单次缺氧事件可改善匹罗卡品诱导的涡虫高运动

Teagan Neufeld, Trevor N. Carniello, B. Dotta
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引用次数: 0

摘要

间歇性缺氧或缺氧治疗是在计划的或急性的时间框架内使个体暴露于低于大气水平的氧合条件下。缺氧治疗是一种潜在的新型治疗策略,可治疗多种疾病,包括线粒体疾病、运动训练和轻度认知障碍。线粒体功能障碍、多动运动和认知障碍是癫痫发作和癫痫持续状态(SE)的标志。癫痫发作可以被认为是大脑中不受控制的电活动,而癫痫发作是持续30分钟以上的癫痫发作,或者多次发作而在其间没有恢复意识。我们检验了使用匹罗卡品模型对棕涡虫(Dugesia tigrine)癫痫样活动的可能性。匹罗卡平是一种毒蕈碱类乙酰胆碱受体激动剂,能够造成癫痫相关的脑损伤。我们使用了5毫米剂量的匹罗卡品,然后测量了3分钟的空地行为。在整个测量阶段观察到运动性和厌恶性高运动。暴露于5 mM匹罗卡品后,涡虫表现出与癫痫发作一致的行为(例如,厌恶的多动运动和活动能力下降)。此外,我们测量了急性缺氧事件对涡虫行为的影响。我们用25%的碳酸水为涡虫创造一个低氧环境,然后测量3分钟的机动性和高动能运动。我们注意到暴露在低氧环境中不会产生行为变化。然而,当暴露于匹洛卡平后短暂(3分钟)缺氧发作时,由匹洛卡平引起的厌恶性多动运动完全不存在(p < 0.05)。当匹罗卡品的顺序和缺氧被平衡时,厌恶行为仍然存在。这种排序效应在40个试验中是一致的。进一步评估匹洛卡平癫痫发作模型和间歇性缺氧对涡虫行为的影响是必要的。
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A Single Hypoxic Event Ameliorates Pilocarpine Induced Hyperkinetic Movements in Planaria
Intermittent hypoxia or hypoxia therapy is exposing an individual to oxygenation conditions that are below atmospheric levels in a planned or acute timeframe. Hypoxia therapy is a potentially novel therapeutic strategy for a variety of pathologies including: mitochondrial disorders, exercise training, and mild cognitive impairments. Mitochondrial dysfunction, hyperkinetic movements, and cognitive impairments are hallmarks of seizures and status epilepticus (SE). A seizure can be considered uncontrolled electrical activity in the brain and SE is a seizure lasting more than 30 minutes, or multiple seizures without regaining con-sciousness in between. We examined the possibility of using the Pilocarpine model for seizure like activity on brown planaria (Dugesia tigrine). Pilocarpine is a muscarinic acetylcholine receptor agonist capable of creating seizure related brain damage. We utilized 5 mM dosages of pilocarpine and then measured open field behaviour for 3 minutes. Mobility and aversive hyperkinetic movements were observed throughout the measurement phase. After exposure to 5 mM pilocarpine, the planaria displayed behaviours consistent with seizures (e.g. aversive hyperkinetic movements and decreased mobility). Additionally, we measured the effects of an acute hypoxic event on Planaria behaviour. We used 25% carbonated water to create a hypoxic environment for the planaria and then measured mobility and hyperkinetic movements for 3 minutes. We noted that exposure to the hypoxic environment produced no changes in behaviour. However, the aversive hyperkinetic movements produced with pilocarpine administration were completely absent when a brief (3 minutes) hypoxic episode followed the pilocarpine exposure (p < 0.05). Aversive behaviours remained present when the ordering of pilocarpine and hypoxia were counterbalanced. This ordering effect was consistent across 40 trials. Further evaluation of the pilocarpine seizure model and intermittent hypoxia on planarian behaviour is warranted.
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