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短期和长期饮食性高血糖对肝脏和视网膜代谢途径的选择性转录组失调。

Selective transcriptomic dysregulation of metabolic pathways in liver and retina by short- and long-term dietary hyperglycemia.

作者信息

Mondal Anupam K, Brock Daniel C, Rowan Sheldon, Yang Zhi-Hong, Rojulpote Krishna Vamsi, Smith Kelsey M, Francisco Sarah G, Bejarano Eloy, English Milton A, Deik Amy, Jeanfavre Sarah, Clish Clary B, Remaley Alan T, Taylor Allen, Swaroop Anand

机构信息

Neurobiology Neurodegeneration & Repair Laboratory, National Eye Institute (NEI), National Institutes of Health (NIH), Bethesda, MD, USA.

Laboratory for Nutrition & Vision Research, JM-USDA Human Nutrition Research Center on Aging, Tufts University, Boston, MA, USA.

出版信息

iScience. 2024 Jan 19;27(2):108979. doi: 10.1016/j.isci.2024.108979. eCollection 2024 Feb 16.

Abstract

A high glycemic index (HGI) diet induces hyperglycemia, a risk factor for diseases affecting multiple organ systems. Here, we evaluated tissue-specific adaptations in the liver and retina after feeding HGI diet to mice for 1 or 12 month. In the liver, genes associated with inflammation and fatty acid metabolism were altered within 1 month of HGI diet, whereas 12-month HGI diet-fed group showed dysregulated expression of cytochrome P450 genes and overexpression of lipogenic factors including and . In contrast, retinal transcriptome exhibited HGI-related notable alterations in energy metabolism genes only after 12 months. Liver fatty acid profiles in HGI group revealed higher levels of monounsaturated and lower levels of saturated and polyunsaturated fatty acids. Additionally, HGI diet increased blood low-density lipoprotein, and diet-aging interactions affected expression of mitochondrial oxidative phosphorylation genes in the liver and disease-associated genes in retina. Thus, our findings provide new insights into retinal and hepatic adaptive mechanisms to dietary hyperglycemia.

摘要

高血糖指数(HGI)饮食会引发高血糖,而高血糖是影响多个器官系统的疾病的一个风险因素。在此,我们评估了给小鼠喂食HGI饮食1个月或12个月后肝脏和视网膜的组织特异性适应性变化。在肝脏中,与炎症和脂肪酸代谢相关的基因在喂食HGI饮食1个月内就发生了改变,而喂食12个月HGI饮食的组显示细胞色素P450基因表达失调,包括……等生脂因子过度表达。相比之下,视网膜转录组仅在12个月后才在能量代谢基因方面表现出与HGI相关的显著变化。HGI组的肝脏脂肪酸谱显示单不饱和脂肪酸水平较高,饱和脂肪酸和多不饱和脂肪酸水平较低。此外,HGI饮食会增加血液中的低密度脂蛋白,饮食与衰老的相互作用会影响肝脏中线粒体氧化磷酸化基因以及视网膜中疾病相关基因的表达。因此,我们的研究结果为视网膜和肝脏对饮食性高血糖的适应性机制提供了新的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d94a/10850775/f28866d6c790/fx1.jpg

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