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Gene Knockout of 5-Lipoxygenase Rescues Synaptic Dysfunction and Improves Memory in the Triple-Transgenic Model of Alzheimer’s Disease

机译:5脂氧合酶解救突触功能障碍的基因剔除并提高了内存在阿尔茨海默氏病的三转基因模型

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摘要

The 5-Lipoxygenase (5LO) is upregulated in Alzheimer’s disease (AD), and in vivo modulates the amyloidotic phenotype of APP transgenic mice. However, no data are available on the effects that 5LO has on synaptic function, integrity and cognition. To address this issue we used a genetic and a pharmacologic approach by generating 3xTg mice deficient for 5LO, and administering 3xTg mice which a 5LO inhibitor. Compared with controls, we found that even before the development of overt neuropathology, both animals manifested significant memory improvement, rescue of their synaptic dysfunction and amelioration of synaptic integrity. In addition, later in life these mice had a significant reduction of Aβ and tau pathology.Our findings support a novel functional role for 5LO in regulating synaptic plasticity and memory. They establish this proetin as a pleiotropic contributor to the development of the full spectrum of the AD phenotype, making it a valid therapeutic target for the treatment of AD.
机译:5-脂氧合酶(5LO)在阿尔茨海默氏病(AD)中被上调,并在体内调节APP转基因小鼠的淀粉样蛋白表型。但是,没有关于5LO对突触功能,完整性和认知的影响的数据。为了解决这个问题,我们使用遗传和药理学方法,生成了3xTg小鼠缺乏5LO的小鼠,并给予3xTg小鼠使用5LO抑制剂。与对照组相比,我们发现,即使在明显的神经病理学发展之前,两只动物都表现出明显的记忆力改善,突触功能障碍的缓解和突触完整性的改善。此外,这些小鼠在生命的后期具有Aβ和tau病理学的显着降低。我们的发现支持5LO在调节突触可塑性和记忆中的新功能。他们将这种蛋白质确定为促成AD表型全谱发展的多效贡献者,从而使其成为治疗AD的有效治疗靶标。

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