The neuroprotective role of prolonged normobaric oxygenation applied during ischemia and in the early stage of reperfusion in cerebral ischemic rats

被引:2
|
作者
Gao, Daiquan [1 ]
Yuan, Shuhua [1 ]
Ji, Xunming [2 ]
Su, Yingying [3 ]
Qi, Zhifeng [1 ]
机构
[1] Capital Med Univ, Cerebrovascular Dis Res Inst, Dept Neurol, Xuanwu Hosp, Beijing, Peoples R China
[2] Capital Med Univ, Beijing Inst Brain Disorders, Ctr Stroke, Beijing, Peoples R China
[3] Capital Med Univ, Dept Neurol, Xuanwu Hosp, Beijing, Peoples R China
关键词
Prolonged normobaric oxygenation; Neuroprotection; Apoptosis; Matrix metalloproteinase-2 (MMP-2) nitro-; sylation; Poly(ADP-ribose)polymerase-1 (PARP-1); Stroke; Recanalization; Cerebral ischemia; PLASMINOGEN-ACTIVATOR TREATMENT; BRAIN; GENE;
D O I
10.1016/j.brainres.2023.148464
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Background: Recanalization is the main treatment option for ischemic stroke. However, prognosis remains poor for about half of patients after recanalization, possibly due to the "no-reflow" phenomenon at the early phase of recanalization. Normobaric oxygenation (NBO) during ischemia can reportedly maintain the partial pressure of oxygen and exert a protective effect in ischemic brain tissue.Objectives and methods: This study investigated whether prolonged NBO treatment during ischemia and the early phase of reperfusion (i/rNBO) has neuroprotective effects and to elucidate the underlying mechanisms in rats with middle cerebral artery occlusion plus reperfusion.Results: NBO treatment significantly elevated the level of O2 in the atmosphere and arterial blood without altering the level of CO2. The infarcted cerebral volume was significantly reduced by application of i/rNBO as compared to iNBO (applied during ischemia) or rNBO (applied at the early phase of reperfusion), indicating better protective effects of i/rNBO. i/rNBO more effectively suppressed s-nitrosylation of MMP-2 (amplifying inflammation) as compared to iNBO and rNBO, dramatically downregulated the cleavage of poly(ADP-ribose) polymerase-1 (PARP-1, acting as the substrate of MMP-2), and suppressed neuronal apoptosis, as determined by the TUNEL assay and staining for NeuN. These results demonstrated that application of i/rNBO in the early stage of reperfusion significantly alleviated neuronal apoptosis via suppression of the MMP-2/PARP-1 pathway.Conclusions: The mechanism underlying the neuroprotective role of i/rNBO involved prolonged NBO treatment for cerebral ischemia, suggesting that i/rNBO may allow expansion of the time window for NBO application in stroke patients following vascular recanalization.
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页数:6
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