Gokulan Kuppan, Karn Kumari, Sarkar Sumit, Raymick James, Khare Sangeeta
Division of Microbiology, National Center for Toxicological Research, US Food and Drug Administration, Jefferson, AR, USA.
Division of Neurotoxicology, National Center for Toxicological Research, US Food and Drug Administration, Jefferson, AR, USA.
J Alzheimers Dis Rep. 2025 Aug 12;9:25424823251358414. doi: 10.1177/25424823251358414. eCollection 2025 Jan-Dec.
High-fat diet (HFD) consumption is linked to Alzheimer's disease (AD). Identifying changes in the mRNA expression due to the ingestion of HFD in the intestine-often called the second brain due to its dense enteric neurons-could offer insights into AD development and progression.
This study assesses whether the introduction of HFD at adult-age influence expression of AD-related genes in the intestines of Wild-type (WT) or the amyloid precursor protein/presenilin1 (APP/PS1)-overexpressing Transgenic (TG) rats.
Twelve-month-old WT and TG rats (male and female) were fed a control diet (CD; 8% energy from fat), or HFD (45% energy from fat) for six months. Ileal tissues were assessed for the mRNA expression of genes responsible for development/progression of AD.
The WT HFD-fed rats (compared to CD-fed rats) showed increased mRNA expression of genes involved in the development of AD. In contrast, the TG HFD-fed female group, showed a higher number of upregulated genes compared to their respective CD-fed TG group. In TG HFD-fed rats there was higher mRNA expression of genes crucial for synaptic transmission such as in females and in males. Expression of was higher in HFD-fed TG female rats and HFD-fed WT male rats. Overall, the HFD-fed WT male showed mRNA expression of genes involved in the development of AD. However, HFD-fed TG females were more vulnerable for the progression of AD. It is likely that the enteric plays a major role in gut-brain axis for the development of AD in WT male, and progression of AD in TG female during the consumption of HFD.
The consumption of HFD perturbed the expression of enteric genes known to be involved in amyloid-β generation, clearance, and degradation, in a sex-dependent manner.
高脂饮食(HFD)的摄入与阿尔茨海默病(AD)有关。由于肠道中密集的肠神经元,其常被称为“第二大脑”,确定因摄入高脂饮食而导致的肠道中mRNA表达变化,可能有助于深入了解AD的发生和发展。
本研究评估成年期引入高脂饮食是否会影响野生型(WT)或过表达淀粉样前体蛋白/早老素1(APP/PS1)的转基因(TG)大鼠肠道中AD相关基因的表达。
给12个月大的WT和TG大鼠(雄性和雌性)喂食对照饮食(CD;脂肪提供8%的能量)或高脂饮食(HFD;脂肪提供45%的能量),持续6个月。评估回肠组织中负责AD发生/发展的基因的mRNA表达。
喂食高脂饮食的WT大鼠(与喂食对照饮食的大鼠相比)显示出参与AD发生的基因的mRNA表达增加。相比之下,喂食高脂饮食的TG雌性组与各自喂食对照饮食的TG组相比,上调基因的数量更多。在喂食高脂饮食的TG大鼠中,对突触传递至关重要的基因的mRNA表达更高,如雌性中的 和雄性中的 。 的表达在喂食高脂饮食的TG雌性大鼠和喂食高脂饮食的WT雄性大鼠中更高。总体而言,喂食高脂饮食的WT雄性大鼠显示出参与AD发生的基因的mRNA表达。然而,喂食高脂饮食的TG雌性大鼠在AD进展方面更易受影响。在食用高脂饮食期间,肠道 可能在WT雄性大鼠AD发生和TG雌性大鼠AD进展的肠-脑轴中起主要作用。
高脂饮食的摄入以性别依赖的方式扰乱了已知参与淀粉样β生成、清除和降解的肠道基因的表达。