高原环境对睡眠剥夺大鼠行为学及海马CA1区超微结构的影响

目的探讨高原环境对睡眠剥夺大鼠学习记忆能力和海马CAl区超微结构的影响。方法采用小平台水环境法建立大鼠睡眠剥夺模型,并随机分为兰州组(海拔1520m)和可可西里组(海拔4767m);Morris水迷宫实验评价不同高原环境对大鼠空间分辨学习能力的影响,透射电子显微镜观察其海马CAl区超微结构变化。结果与兰州组相比,可可西里组大鼠随着睡眠剥夺时间的延长,呈现兴奋-激惹-抑制变化,但程度逐渐减弱且低头思睡时间明显增多;超微结构观察海马CAl区神经元胞体明显肿胀,核膜消失,胞核缩小,细胞器数目减少,微血管周围胶质足板肿胀、破裂,典型突触结构消失。睡眠剥夺第1,3和5天,可可西里组大鼠逃避潜伏期延长(均...

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Published in中国现代神经疾病杂志 Vol. 14; no. 4; pp. 329 - 334
Main Author 司江华 彭小兰 杨金升 严雯 谢守嫔 赵静
Format Journal Article
LanguageChinese
Published 730050,甘肃省兰州市第一人民医院神经内科%730070,兰州军区兰州总医院神经内科 2014
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ISSN1672-6731
DOI10.3969/j.issn.1672-6731.2014.04.012

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Summary:目的探讨高原环境对睡眠剥夺大鼠学习记忆能力和海马CAl区超微结构的影响。方法采用小平台水环境法建立大鼠睡眠剥夺模型,并随机分为兰州组(海拔1520m)和可可西里组(海拔4767m);Morris水迷宫实验评价不同高原环境对大鼠空间分辨学习能力的影响,透射电子显微镜观察其海马CAl区超微结构变化。结果与兰州组相比,可可西里组大鼠随着睡眠剥夺时间的延长,呈现兴奋-激惹-抑制变化,但程度逐渐减弱且低头思睡时间明显增多;超微结构观察海马CAl区神经元胞体明显肿胀,核膜消失,胞核缩小,细胞器数目减少,微血管周围胶质足板肿胀、破裂,典型突触结构消失。睡眠剥夺第1,3和5天,可可西里组大鼠逃避潜伏期延长(均P〈O.05)、游泳路程增加(均P〈0.05),而穿越平台次数减少(均P〈0.05)。结论高原环境可使睡眠剥夺大鼠学习记忆能力进一步降低,其机制可能与海马CAl区超微结构变化有关。
Bibliography:Altitude; Sleep deprivation; Memory disorders; Maze learning; Hippocampus; Synapses; Microscopy, electron, transmission; Disease models, animal
Objective To investigate the effects of high-altitude environment on cognitive function and uhrastructure in CA1 region of the hippocampus of Wistar rats in sleep deprivation (SD). Methods SD was induced in Wistar rats by employing "flower pot" technique. Sixty-four rats were randomly divided into 2 groups: Lanzhou group (at an altitude of 1520 m) and Kekexili group (at an altitude of 4767 m), and each group was further divided into 4 subgroups according to the time of SD (0, 1, 3 and 5 d). The behaviors of rats were studied by Morris. water maze test at given time points. The ultrastructure of hippocampal neurons was observed by transmission electron microscope (TEM). Results 1) Compared with Lanzhou group, rat behavior of Kekexili group presented excitement-irritation-suppression changes with the extension of SD time, but the extent was weakened gradually, and time o
ISSN:1672-6731
DOI:10.3969/j.issn.1672-6731.2014.04.012