Effect of pre-condition cerebella fastigial nucleus electrical stimulation within and beyond the time window of thrombolytic on ischemic stroke in rats
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Effect of pre-condition cerebella fastigial nucleus electrical stimulation within and beyond the time window of thrombolytic on ischemic stroke in rats
Journal of Army Medical UniversityVol. 38, Issue 1, Pages: 27-31(2016)
Tang Weiju,Dong Weiwei,Xie Peng,Cheng Pengfei,Bai Shunjie,Ren Yifei,Wang Gong,Chen Xiuying,Cui Chun,Zhuang Yuxiang,Huang Wen.Effect of pre-condition cerebella fastigial nucleus electrical stimulation within and beyond the time window of thrombolytic on ischemic stroke in rats[J].J Amry Med Univ (J Third Mil Med Univ),2016,38(01):27-31.
Tang Weiju,Dong Weiwei,Xie Peng,Cheng Pengfei,Bai Shunjie,Ren Yifei,Wang Gong,Chen Xiuying,Cui Chun,Zhuang Yuxiang,Huang Wen.Effect of pre-condition cerebella fastigial nucleus electrical stimulation within and beyond the time window of thrombolytic on ischemic stroke in rats[J].J Amry Med Univ (J Third Mil Med Univ),2016,38(01):27-31.DOI:
Effect of pre-condition cerebella fastigial nucleus electrical stimulation within and beyond the time window of thrombolytic on ischemic stroke in rats
MPO)活性。 结果 FNS组能改善神经功能评分,PPARγ表达水平随溶栓再灌注时间呈逐渐增高的趋势,表达高峰可能在梗死后9 h前后,Western blot和RT-PCR检测结果均提示3、6、9、15 h FNS组与其对照组比较差异有统计学意义(P0.05);6、12 h和15 h FNS组脑梗死边缘区MPO活性与对照组比较差异有统计学意义(P0.05)。 结论 FNS对脑梗死大鼠有保护作用,并可适当延长大鼠局灶脑缺血溶栓时间窗,该作用可能与PPARγ介导的炎性调控作用有关。
Abstract
Objective To investigate the effect of neurogenic neuroprotection conferred by cerebellar fastigial nucleus stimulation (FNS) and the role of PPARγ-mediated inflammation in a rat model of cerebral ischemia reperfusion. Methods After a continuous 1-hour fastigial nucleus electric stimulation
the male Sprague-Dawley (SD) rats were immediately given middle cerebral artery occlusion (MCAO) for 1
3
6
9
12 and 15 h (n=5 for each time point) undergoing reperfusion with intravenous recombinant tissue plasminogen activator (rt-PA)
while the control group (n=30) received no FNS. After 72 h of reperfusion
the neurological deficits were evaluated. The brain tissue in ischemic penumbra was harvested to determine the myeloperoxidase (MPO) activity by a spectrophotometer
and the expression of PPARγ was measured by Western blotting and RT-PCR. Results FNS group had improved neurological deficits compared with the control group. The expression level of PPARγ was increased gradually with reperfusion time
and reached the peak after 9 hours’ reperfusion
and its mRNA and protein levels were obviously higher than each control group after 3
6
9
12 and 15 hours’ reperfusion (P0.05). The MPO activity was also significantly higher in 6
12 and 15 h after reperfusion in the FNS group than control group (P0.05). Conclusion FNS exerts neuroprotective effects and prolongs the therapeutic time window in rat cerebral ischemia/reperfusion
which might be related to the PPARγ-mediated inflammation in penumbral region.