Hippocampal proteomic changes in high-fat diet-induced obese mice associated with memory decline

被引:1
|
作者
Lu, Ping [1 ,2 ]
Gao, Cun-Xiu [1 ,2 ]
Luo, Fei-Jian [1 ,2 ]
Huang, Yu-Ting [1 ,2 ]
Gao, Mei-Mei [1 ,2 ]
Long, Yue-Sheng [1 ,2 ,3 ]
机构
[1] Guangzhou Med Univ, Affiliated Hosp 2, Inst Neurosci, Key Lab Neurogenet & Channelopathies Guangdong Pro, Guangzhou 510260, Peoples R China
[2] Guangzhou Med Univ, Affiliated Hosp 2, Minist Educ China, Guangzhou 510260, Peoples R China
[3] Changgang East Rd 250, Guangzhou 510260, Peoples R China
来源
基金
中国国家自然科学基金;
关键词
High fat diet; Memory decline; Obesity; Hippocampus; Postsynaptic density; Proteomic analysis; SYNAPTIC PLASTICITY; ALZHEIMERS-DISEASE; INSULIN-RESISTANCE; PROTEIN; MODEL; CONSEQUENCES; EXPRESSION; COMPLEXES; JUVENILE; KINASE;
D O I
10.1016/j.jnutbio.2023.109554
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Substantial evidence suggest that chronic consumption of high -fat diets (HFDs) can lead to obesity, abnormal metabolism, as well as cognitive impairment. Molecular and cellular changes regarding hippocampal dysfunctions have been identified in multiple HFD animal models. Therefore, in-depth identification of expression changes of hippocampal proteins is critical for understanding the mechanism of HFD-induced cognitive deficits. In this study, we fed 3-week-old male mice with HFD for 3 months to generate obese mice who exhibit systemic metabolic abnormality and learning and memory decline. Using an iTRAQ-labeled proteomic analysis, we identified a total of 82 differentially expressed proteins (DEPs) in the hippocampus upon HFD with 35 up-regulated proteins and 47 down-regulated proteins. Functional enrichment indicated that these DEPs were predominantly enriched in regulation of catabolic process, dendritic shaft, neuron projection morphogenesis and GTPase regulator activity. Protein -protein interaction enrichment showed that the DEPs are mostly enriched in postsynaptic functions; and of them, six proteins (i.e., DLG3, SYNGAP1, DCLK1, GRIA4, GRIP1, and ARHGAP32) were involved in several functional assemblies of the postsynaptic density including G-protein signaling, scaffolding and adaptor, kinase and AMPA signaling, respectively. Collectively, our findings suggest that these DEPs upon HFD might contribute to memory decline by disturbing neuronal and postsynaptic functions in the hippocampus. (c) 2023 Elsevier Inc. All rights reserved.
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页数:11
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