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Srebf2 Locus Overexpression Reduces Body Weight, Total Cholesterol and Glucose Levels in Mice Fed with Two Different Diets

Macronutrients represent risk factors for hyperlipidemia or diabetes. Lipid alterations and type 2 diabetes mellitus are global health problems. Overexpression of sterol regulatory element-binding factor (Srebf2) in transgenic animals is linked to elevated cholesterol levels and diabetes development...

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Autores principales: Andrés-Blasco, Irene, Blesa, Sebastian, Vinué, Ángela, González-Navarro, Herminia, Real, José Tomás, Martínez-Hervás, Sergio, Carretero, Julián, Ferrández-Izquierdo, Antonio, Chaves, Felipe Javier, García-García, Ana-Bárbara
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7602228/
https://www.ncbi.nlm.nih.gov/pubmed/33066385
http://dx.doi.org/10.3390/nu12103130
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author Andrés-Blasco, Irene
Blesa, Sebastian
Vinué, Ángela
González-Navarro, Herminia
Real, José Tomás
Martínez-Hervás, Sergio
Carretero, Julián
Ferrández-Izquierdo, Antonio
Chaves, Felipe Javier
García-García, Ana-Bárbara
author_facet Andrés-Blasco, Irene
Blesa, Sebastian
Vinué, Ángela
González-Navarro, Herminia
Real, José Tomás
Martínez-Hervás, Sergio
Carretero, Julián
Ferrández-Izquierdo, Antonio
Chaves, Felipe Javier
García-García, Ana-Bárbara
author_sort Andrés-Blasco, Irene
collection PubMed
description Macronutrients represent risk factors for hyperlipidemia or diabetes. Lipid alterations and type 2 diabetes mellitus are global health problems. Overexpression of sterol regulatory element-binding factor (Srebf2) in transgenic animals is linked to elevated cholesterol levels and diabetes development. We investigated the impact of increased Srebf2 locus expression and the effects of control and high-fat, high-sucrose (HFHS) diets on body weight, glucose and lipid metabolisms in transgenic mice (S-mice). Wild type (WT) and S-mice were fed with both diets for 16 weeks. Plasma glucose, insulin and lipids were assessed (n = 25). Immunostainings were performed in liver, pancreas and fat (N = 10). Expression of Ldlr and Hmgcr in liver was performed by RT-PCR (N = 8). Control diet: S-mice showed reduced weight, insulin, total and HDL cholesterol and triglycerides (TG). HFHS diet widened differences in weight, total and HDL cholesterol, insulin and HOMA index but increased TG in S-mice. In S-mice, adipocyte size was lower while HFHS diet produced lower increase, pancreatic β-cell mass was lower with both diets and Srebf2, Ldlr and Hmgcr mRNA levels were higher while HFHS diet produced a rise in Srebf2 and Hmgcr levels. Srebf2 complete gene overexpression seems to have beneficial effects on metabolic parameters and to protect against HFHS diet effects.
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spelling pubmed-76022282020-11-01 Srebf2 Locus Overexpression Reduces Body Weight, Total Cholesterol and Glucose Levels in Mice Fed with Two Different Diets Andrés-Blasco, Irene Blesa, Sebastian Vinué, Ángela González-Navarro, Herminia Real, José Tomás Martínez-Hervás, Sergio Carretero, Julián Ferrández-Izquierdo, Antonio Chaves, Felipe Javier García-García, Ana-Bárbara Nutrients Article Macronutrients represent risk factors for hyperlipidemia or diabetes. Lipid alterations and type 2 diabetes mellitus are global health problems. Overexpression of sterol regulatory element-binding factor (Srebf2) in transgenic animals is linked to elevated cholesterol levels and diabetes development. We investigated the impact of increased Srebf2 locus expression and the effects of control and high-fat, high-sucrose (HFHS) diets on body weight, glucose and lipid metabolisms in transgenic mice (S-mice). Wild type (WT) and S-mice were fed with both diets for 16 weeks. Plasma glucose, insulin and lipids were assessed (n = 25). Immunostainings were performed in liver, pancreas and fat (N = 10). Expression of Ldlr and Hmgcr in liver was performed by RT-PCR (N = 8). Control diet: S-mice showed reduced weight, insulin, total and HDL cholesterol and triglycerides (TG). HFHS diet widened differences in weight, total and HDL cholesterol, insulin and HOMA index but increased TG in S-mice. In S-mice, adipocyte size was lower while HFHS diet produced lower increase, pancreatic β-cell mass was lower with both diets and Srebf2, Ldlr and Hmgcr mRNA levels were higher while HFHS diet produced a rise in Srebf2 and Hmgcr levels. Srebf2 complete gene overexpression seems to have beneficial effects on metabolic parameters and to protect against HFHS diet effects. MDPI 2020-10-14 /pmc/articles/PMC7602228/ /pubmed/33066385 http://dx.doi.org/10.3390/nu12103130 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Andrés-Blasco, Irene
Blesa, Sebastian
Vinué, Ángela
González-Navarro, Herminia
Real, José Tomás
Martínez-Hervás, Sergio
Carretero, Julián
Ferrández-Izquierdo, Antonio
Chaves, Felipe Javier
García-García, Ana-Bárbara
Srebf2 Locus Overexpression Reduces Body Weight, Total Cholesterol and Glucose Levels in Mice Fed with Two Different Diets
title Srebf2 Locus Overexpression Reduces Body Weight, Total Cholesterol and Glucose Levels in Mice Fed with Two Different Diets
title_full Srebf2 Locus Overexpression Reduces Body Weight, Total Cholesterol and Glucose Levels in Mice Fed with Two Different Diets
title_fullStr Srebf2 Locus Overexpression Reduces Body Weight, Total Cholesterol and Glucose Levels in Mice Fed with Two Different Diets
title_full_unstemmed Srebf2 Locus Overexpression Reduces Body Weight, Total Cholesterol and Glucose Levels in Mice Fed with Two Different Diets
title_short Srebf2 Locus Overexpression Reduces Body Weight, Total Cholesterol and Glucose Levels in Mice Fed with Two Different Diets
title_sort srebf2 locus overexpression reduces body weight, total cholesterol and glucose levels in mice fed with two different diets
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7602228/
https://www.ncbi.nlm.nih.gov/pubmed/33066385
http://dx.doi.org/10.3390/nu12103130
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