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Changes in bone macro- and microstructure in diabetic obese mice revealed by high resolution microfocus X-ray computed tomography

High resolution microfocus X-ray computed tomography (HR-microCT) was employed to characterize the structural alterations of the cortical and trabecular bone in a mouse model of obesity-driven type 2 diabetes (T2DM). C57Bl/6J mice were randomly assigned for 14 weeks to either a control diet-fed (CTR...

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Autores principales: Kerckhofs, G., Durand, M., Vangoitsenhoven, R., Marin, C., Van der Schueren, B., Carmeliet, G., Luyten, F. P., Geris, L., Vandamme, K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5069481/
https://www.ncbi.nlm.nih.gov/pubmed/27759061
http://dx.doi.org/10.1038/srep35517
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author Kerckhofs, G.
Durand, M.
Vangoitsenhoven, R.
Marin, C.
Van der Schueren, B.
Carmeliet, G.
Luyten, F. P.
Geris, L.
Vandamme, K.
author_facet Kerckhofs, G.
Durand, M.
Vangoitsenhoven, R.
Marin, C.
Van der Schueren, B.
Carmeliet, G.
Luyten, F. P.
Geris, L.
Vandamme, K.
author_sort Kerckhofs, G.
collection PubMed
description High resolution microfocus X-ray computed tomography (HR-microCT) was employed to characterize the structural alterations of the cortical and trabecular bone in a mouse model of obesity-driven type 2 diabetes (T2DM). C57Bl/6J mice were randomly assigned for 14 weeks to either a control diet-fed (CTRL) or a high fat diet (HFD)-fed group developing obesity, hyperglycaemia and insulin resistance. The HFD group showed an increased trabecular thickness and a decreased trabecular number compared to CTRL animals. Midshaft tibia intracortical porosity was assessed at two spatial image resolutions. At 2 μm scale, no change was observed in the intracortical structure. At 1 μm scale, a decrease in the cortical vascular porosity of the HFD bone was evidenced. The study of a group of 8 week old animals corresponding to animals at the start of the diet challenge revealed that the decreased vascular porosity was T2DM-dependant and not related to the ageing process. Our results offer an unprecedented ultra-characterization of the T2DM compromised skeletal micro-architecture and highlight an unrevealed T2DM-related decrease in the cortical vascular porosity, potentially affecting the bone health and fragility. Additionally, it provides some insights into the technical challenge facing the assessment of the rodent bone structure using HR-microCT imaging.
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spelling pubmed-50694812016-10-26 Changes in bone macro- and microstructure in diabetic obese mice revealed by high resolution microfocus X-ray computed tomography Kerckhofs, G. Durand, M. Vangoitsenhoven, R. Marin, C. Van der Schueren, B. Carmeliet, G. Luyten, F. P. Geris, L. Vandamme, K. Sci Rep Article High resolution microfocus X-ray computed tomography (HR-microCT) was employed to characterize the structural alterations of the cortical and trabecular bone in a mouse model of obesity-driven type 2 diabetes (T2DM). C57Bl/6J mice were randomly assigned for 14 weeks to either a control diet-fed (CTRL) or a high fat diet (HFD)-fed group developing obesity, hyperglycaemia and insulin resistance. The HFD group showed an increased trabecular thickness and a decreased trabecular number compared to CTRL animals. Midshaft tibia intracortical porosity was assessed at two spatial image resolutions. At 2 μm scale, no change was observed in the intracortical structure. At 1 μm scale, a decrease in the cortical vascular porosity of the HFD bone was evidenced. The study of a group of 8 week old animals corresponding to animals at the start of the diet challenge revealed that the decreased vascular porosity was T2DM-dependant and not related to the ageing process. Our results offer an unprecedented ultra-characterization of the T2DM compromised skeletal micro-architecture and highlight an unrevealed T2DM-related decrease in the cortical vascular porosity, potentially affecting the bone health and fragility. Additionally, it provides some insights into the technical challenge facing the assessment of the rodent bone structure using HR-microCT imaging. Nature Publishing Group 2016-10-19 /pmc/articles/PMC5069481/ /pubmed/27759061 http://dx.doi.org/10.1038/srep35517 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Kerckhofs, G.
Durand, M.
Vangoitsenhoven, R.
Marin, C.
Van der Schueren, B.
Carmeliet, G.
Luyten, F. P.
Geris, L.
Vandamme, K.
Changes in bone macro- and microstructure in diabetic obese mice revealed by high resolution microfocus X-ray computed tomography
title Changes in bone macro- and microstructure in diabetic obese mice revealed by high resolution microfocus X-ray computed tomography
title_full Changes in bone macro- and microstructure in diabetic obese mice revealed by high resolution microfocus X-ray computed tomography
title_fullStr Changes in bone macro- and microstructure in diabetic obese mice revealed by high resolution microfocus X-ray computed tomography
title_full_unstemmed Changes in bone macro- and microstructure in diabetic obese mice revealed by high resolution microfocus X-ray computed tomography
title_short Changes in bone macro- and microstructure in diabetic obese mice revealed by high resolution microfocus X-ray computed tomography
title_sort changes in bone macro- and microstructure in diabetic obese mice revealed by high resolution microfocus x-ray computed tomography
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5069481/
https://www.ncbi.nlm.nih.gov/pubmed/27759061
http://dx.doi.org/10.1038/srep35517
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