Sevoflurane Postconditioning Mitigates Cerebral Ischemia-Reperfusion Injury in Rats

被引:0
|
作者
Li, Xiaofeng [1 ]
Li, Yingjie [1 ]
Tong, Kai [1 ]
机构
[1] Liaoyang Cent Hosp, Dept Anesthesiol, Liaoyang 111000, Peoples R China
来源
LATIN AMERICAN JOURNAL OF PHARMACY | 2019年 / 38卷 / 10期
关键词
cerebral ischemia-reperfusion; HO-1; inflammatory response; Nrf2; oxidative stress; sevoflurane; INFLAMMATORY RESPONSE; TNF-ALPHA; OXYGEN; APOPTOSIS; PROTECTS; PATHWAY; STRESS;
D O I
暂无
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
This study aimed to investigate the protective effect of sevoflurane postconditioning on cerebral ischemia-reperfusion (CIR) injury in rats and the mechanisms. Fifty-four male SD rats were randomly divided into sham-operated group, CIR group and CIR+sevoflurane postconditioning (CIR+SEV) group, 18 rats in each group. In CIR group and CIR+SPC group, the CIR model was established by ischemia for 120 min followed by reperfusion for 72 h. The CIR+SPC group received inhalation of sevoflurane with 1.0 time minimum alveolar concentration at the beginning of reperfusion, and the inhalation was continued for 30 min. Results showed that, after 72 h from ischemia, compared with CIR group, in CIR+SPC group the neurological deficit score was decreased, the brain water content and percentage of brain infarction area were decreased, the tumor necrosis factor-alpha and interleukin-1 beta levels were decreased, the brain tissue superoxide dismutase level was increased, the malondialdehyde and reactive oxygen species levels were decreased, and the brain tissue nuclear factor-erythroid 2 related factor 2 and heme oxygenase-1 protein expression levels were increased (all P < 0.05). Sevoflurane postconditioning can mitigate the brain injury in CIR in rats, which may be related to its resistance of inflammatory response and oxidative stress and regulation of nuclear factor-erythroid 2 related factor 2/heme oxygenase-1 signal pathway.
引用
收藏
页码:2001 / 2007
页数:7
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