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胞外核苷酸焦磷酸酶磷酸二酯酶-1的过表达会增强与高脂饮食和胰岛素抵抗相关的认知缺陷。

Cognitive deficits associated with a high-fat diet and insulin resistance are potentiated by overexpression of ecto-nucleotide pyrophosphatase phosphodiesterase-1.

作者信息

Kasper J M, Milton A J, Smith A E, Laezza F, Taglialatela G, Hommel J D, Abate N

机构信息

Center for Addiction Research, Department of Pharmacology and Toxicology, University of Texas Medical Branch, Galveston, TX, United States.

Center for Addiction Research, Department of Pharmacology and Toxicology, University of Texas Medical Branch, Galveston, TX, United States.

出版信息

Int J Dev Neurosci. 2018 Feb;64:48-53. doi: 10.1016/j.ijdevneu.2017.03.011. Epub 2017 Mar 31.

Abstract

There is growing evidence that over consumption of high-fat foods and insulin resistance may alter hippocampal-dependent cognitive function. To study the individual contributions of diet and peripheral insulin resistance to learning and memory, we used a transgenic mouse line that overexpresses ecto-nucleotide pyrophosphatase phosphodiesterase-1 in adipocytes, which inhibits the insulin receptor. Here, we demonstrate that a model of peripheral insulin resistance exacerbates high-fat diet induced deficits in performance on the Morris Water Maze task. This finding was then reviewed in the context of the greater literature to explore potential mechanisms including triglyceride storage, adiponectin, lipid composition, insulin signaling, oxidative stress, and hippocampal signaling. Together, these findings further our understanding of the complex relationship among peripheral insulin resistance, diet and memory.

摘要

越来越多的证据表明,高脂肪食物的过度摄入和胰岛素抵抗可能会改变海马体依赖的认知功能。为了研究饮食和外周胰岛素抵抗对学习和记忆的个体影响,我们使用了一种转基因小鼠品系,该品系在脂肪细胞中过表达胞外核苷酸焦磷酸酶磷酸二酯酶-1,其可抑制胰岛素受体。在此,我们证明外周胰岛素抵抗模型会加剧高脂饮食诱导的莫里斯水迷宫任务表现缺陷。然后,我们结合更多文献对这一发现进行了综述,以探索潜在机制,包括甘油三酯储存、脂联素、脂质组成、胰岛素信号传导、氧化应激和海马体信号传导。这些发现共同加深了我们对外周胰岛素抵抗、饮食和记忆之间复杂关系的理解。

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