Neuroglobin up-regulation after ischaemic pre-conditioning in a rat model of middle cerebral artery occlusion

被引:21
作者
Liu, Yichen [1 ,2 ]
Li, Baoquan [2 ]
Li, Qiaojun [1 ]
Zou, Liping [1 ]
机构
[1] Chinese PLA, Sch Med, Chinese PLA Gen Hosp, Dept Pediat, Beijing 100853, Peoples R China
[2] Chinese Peoples Liberat Army, Hosp 159, Dept Pediat, Zhumadian, Henan Province, Peoples R China
基金
中国国家自然科学基金;
关键词
Ischaemic pre-conditioning; middle cerebral artery occlusion; neuroglobin; neuroprotection; up-regulation; APOPTOTIC CELL-DEATH; VENTRICULAR-ARRHYTHMIAS; BRAIN; INJURY; MECHANISM; STROKE; DAMAGE;
D O I
10.3109/02699052.2014.1002004
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Primary objective: Neuroglobin (NGB) is a known neuroprotector and is up-regulated after ischaemia-hypoxia brain damage. However, no studies have investigated NGB levels after ischaemic pre-conditioning and middle cerebral artery occlusion (MCAO). Methods and procedures: This study subjected rats to different ischaemic pre-conditioning and MCAO regimens and assayed NGB levels in the hippocampus, cortex and hypothalamus by immunohistochemistry, quantitative polymerase chain reaction (PCR) and western blot. Main outcomes and results: After 30 minutes of ischaemic pre-conditioning, the number of NGB-positive cells and NGB levels in the hippocampus, cortex and hypothalamus were increased with longer reperfusion times, peaked at 24-hours reperfusion and slightly decreased at 48-hours reperfusion. Similarly, the mRNA and protein expression levels of NGB were also up-regulated; they peaked at 24-hours reperfusion and slightly decreased at 48-hours reperfusion. Conclusions: NGB may regulate neuroprotection against ischaemia and hypoxia-mediated brain damage after ischaemic pre-conditioning. The results provide additional evidence supporting the utility of ischaemic pre-conditioning and help elucidate its potential regulatory mechanism.
引用
收藏
页码:651 / 657
页数:7
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