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高脂肪饮食可保护阿尔茨海默病小鼠模型的血脑屏障。

High-fat diet protects the blood-brain barrier in an Alzheimer's disease mouse model.

机构信息

The Joseph Sagol Neuroscience Center, Sheba Medical Center, Tel Hashomer, Ramat Gan, Israel.

Gonda Brain Research Center, Bar Ilan University, Ramat-Gan, Israel.

出版信息

Aging Cell. 2018 Oct;17(5):e12818. doi: 10.1111/acel.12818. Epub 2018 Aug 6.

Abstract

Type 2 diabetes (T2D) is associated with increased risk of Alzheimer's disease (AD). There is evidence for impaired blood-brain barrier (BBB) in both diseases, but its role in the interplay between them is not clear. Here, we investigated the effects of high-fat diet (HFD), a model for T2D, on the Tg2576 mouse model of AD, in regard to BBB function. We showed that HFD mice had higher weight, more insulin resistance, and higher serum HDL cholesterol levels, primarily in Tg2576 mice, which also had higher brain lipids content. In terms of behavior, Tg2576 HFD mice were less active and more anxious, but had better learning in the Morris Water Maze compared to Tg2576 on regular diet. HFD had no effect on the level of amyloid beta 1-42 in the cortex of Tg2576 mice, but increased the transcription level of insulin receptor in the hippocampus. Tg2576 mice on regular diet demonstrated more BBB disruption at 8 and 12 months accompanied by larger lateral ventricles volume in contrast to Tg2576 HFD mice, whose BBB leakage and ventricular volume were similar to wild-type (WT) mice. Our results suggest that in AD, HFD may promote better cognitive function through improvements of BBB function and of brain atrophy but not of amyloid beta levels. Lipid metabolism in the CNS and peripheral tissues and brain insulin signaling may underlie this protection.

摘要

2 型糖尿病(T2D)与阿尔茨海默病(AD)的风险增加有关。这两种疾病都有证据表明血脑屏障(BBB)受损,但它在它们之间相互作用中的作用尚不清楚。在这里,我们研究了高脂肪饮食(HFD),即 T2D 的模型,对 AD 的 Tg2576 小鼠模型的影响,主要是针对 BBB 功能。我们发现 HFD 小鼠体重增加、胰岛素抵抗更严重、血清高密度脂蛋白胆固醇水平更高,尤其是在 Tg2576 小鼠中,其大脑脂质含量也更高。在行为方面,Tg2576 HFD 小鼠的活动量较少且更焦虑,但与 Tg2576 正常饮食组相比,在 Morris 水迷宫中的学习能力更好。HFD 对 Tg2576 皮质中的淀粉样β 1-42 水平没有影响,但增加了海马中的胰岛素受体转录水平。与 Tg2576 HFD 小鼠相比,正常饮食的 Tg2576 小鼠在 8 个月和 12 个月时 BBB 破坏更严重,伴随侧脑室体积增大,而 Tg2576 HFD 小鼠的 BBB 渗漏和脑室体积与野生型(WT)小鼠相似。我们的结果表明,在 AD 中,HFD 可能通过改善 BBB 功能和脑萎缩来促进更好的认知功能,但不能改善淀粉样β水平。中枢神经系统和外周组织的脂质代谢以及大脑胰岛素信号可能是这种保护的基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7865/6156545/41d34031f91d/ACEL-17-e12818-g001.jpg

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