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Estrogen depletion and drug treatment alter the microstructure of type I collagen in bone

The impact of estrogen depletion and drug treatment on type I collagen fibril nanomorphology and collagen fibril packing (microstructure) was evaluated by atomic force microscopy (AFM) using an ovariectomized (OVX) rabbit model of estrogen deficiency induced bone loss. Nine month-old New Zealand whi...

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Autores principales: Cauble, Meagan A., Muckley, Matthew J., Fang, Ming, Fessler, Jeffrey A., Welch, Kathleen, Rothman, Edward D., Orr, Bradford G., Duong, Le T., Holl, Mark M. Banaszak
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5440968/
https://www.ncbi.nlm.nih.gov/pubmed/28580393
http://dx.doi.org/10.1016/j.bonr.2016.08.003
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author Cauble, Meagan A.
Muckley, Matthew J.
Fang, Ming
Fessler, Jeffrey A.
Welch, Kathleen
Rothman, Edward D.
Orr, Bradford G.
Duong, Le T.
Holl, Mark M. Banaszak
author_facet Cauble, Meagan A.
Muckley, Matthew J.
Fang, Ming
Fessler, Jeffrey A.
Welch, Kathleen
Rothman, Edward D.
Orr, Bradford G.
Duong, Le T.
Holl, Mark M. Banaszak
author_sort Cauble, Meagan A.
collection PubMed
description The impact of estrogen depletion and drug treatment on type I collagen fibril nanomorphology and collagen fibril packing (microstructure) was evaluated by atomic force microscopy (AFM) using an ovariectomized (OVX) rabbit model of estrogen deficiency induced bone loss. Nine month-old New Zealand white female rabbits were treated as follows: sham-operated (Sham; n = 11), OVX + vehicle (OVX + Veh; n = 12), OVX + alendronate (ALN, 600 μg/kg/wk., s.c.; n = 12), and OVX + cathepsin-K inhibitor L-235 (CatKI, 10 mg/kg, daily, p.o.; n = 13) in prevention mode for 27 weeks. Samples from the cortical femur and trabecular lumbar vertebrae were polished, demineralized, and imaged using AFM. Auto-correlation of image patches was used to generate a vector field for each image that mathematically approximated the collagen fibril alignment. This vector field was used to compute an information-theoretic entropy that was employed as a quantitative fibril alignment parameter (FAP) to allow image-to-image and sample-to-sample comparison. For all samples, no change was observed in the average FAP values; however significant differences in the distribution of FAP values were observed. In particular, OVX + Veh lumbar vertebrae samples contained a tail of lower FAP values representing regions of greater fibril alignment. OVX + ALN treatment resulted in a FAP distribution with a tail indicating greater alignment for cortical femur and less alignment for trabecular lumbar vertebrae. OVX + CatKI treatment gave a distribution of FAP values with a tail indicating less alignment for cortical femur and no change for trabecular lumbar vertebrae. Fibril alignment was also evaluated by considering when a fibril was part of discrete bundles or sheets (classified as parallel) or not (classified as oblique). For this analysis, the percentage of parallel fibrils in cortical femur for the OVX group was 17% lower than the Sham group. OVX + ALN treatment partially prevented the proportion of parallel fibrils from decreasing and OVX + CatKI treatment completely prevented a change. In trabecular lumbar vertebrae, there was no difference in the percentage of parallel fibrils between Sham and any of the other treatment groups.
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spelling pubmed-54409682017-06-02 Estrogen depletion and drug treatment alter the microstructure of type I collagen in bone Cauble, Meagan A. Muckley, Matthew J. Fang, Ming Fessler, Jeffrey A. Welch, Kathleen Rothman, Edward D. Orr, Bradford G. Duong, Le T. Holl, Mark M. Banaszak Bone Rep Article The impact of estrogen depletion and drug treatment on type I collagen fibril nanomorphology and collagen fibril packing (microstructure) was evaluated by atomic force microscopy (AFM) using an ovariectomized (OVX) rabbit model of estrogen deficiency induced bone loss. Nine month-old New Zealand white female rabbits were treated as follows: sham-operated (Sham; n = 11), OVX + vehicle (OVX + Veh; n = 12), OVX + alendronate (ALN, 600 μg/kg/wk., s.c.; n = 12), and OVX + cathepsin-K inhibitor L-235 (CatKI, 10 mg/kg, daily, p.o.; n = 13) in prevention mode for 27 weeks. Samples from the cortical femur and trabecular lumbar vertebrae were polished, demineralized, and imaged using AFM. Auto-correlation of image patches was used to generate a vector field for each image that mathematically approximated the collagen fibril alignment. This vector field was used to compute an information-theoretic entropy that was employed as a quantitative fibril alignment parameter (FAP) to allow image-to-image and sample-to-sample comparison. For all samples, no change was observed in the average FAP values; however significant differences in the distribution of FAP values were observed. In particular, OVX + Veh lumbar vertebrae samples contained a tail of lower FAP values representing regions of greater fibril alignment. OVX + ALN treatment resulted in a FAP distribution with a tail indicating greater alignment for cortical femur and less alignment for trabecular lumbar vertebrae. OVX + CatKI treatment gave a distribution of FAP values with a tail indicating less alignment for cortical femur and no change for trabecular lumbar vertebrae. Fibril alignment was also evaluated by considering when a fibril was part of discrete bundles or sheets (classified as parallel) or not (classified as oblique). For this analysis, the percentage of parallel fibrils in cortical femur for the OVX group was 17% lower than the Sham group. OVX + ALN treatment partially prevented the proportion of parallel fibrils from decreasing and OVX + CatKI treatment completely prevented a change. In trabecular lumbar vertebrae, there was no difference in the percentage of parallel fibrils between Sham and any of the other treatment groups. Elsevier 2016-08-27 /pmc/articles/PMC5440968/ /pubmed/28580393 http://dx.doi.org/10.1016/j.bonr.2016.08.003 Text en © 2016 The Author(s) http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Cauble, Meagan A.
Muckley, Matthew J.
Fang, Ming
Fessler, Jeffrey A.
Welch, Kathleen
Rothman, Edward D.
Orr, Bradford G.
Duong, Le T.
Holl, Mark M. Banaszak
Estrogen depletion and drug treatment alter the microstructure of type I collagen in bone
title Estrogen depletion and drug treatment alter the microstructure of type I collagen in bone
title_full Estrogen depletion and drug treatment alter the microstructure of type I collagen in bone
title_fullStr Estrogen depletion and drug treatment alter the microstructure of type I collagen in bone
title_full_unstemmed Estrogen depletion and drug treatment alter the microstructure of type I collagen in bone
title_short Estrogen depletion and drug treatment alter the microstructure of type I collagen in bone
title_sort estrogen depletion and drug treatment alter the microstructure of type i collagen in bone
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5440968/
https://www.ncbi.nlm.nih.gov/pubmed/28580393
http://dx.doi.org/10.1016/j.bonr.2016.08.003
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