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首页> 外文期刊>The Journal of Neuroscience: The Official Journal of the Society for Neuroscience >Environmental enrichment restores memory functioning in mice with impaired IL-1 signaling via reinstatement of long-term potentiation and spine size enlargement.
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Environmental enrichment restores memory functioning in mice with impaired IL-1 signaling via reinstatement of long-term potentiation and spine size enlargement.

机译:通过恢复长期增强能力和脊柱尺寸扩大,环境富集可恢复IL-1信号受损的小鼠的记忆功能。

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摘要

Environmental enrichment (EE) was found to facilitate memory functioning and neural plasticity in normal and neurologically impaired animals. However, the ability of this manipulation to rescue memory and its biological substrate in animals with specific genetically based deficits in these functions has not been extensively studied. In the present study, we investigated the effects of EE in two mouse models of impaired memory functioning and plasticity. Previous research demonstrated that mice with a deletion of the receptor for the cytokine interleukin-1 (IL-1rKO), and mice with CNS-specific transgenic over-expression of the IL-1 receptor antagonist (IL-1raTG) display impaired hippocampal memory and long-term potentiation (LTP). We report here a corrective effect of EE on spatial and contextual memory in IL-1rKO and IL-1raTG mice and reveal two mechanisms for this beneficial effect: Concomitantly with their disturbed memory functioning, LTP in IL-1rKO mice that were raised in a regular environment is impaired, and their dendritic spine size is reduced. Both of these impairments were corrected by environmental enrichment. No deficiencies in neurogenesis or hippocampal BDNF and vascular endothelial growth factor secretion were found in IL-1rKO mice that were raised in a regular environment, and both of these variables were increased to a similar degree in enriched IL-1rKO and wild-type mice. These findings suggest that exposure to an enriched environment may be beneficial for individuals with impaired learning and memory related to genetic impairments of IL-1 signaling (and possibly other genetic causes), by reversing impairments in dentate gyrus LTP and spine size and by promoting neurogenesis and trophic factors secretion.
机译:发现环境富集(EE)有助于正常和神经系统受损动物的记忆功能和神经可塑性。但是,这种操作在具有特定遗传缺陷的动物中拯救记忆及其生物底物的能力尚未得到广泛研究。在本研究中,我们调查了记忆功能和可塑性受损的两个小鼠模型中EE的影响。先前的研究表明,缺失细胞因子白介素1(IL-1rKO)的小鼠和具有中枢神经系统特异性转基因IL-1受体拮抗剂(IL-1raTG)的小鼠表现出受损的海马记忆和长期增强(LTP)。我们在这里报告EE对IL-1rKO和IL-1raTG小鼠的空间和背景记忆的纠正作用,并揭示了这种有益作用的两种机制:伴随其记忆功能的紊乱,IL-1rKO小鼠中的LTP定期升高环境受损,树突棘尺寸减小。这些损害都通过环境富集得到纠正。在正常环境中饲养的IL-1rKO小鼠中未发现神经发生或海马BDNF和血管内皮生长因子分泌不足,并且在富集的IL-1rKO和野生型小鼠中,这两个变量均以相似的程度增加。这些发现表明,通过逆转齿状回LTP和脊柱大小的损伤并促进神经发生,暴露于丰富的环境可能有益于与IL-1信号遗传损伤(可能还有其他遗传原因)相关的学习和记忆障碍的个体。和营养因子的分泌。

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