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高脂肪饮食可诱导小鼠大脑胰岛素抵抗和认知障碍。

High fat diet induces brain insulin resistance and cognitive impairment in mice.

机构信息

Department of Nutrition, Dietetics, and Hospitality Management, Auburn University, Auburn, AL 36849, United States.

Department of Biology, Auburn University at Montgomery, AL 36124, United States.

出版信息

Biochim Biophys Acta Mol Basis Dis. 2017 Feb;1863(2):499-508. doi: 10.1016/j.bbadis.2016.10.006. Epub 2016 Oct 19.

Abstract

High fat diet-induced obesity is associated with insulin resistance (IR) and other chronic, diet related illnesses, including dementia. Alzheimer disease is the most common form of dementia, and is characterized by the presence of amyloid plaques and neurofibrillary tangles in brain. This study was designed to determine whether diet-induced changes in peripheral insulin sensitivity could contribute to alterations in brain insulin signaling and cognitive functions. Six week old, male C57BL/6NHsd mice were randomly assigned a high fat diet (40% energy from fat) with 42g/L liquid sugar (HFS) added to the drinking water or a normal chow diet (12% energy from fat) for 14weeks. Metabolic phenotypes were characterized for energy expenditure, physical activity, and food intake, and glucose and insulin tolerance tests. In addition, we examined the changes in protein expression related to brain insulin signaling and cognitive function. Mice fed HFS exhibited a statistically significant increase in obesity, and lower glucose and insulin tolerance as compared to animals fed the normal chow diet. In brain, HFS elicited IR as evidenced by a significant decrease in tyrosine phosphorylation of insulin receptor and an increase serine phosphorylation of IRS-1. These changes were accompanied by inflammatory (NFκB, JNK) and stress responses (p38 MAPK, CHOP) in whole brain lysate. In addition, HFS mouse brain exhibited biochemical changes related to increased amyloid beta deposition and neurofibrillary tangle formation, and decreased synaptic plasticity. These results suggested changes in insulin sensitivity might contribute to cognitive impairment associated with the HFS diet in mice.

摘要

高脂肪饮食诱导的肥胖与胰岛素抵抗(IR)和其他慢性、饮食相关疾病有关,包括痴呆症。阿尔茨海默病是最常见的痴呆症形式,其特征是大脑中存在淀粉样斑块和神经原纤维缠结。本研究旨在确定外周胰岛素敏感性的饮食变化是否会导致大脑胰岛素信号和认知功能的改变。将 6 周龄雄性 C57BL/6NHsd 小鼠随机分为高脂肪饮食组(脂肪提供 40%能量),饮用水中添加 42g/L 液体糖(HFS),或正常饲料饮食组(脂肪提供 12%能量),持续 14 周。对能量消耗、体力活动和食物摄入以及葡萄糖和胰岛素耐量试验进行了代谢表型特征分析。此外,我们还研究了与大脑胰岛素信号和认知功能相关的蛋白质表达变化。与正常饲料饮食喂养的动物相比,HFS 喂养的小鼠表现出明显的肥胖增加和葡萄糖及胰岛素耐量降低。在大脑中,HFS 引起 IR,表现为胰岛素受体酪氨酸磷酸化显著降低,IRS-1 丝氨酸磷酸化增加。这些变化伴随着全脑裂解物中炎症(NFκB、JNK)和应激反应(p38 MAPK、CHOP)的增加。此外,HFS 小鼠大脑表现出与淀粉样β沉积和神经原纤维缠结增加以及突触可塑性降低相关的生化变化。这些结果表明,胰岛素敏感性的变化可能导致 HFS 饮食与小鼠认知障碍有关。

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