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富集诱导CA1区NMDAR1基因敲除小鼠的结构变化并使其从非空间记忆缺陷中恢复。

Enrichment induces structural changes and recovery from nonspatial memory deficits in CA1 NMDAR1-knockout mice.

作者信息

Rampon C, Tang Y P, Goodhouse J, Shimizu E, Kyin M, Tsien J Z

机构信息

Department of Molecular Biology, Princeton University, Washington Road, Princeton, New Jersey 08540-1014, USA.

出版信息

Nat Neurosci. 2000 Mar;3(3):238-44. doi: 10.1038/72945.

Abstract

We produced CA1-specific NMDA receptor 1 subunit-knockout (CA1-KO) mice to determine the NMDA receptor dependence of nonspatial memory formation and of experience-induced structural plasticity in the CA1 region. CA1-KO mice were profoundly impaired in object recognition, olfactory discrimination and contextual fear memories. Surprisingly, these deficits could be rescued by enriching experience. Using stereological electron microscopy, we found that enrichment induced an increase of the synapse density in the CA1 region in knockouts as well as control littermates. Therefore, our data indicate that CA1 NMDA receptor activity is critical in hippocampus-dependent nonspatial memory, but is not essential for experience-induced synaptic structural changes.

摘要

我们培育了CA1区特异性N-甲基-D-天冬氨酸(NMDA)受体1亚基敲除(CA1-KO)小鼠,以确定CA1区非空间记忆形成和经验诱导的结构可塑性对NMDA受体的依赖性。CA1-KO小鼠在物体识别、嗅觉辨别和情境恐惧记忆方面存在严重缺陷。令人惊讶的是,这些缺陷可以通过丰富经验来挽救。使用体视学电子显微镜,我们发现丰富经验可诱导敲除小鼠以及对照同窝小鼠的CA1区突触密度增加。因此,我们的数据表明,CA1区NMDA受体活性在海马体依赖性非空间记忆中至关重要,但对于经验诱导的突触结构变化并非必不可少。

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