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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.
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页码:2001 / 2007
页数:7
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