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ω-3对大鼠快速眼动睡眠剥夺所致认知缺陷的调节作用。

The role of omega-3 on modulation of cognitive deficiency induced by REM sleep deprivation in rats.

作者信息

Nasehi Mohammad, Mosavi-Nezhad Seyed-Moslem, Khakpai Fatemeh, Zarrindast Mohammad-Reza

机构信息

Cognitive and Neuroscience Reserch Center (CNRC), Tehran Medical Sciences Branch, Islamic Azad University, Tehran, Iran.

Department of Biology, Faculty of Basic Sciences, Science and Research Branch, Islamic Azad University, Tehran, Iran.

出版信息

Behav Brain Res. 2018 Oct 1;351:152-160. doi: 10.1016/j.bbr.2018.06.002. Epub 2018 Jun 2.

Abstract

Prolonged sleep deprivation causes cognitive deficits. In rats, for instance, sleep deprivation weakens spatial learning and long-term potentiation (LTP). We examined the effects of omega-3 on cognitive deficiency induced by REM sleep deprivation (RSD). For this purpose, we used a fear conditioning paradigm, forced swim test (FST) apparatus, and hot plate test. Intravenously omega-3 injection was performed during 3 consecutive days. Rats trained in the fear conditioning apparatus after 24 h. During conditioning, animals were received foot shocks, either alone or paired with a sound. Sleep deprivation paradigm was carried out in which REM sleep was completely prevented and non-REM sleep was intensely declined for 24 h. Then, context-dependent retention, anxiety behaviors, and hot plate tests were done. Auditory-dependent retention, anxiety behaviors, and FST were carried out 24 h later. 24 h of RSD impaired cognitive function, however intravenously administration of omega-3 improved (0.25, 0.5 and 1 mg/kg) context- or auditory-dependent memory, induced anxiolytic (1 mg/kg), antidepressant (1.25 mg/kg), and anti-nociceptive (0.25 mg/kg) effects. The results revealed that RSD interferes with the neural systems underlying cognitive functions and supports the involvement of omega-3 in the modulation of cognitive functions.

摘要

长期睡眠剥夺会导致认知缺陷。例如,在大鼠中,睡眠剥夺会削弱空间学习和长时程增强(LTP)。我们研究了ω-3对快速眼动睡眠剥夺(RSD)诱导的认知缺陷的影响。为此,我们使用了恐惧条件反射范式、强迫游泳试验(FST)装置和热板试验。连续3天进行静脉注射ω-3。24小时后在恐惧条件反射装置中训练大鼠。在条件反射过程中,动物接受单独或与声音配对的足部电击。进行睡眠剥夺范式,其中快速眼动睡眠被完全阻止,非快速眼动睡眠在24小时内急剧下降。然后,进行情境依赖性记忆保持、焦虑行为和热板试验。24小时后进行听觉依赖性记忆保持、焦虑行为和FST。24小时的RSD损害了认知功能,然而静脉注射ω-3(0.25、0.5和1mg/kg)改善了情境或听觉依赖性记忆,产生了抗焦虑(1mg/kg)、抗抑郁(1.25mg/kg)和抗伤害感受(0.25mg/kg)作用。结果表明,RSD干扰了认知功能背后的神经系统,并支持ω-3参与认知功能的调节。

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