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A Comparative Study of the Metabolic and Skeletal Response of C57BL/6J and C57BL/6N Mice in a Diet-Induced Model of Type 2 Diabetes

Type 2 diabetes mellitus (T2DM) represents a complex clinical scenario of altered energy metabolism and increased fracture incidence. The C57BL/6 mouse model of diet-induced obesity has been used to study the mechanisms by which altered glucose homeostasis affects bone mass and quality, but genetic...

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Autores principales: Rendina-Ruedy, Elizabeth, Hembree, Kelsey D., Sasaki, Angela, Davis, McKale R., Lightfoot, Stan A., Clarke, Stephen L., Lucas, Edralin A., Smith, Brenda J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4469802/
https://www.ncbi.nlm.nih.gov/pubmed/26146567
http://dx.doi.org/10.1155/2015/758080
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author Rendina-Ruedy, Elizabeth
Hembree, Kelsey D.
Sasaki, Angela
Davis, McKale R.
Lightfoot, Stan A.
Clarke, Stephen L.
Lucas, Edralin A.
Smith, Brenda J.
author_facet Rendina-Ruedy, Elizabeth
Hembree, Kelsey D.
Sasaki, Angela
Davis, McKale R.
Lightfoot, Stan A.
Clarke, Stephen L.
Lucas, Edralin A.
Smith, Brenda J.
author_sort Rendina-Ruedy, Elizabeth
collection PubMed
description Type 2 diabetes mellitus (T2DM) represents a complex clinical scenario of altered energy metabolism and increased fracture incidence. The C57BL/6 mouse model of diet-induced obesity has been used to study the mechanisms by which altered glucose homeostasis affects bone mass and quality, but genetic variations in substrains of C57BL/6 may have confounded data interpretation. This study investigated the long-term metabolic and skeletal consequences of two commonly used C57BL/6 substrains to a high fat (HF) diet. Male C57BL/6J, C57BL/6N, and the negative control strain, C3H/HeJ, mice were fed a control or HF diet for 24 wks. C57BL/6N mice on a HF diet demonstrated an increase in plasma insulin and blood glucose as early as 4 wk, whereas these responses were delayed in the C57BL/6J mice. The C57BL/6N mice exhibited more severe hepatic steatosis and inflammation. Only the C57BL/6N mice lost significant trabecular bone in response to the high fat diet. The C3H/HeJ mice were protected from bone loss. The data show that C57BL/6J and C57BL/6N mice differ in their metabolic and skeletal response when fed a HF diet. These substrain differences should be considered when designing experiments and are likely to have implications on data interpretation and reproducibility.
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spelling pubmed-44698022015-07-05 A Comparative Study of the Metabolic and Skeletal Response of C57BL/6J and C57BL/6N Mice in a Diet-Induced Model of Type 2 Diabetes Rendina-Ruedy, Elizabeth Hembree, Kelsey D. Sasaki, Angela Davis, McKale R. Lightfoot, Stan A. Clarke, Stephen L. Lucas, Edralin A. Smith, Brenda J. J Nutr Metab Research Article Type 2 diabetes mellitus (T2DM) represents a complex clinical scenario of altered energy metabolism and increased fracture incidence. The C57BL/6 mouse model of diet-induced obesity has been used to study the mechanisms by which altered glucose homeostasis affects bone mass and quality, but genetic variations in substrains of C57BL/6 may have confounded data interpretation. This study investigated the long-term metabolic and skeletal consequences of two commonly used C57BL/6 substrains to a high fat (HF) diet. Male C57BL/6J, C57BL/6N, and the negative control strain, C3H/HeJ, mice were fed a control or HF diet for 24 wks. C57BL/6N mice on a HF diet demonstrated an increase in plasma insulin and blood glucose as early as 4 wk, whereas these responses were delayed in the C57BL/6J mice. The C57BL/6N mice exhibited more severe hepatic steatosis and inflammation. Only the C57BL/6N mice lost significant trabecular bone in response to the high fat diet. The C3H/HeJ mice were protected from bone loss. The data show that C57BL/6J and C57BL/6N mice differ in their metabolic and skeletal response when fed a HF diet. These substrain differences should be considered when designing experiments and are likely to have implications on data interpretation and reproducibility. Hindawi Publishing Corporation 2015 2015-06-03 /pmc/articles/PMC4469802/ /pubmed/26146567 http://dx.doi.org/10.1155/2015/758080 Text en Copyright © 2015 Elizabeth Rendina-Ruedy et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Rendina-Ruedy, Elizabeth
Hembree, Kelsey D.
Sasaki, Angela
Davis, McKale R.
Lightfoot, Stan A.
Clarke, Stephen L.
Lucas, Edralin A.
Smith, Brenda J.
A Comparative Study of the Metabolic and Skeletal Response of C57BL/6J and C57BL/6N Mice in a Diet-Induced Model of Type 2 Diabetes
title A Comparative Study of the Metabolic and Skeletal Response of C57BL/6J and C57BL/6N Mice in a Diet-Induced Model of Type 2 Diabetes
title_full A Comparative Study of the Metabolic and Skeletal Response of C57BL/6J and C57BL/6N Mice in a Diet-Induced Model of Type 2 Diabetes
title_fullStr A Comparative Study of the Metabolic and Skeletal Response of C57BL/6J and C57BL/6N Mice in a Diet-Induced Model of Type 2 Diabetes
title_full_unstemmed A Comparative Study of the Metabolic and Skeletal Response of C57BL/6J and C57BL/6N Mice in a Diet-Induced Model of Type 2 Diabetes
title_short A Comparative Study of the Metabolic and Skeletal Response of C57BL/6J and C57BL/6N Mice in a Diet-Induced Model of Type 2 Diabetes
title_sort comparative study of the metabolic and skeletal response of c57bl/6j and c57bl/6n mice in a diet-induced model of type 2 diabetes
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4469802/
https://www.ncbi.nlm.nih.gov/pubmed/26146567
http://dx.doi.org/10.1155/2015/758080
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