Padding FG, Eringa EC, van Beek-Harmsen BJ, Matsuda T, Baba A, Musters RJ, Paulus WJ, de Lange JJ, et al. Cardioprotection via activation of protein kinase C-delta depends on modulation of the reverse mode of the Na+/Ca2+ exchanger. Circulation. 2006;114(1Suppl.):I226–I232. doi: 10.1161/CIRCULATIONAHA.105.000570. - DOI - PubMed
-
- Braunwald E, Kloner RA. The stunned myocardium: prolonged, postischemic ventricular dysfunction. Circulation. 1982;66(6):1146–1149. - PubMed
-
- Chiari PC, Bienengraeber MW, Pagel PS, Krolikowski JG, Kersten JR, Warltier DC. Isoflurane protects against myocardial infarction during early reperfusion by activation of phosphatidylinositol-3-kinase signal transduction: evidence for anesthetic-induced postconditioning in rabbits. Anesthesiology. 2005;102(1):102–109. doi: 10.1097/00000542-200501000-00018. - DOI - PubMed
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Research Materials