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Limited Therapeutic Time Windows of Mild-to-Moderate Hypothermia in a Focal Ischemia Model in Rat

机译:大鼠局灶性缺血模型中轻度至中度低温的治疗时间窗有限

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摘要

Although many studies have shown the great potential of induced hypothermia in stroke treatment, we recognize that there are limitations to the protective effects of hypothermia even in the laboratory. Here, we review our experiments on the protective effects of mild-to-moderate hypothermia in rats. Focal ischemia was induced by bilateral common carotid artery (CCA) occlusion for 1 to 2 hours combined with permanent or transient middle cerebral artery (MCA) occlusion. We compared the effects of mild (33°C) and moderate (30°C) hypothermia, evaluated therapeutic time windows, and studied the underlying mechanisms. On review, our findings revealed that the protective effects of induced mild hypothermia (33°C) were limited, and the therapeutic time window of even moderate hypothermia (30°C) was very short in our specific models, although this limitation might be due to the relatively brief periods of hypothermia used. In addition, we found that hypothermia reduced brain injury by preserving Akt activity, PTEN phosphorylation and εPKC activity, while inhibiting ROS production, and δPKC activity.
机译:尽管许多研究表明诱发体温过低在中风治疗中具有巨大潜力,但我们认识到即使在实验室中,体温过低的保护作用也存在局限性。在这里,我们回顾我们的实验对轻度至中度低温对大鼠的保护作用。局灶性缺血是由双侧颈总动脉(CCA)阻塞1到2小时,并伴有永久性或短暂性大脑中动脉(MCA)阻塞所致。我们比较了轻度(33°C)和中度(30°C)体温过低的影响,评估了治疗时间窗,并研究了潜在的机制。经审查,我们的发现表明,在我们的特定模型中,诱导性亚低温(33°C)的保护作用是有限的,即使是中度亚低温(30°C)的治疗时间窗口也很短,尽管这种局限可能是由于相对较短的低温疗程。此外,我们发现低温可以通过保留Akt活性,PTEN磷酸化和εPKC活性,同时抑制ROS产生和δPKC活性来减少脑损伤。

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