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Regulation of microRNAs in high-fat diet induced hyperlipidemic hamsters
Dyslipidemia is a documented risk factor for cardiovascular diseases and other metabolic disorders. Therefore, the analysis of hyperlipidemia (HL)-related miRNAs is a potential approach for achieving new prognostic markers in lipid-metabolism related diseases. We aimed to analyze specific distributi...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7688633/ https://www.ncbi.nlm.nih.gov/pubmed/33239653 http://dx.doi.org/10.1038/s41598-020-77539-4 |
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author | Barbalata, Teodora Zhang, Lu Dulceanu, Madalina D. Stancu, Camelia S. Devaux, Yvan Sima, Anca V. Niculescu, Loredan S. |
author_facet | Barbalata, Teodora Zhang, Lu Dulceanu, Madalina D. Stancu, Camelia S. Devaux, Yvan Sima, Anca V. Niculescu, Loredan S. |
author_sort | Barbalata, Teodora |
collection | PubMed |
description | Dyslipidemia is a documented risk factor for cardiovascular diseases and other metabolic disorders. Therefore, the analysis of hyperlipidemia (HL)-related miRNAs is a potential approach for achieving new prognostic markers in lipid-metabolism related diseases. We aimed to analyze specific distribution of miRNAs in different tissues from HL animals. Golden Syrian hamsters were fed either regular chow (NL) or high-fat diet (HL) for 12 weeks. Microarray miRNAs profiling was performed in liver, heart and small intestine and data analyzed by R-studio software. Functional enrichment bioinformatics analysis was performed using miRWalk and DAVID tools. We observed a dysregulation of miRNAs in HL tissues evidencing a discrete distribution in the heart-liver axis and three lipid metabolism-related miRNAs were identified: hsa-miR-223-3p, hsa-miR-21-5p, and hsa-miR-146a-5p. Expression levels of these miRNAs were increased in HL livers and hearts. Functional bioinformatics analysis showed involvement of these miRNAs in the regulation of biological processes altered in HL conditions such as lipid metabolic process, fat cell differentiation, regulation of smooth muscle cells and cardiac septum development. We identified a set of miRNAs dysregulated in different tissues of HFD-induced HL hamsters. These findings motivate further studies aiming to investigate novel molecular mechanisms of lipid metabolism and atherogenic HL. |
format | Online Article Text |
id | pubmed-7688633 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-76886332020-11-27 Regulation of microRNAs in high-fat diet induced hyperlipidemic hamsters Barbalata, Teodora Zhang, Lu Dulceanu, Madalina D. Stancu, Camelia S. Devaux, Yvan Sima, Anca V. Niculescu, Loredan S. Sci Rep Article Dyslipidemia is a documented risk factor for cardiovascular diseases and other metabolic disorders. Therefore, the analysis of hyperlipidemia (HL)-related miRNAs is a potential approach for achieving new prognostic markers in lipid-metabolism related diseases. We aimed to analyze specific distribution of miRNAs in different tissues from HL animals. Golden Syrian hamsters were fed either regular chow (NL) or high-fat diet (HL) for 12 weeks. Microarray miRNAs profiling was performed in liver, heart and small intestine and data analyzed by R-studio software. Functional enrichment bioinformatics analysis was performed using miRWalk and DAVID tools. We observed a dysregulation of miRNAs in HL tissues evidencing a discrete distribution in the heart-liver axis and three lipid metabolism-related miRNAs were identified: hsa-miR-223-3p, hsa-miR-21-5p, and hsa-miR-146a-5p. Expression levels of these miRNAs were increased in HL livers and hearts. Functional bioinformatics analysis showed involvement of these miRNAs in the regulation of biological processes altered in HL conditions such as lipid metabolic process, fat cell differentiation, regulation of smooth muscle cells and cardiac septum development. We identified a set of miRNAs dysregulated in different tissues of HFD-induced HL hamsters. These findings motivate further studies aiming to investigate novel molecular mechanisms of lipid metabolism and atherogenic HL. Nature Publishing Group UK 2020-11-25 /pmc/articles/PMC7688633/ /pubmed/33239653 http://dx.doi.org/10.1038/s41598-020-77539-4 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Barbalata, Teodora Zhang, Lu Dulceanu, Madalina D. Stancu, Camelia S. Devaux, Yvan Sima, Anca V. Niculescu, Loredan S. Regulation of microRNAs in high-fat diet induced hyperlipidemic hamsters |
title | Regulation of microRNAs in high-fat diet induced hyperlipidemic hamsters |
title_full | Regulation of microRNAs in high-fat diet induced hyperlipidemic hamsters |
title_fullStr | Regulation of microRNAs in high-fat diet induced hyperlipidemic hamsters |
title_full_unstemmed | Regulation of microRNAs in high-fat diet induced hyperlipidemic hamsters |
title_short | Regulation of microRNAs in high-fat diet induced hyperlipidemic hamsters |
title_sort | regulation of micrornas in high-fat diet induced hyperlipidemic hamsters |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7688633/ https://www.ncbi.nlm.nih.gov/pubmed/33239653 http://dx.doi.org/10.1038/s41598-020-77539-4 |
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