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阿尔茨海默病的载脂蛋白 E4 大鼠模型:性别差异、遗传风险和饮食。

APOE4 rat model of Alzheimer's disease: sex differences, genetic risk and diet.

机构信息

Center for Translational NeuroImaging, Northeastern University, Boston, MA, USA.

Department of Psychology, Northern Illinois University, DeKalb, IL, 60115, USA.

出版信息

BMC Neurosci. 2024 Nov 6;25(1):57. doi: 10.1186/s12868-024-00901-z.

Abstract

The strongest genetic risk factor for Alzheimer's disease (AD) is the ε4 allele of apolipoprotein E (ApoE ε4). A high fat diet also adds to the risk of dementia and AD. In addition, there are sex differences as women carriers have a higher risk of an earlier onset and rapid decline in memory than men. The present study looked at the effect of the genetic risk of ApoE ε4 together with a high fat/high sucrose diet (HFD/HSD) on brain function in male and female rats using magnetic resonance imaging. We hypothesized female carriers would present with deficits in cognitive behavior together with changes in functional connectivity as compared to male carriers. Four-month-old wildtype and human ApoE ε4 knock-in (TGRA8960), male and female Sprague Dawley rats were put on a HFD/HSD for four months. Afterwards they were imaged for changes in function using resting state BOLD functional connectivity. Images were registered to, and analyzed, using a 3D MRI rat atlas providing site-specific data on 173 different brain areas. Resting state functional connectivity showed male wildtype had greater connectivity between areas involved in feeding and metabolism while there were no differences between female and male carriers and wildtype females. The data were unexpected. The genetic risk was overshadowed by the diet. Male wildtype rats were most sensitive to the HFD/HSD presenting with a deficit in cognitive performance with enhanced functional connectivity in neural circuitry associated with food consumption and metabolism.

摘要

阿尔茨海默病(AD)最强的遗传风险因素是载脂蛋白 E(ApoE)ε4 等位基因(ApoE ε4)。高脂肪饮食也会增加痴呆和 AD 的风险。此外,还存在性别差异,女性携带者的发病年龄更早,记忆力下降更快。本研究使用磁共振成像,观察了 ApoE ε4 的遗传风险与高脂肪/高蔗糖饮食(HFD/HSD)一起对雄性和雌性大鼠大脑功能的影响。我们假设与雄性携带者相比,女性携带者的认知行为会出现缺陷,同时功能连接也会发生变化。将 4 个月大的野生型和人类 ApoE ε4 敲入(TGRA8960)雄性和雌性 Sprague Dawley 大鼠置于 HFD/HSD 中 4 个月。之后,使用静息状态 BOLD 功能连接对它们的功能变化进行成像。使用提供 173 个不同脑区的特定部位数据的 3D MRI 大鼠图谱对图像进行注册和分析。静息状态功能连接显示,雄性野生型大鼠在涉及进食和代谢的区域之间具有更大的连接性,而雌性和雄性携带者以及野生型雌性之间没有差异。数据出乎意料。遗传风险被饮食所掩盖。雄性野生型大鼠对 HFD/HSD 最为敏感,表现出认知表现的缺陷,与食物摄入和新陈代谢相关的神经回路的功能连接增强。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d08/11539573/ac611f2a5863/12868_2024_901_Fig1_HTML.jpg

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