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Postictal behavioural impairments are due to a severe prolonged hypoperfusion/hypoxia event that is COX-2 dependent

机译:术后行为障碍是由于严重的长时间低灌注/缺氧事件所致而该事件取决于COX-2

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摘要

Seizures are often followed by sensory, cognitive or motor impairments during the postictal phase that show striking similarity to transient hypoxic/ischemic attacks. Here we show that seizures result in a severe hypoxic attack confined to the postictal period. We measured brain oxygenation in localized areas from freely-moving rodents and discovered a severe hypoxic event (pO2 < 10 mmHg) after the termination of seizures. This event lasted over an hour, is mediated by hypoperfusion, generalizes to people with epilepsy, and is attenuated by inhibiting cyclooxygenase-2 or L-type calcium channels. Using inhibitors of these targets we separated the seizure from the resulting severe hypoxia and show that structure specific postictal memory and behavioral impairments are the consequence of this severe hypoperfusion/hypoxic event. Thus, epilepsy is much more than a disease hallmarked by seizures, since the occurrence of postictal hypoperfusion/hypoxia results in a separate set of neurological consequences that are currently not being treated and are preventable.>DOI:
机译:发作后癫痫发作通常伴随感觉,认知或运动障碍,与短暂的缺氧/缺血发作表现出惊人的相似性。在这里,我们显示癫痫发作会导致严重的缺氧发作,并仅限于发作期。我们测量了自由活动的啮齿动物局部区域的大脑氧合作用,并在癫痫发​​作终止后发现了严重的缺氧事件(pO2 <10 mmHg)。该事件持续了一个多小时,由灌注不足介导,普遍存在于癫痫患者中,并通过抑制环氧合酶2或L型钙通道而减弱。使用这些靶标的抑制剂,我们将癫痫发作与造成的严重缺氧分开,并表明结构特异性的姿势记忆和行为障碍是这种严重的低灌注/缺氧事件的结果。因此,癫痫症不仅仅是癫痫发作的疾病,因为发作后的血流灌注不足/缺氧会导致另外一组神经系统后果,目前尚未得到治疗并且可以预防。> DOI:

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