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早年的前爪感觉运动剥夺会导致大鼠空间记忆和突触可塑性受损。

Forepaw sensorimotor deprivation in early life leads to the impairments on spatial memory and synaptic plasticity in rats.

作者信息

Zhang Yuanyuan, Li Fei, Cao Xiaohua, Jin Xingming, Yan Chonghuai, Tian Ying, Shen Xiaoming

机构信息

Shanghai Key Laboratory of Children's Environmental Health, Shanghai Institute for Pediatric Research, Xin Hua Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai 200092, China.

出版信息

J Biomed Biotechnol. 2009;2009:919276. doi: 10.1155/2009/919276. Epub 2010 Jan 4.

Abstract

To investigate the influence of forepaw sensorimotor deprivation on memory and synaptic plasticity, Sprague-Dawley rats were divided into two groups: a sham-operated group and a group deprived of forepaw sensorimotor function by microsurgical operation at postnatal day 13 (PN13). Behavioral and electrophysiological studies were performed at PN25, PN35, PN45, and PN60. Open field test was used to assess the spontaneous locomotor activity. Morris water maze was used to evaluate spatial reference learning and memory. The long-term potentiation (LTP) in the medial perforant path--dentate gyrus (MPP-DG) pathway was examined with hippocampal slices. We found that forepaw sensorimotor deprivation did not affect spontaneous activity of the rats. However, spatial reference learning and memory were significantly impaired in their early life (PN25, PN35, and PN45). In accordance with the behavior results, LTP in MPP-DG pathway was significantly suppressed in their early life. These data demonstrated that forepaw sensorimotor deprivation led to the impairments on spatial memory via inducing pronounced deficits in the MPP-DG pathway to exhibit LTP, one of the major cellular mechanisms underlying learning and memory.

摘要

为研究前爪感觉运动剥夺对记忆和突触可塑性的影响,将Sprague-Dawley大鼠分为两组:假手术组和在出生后第13天(PN13)通过显微手术剥夺前爪感觉运动功能的组。在PN25、PN35、PN45和PN60进行行为和电生理研究。采用旷场试验评估自发运动活动。采用莫里斯水迷宫评估空间参考学习和记忆。用海马脑片检测内侧穿通通路-齿状回(MPP-DG)通路的长时程增强(LTP)。我们发现前爪感觉运动剥夺不影响大鼠的自发活动。然而,它们在生命早期(PN25、PN35和PN45)的空间参考学习和记忆显著受损。与行为结果一致,MPP-DG通路的LTP在它们生命早期被显著抑制。这些数据表明,前爪感觉运动剥夺通过诱导MPP-DG通路出现明显缺陷以表现LTP(学习和记忆的主要细胞机制之一),从而导致空间记忆受损。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/33cd/2804797/cef66e2ae206/JBB2009-919276.001.jpg

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