Effect of isoflurane delayed preconditioning on myocardial ischemia reperfusion injury in rabbits.
- Author:
Ke RAN
1
;
Kai-ming DUAN
;
Ding-quan ZOU
;
Zhi-jian LI
;
Li-yan JIN
;
Ye-tian CHANG
Author Information
1. Department of Anesthesilogy, Second Xiangya Hospital,Central South University,Changsha, China. rankerk@126.com
- Publication Type:Journal Article
- MeSH:
Animals;
Ischemic Preconditioning, Myocardial;
methods;
Isoflurane;
pharmacology;
Male;
Myocardial Reperfusion Injury;
pathology;
prevention & control;
Myocardium;
ultrastructure;
Rabbits;
Random Allocation;
Tumor Necrosis Factor-alpha;
metabolism;
p38 Mitogen-Activated Protein Kinases;
metabolism
- From:
Journal of Central South University(Medical Sciences)
2008;33(2):146-150
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVE:To investigate the protective effect of isoflurane delayed preconditioning on myocardial ischemia reperfusion injury and the potential mechanism in rabbits.
METHODS:Thirty New Zealand male white rabbits were randomly assigned to 3 groups: Control group; I/R group; and 2.0% isoflurane group. Isoflurane group was exposed to 2.0% isoflurane-100% oxygen for 2 hours. Control group and I/R group were exposed to 100% oxygen for 2 hours and served as untreated controls. Twenty-four hours later I/R group and isoflurane group underwent 40 minutes of coronary occlusion followed by 2 hours of reperfusion. Blood samples were taken from the arterial line at 20 minutes before the occlusion(T1), 20 minutes after the occlusion(T2), 40 minutes after the occlusion(T3), 1 hours after the reperfusion(T4), and 2 hours after the reperfusion(T5) to determine the plasma level of TNF-alpha. At the end of the reperfusion, infarct size and area at risk were defined by Evans and TTC staining. The heart was harvested and levels of the p38MAPK activity were determined by Western blot, and ultrastructures were observed under the electron microscope.
RESULTS:The p38MAPK activity of isoflurane group was significantly lower than that of I/R group (P<0.05). Isoflurane significantly (P<0.05) reduced the infarct size(19.7%+/-2.8% in isoflurane group) of the left ventricular area at risk as compared with the controls (37.8%+/-1.7% in I/R group).The injury of I/R group was worse than that of isoflurane group under the light microscope. Isoflurane group had a lower level of TNF-alpha than I/R group.
CONCLUSION:Isoflurane can inhibit p38MAPK activity during myocardial ischemia reperfusion and modulate the cytokine expression, which may be one of the molecular mechanisms of isoflurane delayed preconditioning on cardioprotection.
