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Differential proteomic analysis of mouse cerebrums with high-fat diet (HFD)-induced hyperlipidemia

Hyperlipidemia is a chronic disease characterized by elevated blood cholesterol and triglycerides and there is accumulated evidence that the disease might affect brain functions. Here we report on a proteomic analysis of the brain proteins in hyperlipidemic mice. Hyperlipidemia was successfully indu...

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Autores principales: Chen, Changming, Wen, Meiling, Wang, Caixia, Yuan, Zhongwen, Jin, Ya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PeerJ Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9356585/
https://www.ncbi.nlm.nih.gov/pubmed/35942128
http://dx.doi.org/10.7717/peerj.13806
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author Chen, Changming
Wen, Meiling
Wang, Caixia
Yuan, Zhongwen
Jin, Ya
author_facet Chen, Changming
Wen, Meiling
Wang, Caixia
Yuan, Zhongwen
Jin, Ya
author_sort Chen, Changming
collection PubMed
description Hyperlipidemia is a chronic disease characterized by elevated blood cholesterol and triglycerides and there is accumulated evidence that the disease might affect brain functions. Here we report on a proteomic analysis of the brain proteins in hyperlipidemic mice. Hyperlipidemia was successfully induced in mice by a 20 week high-fat diet (HFD) feeding (model group). A control group with a normal diet and a treatment group with HFD-fed mice treated with a lipid-lowering drug simvastatin (SIM) were established accordingly. The proteins were extracted from the left and right cerebrum hemispheres of the mice in the three groups and subjected to shotgun proteomic analysis. A total of 4,422 proteins were detected in at least half of the samples, among which 324 proteins showed significant difference (fold change >1.5 or <0.67, p < 0.05) in at least one of the four types of comparisons (left cerebrum hemispheres of the model group versus the control group, right cerebrums of model versus control, left cerebrums of SIM versus model, right cerebrums of SIM versus model). Biological process analysis revealed many of these proteins were enriched in the processes correlated with lipid metabolism, neurological disorders, synaptic events and nervous system development. For the first time, it has been reported that some of the proteins have been altered in the brain under the conditions of HFD feeding, obesity or hyperlipidemia. Further, 22 brain processes-related proteins showed different expression in the two cerebrum hemispheres, suggesting changes of the brain proteins caused by hyperlipidemia might also be asymmetric. We hope this work will provide useful information to understand the effects of HFD and hyperlipidemia on brain proteins.
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spelling pubmed-93565852022-08-07 Differential proteomic analysis of mouse cerebrums with high-fat diet (HFD)-induced hyperlipidemia Chen, Changming Wen, Meiling Wang, Caixia Yuan, Zhongwen Jin, Ya PeerJ Biochemistry Hyperlipidemia is a chronic disease characterized by elevated blood cholesterol and triglycerides and there is accumulated evidence that the disease might affect brain functions. Here we report on a proteomic analysis of the brain proteins in hyperlipidemic mice. Hyperlipidemia was successfully induced in mice by a 20 week high-fat diet (HFD) feeding (model group). A control group with a normal diet and a treatment group with HFD-fed mice treated with a lipid-lowering drug simvastatin (SIM) were established accordingly. The proteins were extracted from the left and right cerebrum hemispheres of the mice in the three groups and subjected to shotgun proteomic analysis. A total of 4,422 proteins were detected in at least half of the samples, among which 324 proteins showed significant difference (fold change >1.5 or <0.67, p < 0.05) in at least one of the four types of comparisons (left cerebrum hemispheres of the model group versus the control group, right cerebrums of model versus control, left cerebrums of SIM versus model, right cerebrums of SIM versus model). Biological process analysis revealed many of these proteins were enriched in the processes correlated with lipid metabolism, neurological disorders, synaptic events and nervous system development. For the first time, it has been reported that some of the proteins have been altered in the brain under the conditions of HFD feeding, obesity or hyperlipidemia. Further, 22 brain processes-related proteins showed different expression in the two cerebrum hemispheres, suggesting changes of the brain proteins caused by hyperlipidemia might also be asymmetric. We hope this work will provide useful information to understand the effects of HFD and hyperlipidemia on brain proteins. PeerJ Inc. 2022-08-03 /pmc/articles/PMC9356585/ /pubmed/35942128 http://dx.doi.org/10.7717/peerj.13806 Text en ©2022 Chen et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ) and either DOI or URL of the article must be cited.
spellingShingle Biochemistry
Chen, Changming
Wen, Meiling
Wang, Caixia
Yuan, Zhongwen
Jin, Ya
Differential proteomic analysis of mouse cerebrums with high-fat diet (HFD)-induced hyperlipidemia
title Differential proteomic analysis of mouse cerebrums with high-fat diet (HFD)-induced hyperlipidemia
title_full Differential proteomic analysis of mouse cerebrums with high-fat diet (HFD)-induced hyperlipidemia
title_fullStr Differential proteomic analysis of mouse cerebrums with high-fat diet (HFD)-induced hyperlipidemia
title_full_unstemmed Differential proteomic analysis of mouse cerebrums with high-fat diet (HFD)-induced hyperlipidemia
title_short Differential proteomic analysis of mouse cerebrums with high-fat diet (HFD)-induced hyperlipidemia
title_sort differential proteomic analysis of mouse cerebrums with high-fat diet (hfd)-induced hyperlipidemia
topic Biochemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9356585/
https://www.ncbi.nlm.nih.gov/pubmed/35942128
http://dx.doi.org/10.7717/peerj.13806
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