Quantification of Age-Related Tissue-Level Failure Strains of Rat Femoral Cortical Bones Using an Approach Combining Macrocompressive Test and Microfinite Element Analysis

2016 ◽  
Vol 138 (4) ◽  
Author(s):  
Ruoxun Fan ◽  
He Gong ◽  
Rui Zhang ◽  
Jiazi Gao ◽  
Zhengbin Jia ◽  
...  

Bone mechanical properties vary with age; meanwhile, a close relationship exists among bone mechanical properties at different levels. Therefore, conducting multilevel analyses for bone structures with different ages are necessary to elucidate the effects of aging on bone mechanical properties at different levels. In this study, an approach that combined microfinite element (micro-FE) analysis and macrocompressive test was established to simulate the failure of male rat femoral cortical bone. Micro-FE analyses were primarily performed for rat cortical bones with different ages to simulate their failure processes under compressive load. Tissue-level failure strains in tension and compression of these cortical bones were then back-calculated by fitting the experimental stress–strain curves. Thus, tissue-level failure strains of rat femoral cortical bones with different ages were quantified. The tissue-level failure strain exhibited a biphasic behavior with age: in the period of skeletal maturity (1–7 months of age), the failure strain gradually increased; when the rat exceeded 7 months of age, the failure strain sharply decreased. In the period of skeletal maturity, both the macro- and tissue-levels mechanical properties showed a large promotion. In the period of skeletal aging (9–15 months of age), the tissue-level mechanical properties sharply deteriorated; however, the macromechanical properties only slightly deteriorated. The age-related changes in tissue-level failure strain were revealed through the analysis of male rat femoral cortical bones with different ages, which provided a theoretical basis to understand the relationship between rat cortical bone mechanical properties at macro- and tissue-levels and decrease of bone strength with age.

2009 ◽  
Vol 22 (03) ◽  
pp. 210-215 ◽  
Author(s):  
C.A. Phillips ◽  
S.A. Fernandez ◽  
Y. Li ◽  
S.S. Huja

Summary Objectives: The purpose of this study was to quantify the tissue level mechanical properties of cortical bone of skeletally immature (~five-month-old) Beagle dogs and compare them to data from mature dogs measured in a previous study. Methods: Eight femoral cross sectional specimens (two bone sections / dog) were obtained from four skeletally immature dogs. A pair of calcein bone labels were administered intravenously to the dogs to mark sites of active mineralization prior to euthanasia. Prepared bone specimens were placed in a nanoindenter specimen holder and the previously identified calcein labelled osteons were located. Labelled (n = 128) and neighbouring unlabelled (n = 127) osteons in skeletally immature femurs were examined by instrumented indentation testing. Indents were made to a depth of 500 nm at a loading rate of 10 nm/s. Indentation modulus (IM) and hardness (H) were obtained. Results: The overall IM of the cortical bone in the skeletally mature groups was significantly greater than in the immature group (p = 0.0011), however overall H was not significantly different. The differences between the groups in IM were significant for the unlabelled osteons (p = 0.001), but not for the labelled osteons (p = 0.56). Conclusion: There are differences in the IM of unlabelled osteons in skeletally immature and mature groups of Beagle dogs. In contrast to whole bone mechanical tests, where there are obvious differences between growing and mature bones, there are only small differences in the micro-mechanical properties.


2015 ◽  
Vol 15 (05) ◽  
pp. 1550074 ◽  
Author(s):  
MICHAEL CHITTENDEN ◽  
AHMAD RAEISI NAJAFI ◽  
JUN LI ◽  
IWONA JASIUK

Composition-structure-property relations of bone provide fundamental understanding of bone quality. The objective of this paper was to investigate age dependent changes in the composition, structure and mechanical properties of porcine femoral cortical bone at mid-diaphysis region from six age groups (1, 3.5, 6, 12, 30, 48 months). This study was motivated by the fact that limited data is available in the literature on young porcine cortical bone. Nanoindentation technique with Berkovich fluid cell tip was employed to measure the elastic modulus and hardness. Individual lamellae were indented in the longitudinal direction of bone in different microstructural components (osteonal, interstitial and plexiform bone). A grid of indentations was also made on one bone sample to obtain spatial variations in the elastic modulus and hardness. Ash and water content tests were performed to measure water, organic and mineral contents of bone as a function of age. Finally, high resolution micro-computed tomography was used to measure porosity and visualize three-dimensional void structures. We found that the elastic modulus and hardness of bone increased with age but at different rates in each microstructural component. The mineral content increased correspondingly with age while the porosity decreased. The obtained structure, composition, and mechanical properties data give new insights on the age related changes in young cortical bone and can serve as inputs for and validation of multiscale models of bone.


eLife ◽  
2021 ◽  
Vol 10 ◽  
Author(s):  
Yoanna Ariosa-Morejon ◽  
Alberto Santos ◽  
Roman Fischer ◽  
Simon Davis ◽  
Philip Charles ◽  
...  

Collagen-rich tissues have poor reparative capacity that predisposes to common age-related disorders such as osteoporosis and osteoarthritis. We used in vivo pulsed SILAC labelling to quantify new protein incorporation into cartilage, bone, and skin of mice across the healthy life course. We report dynamic turnover of the matrisome, the proteins of the extracellular matrix, in bone and cartilage during skeletal maturation, which was markedly reduced after skeletal maturity. Comparing young adult with older adult mice, new protein incorporation was reduced in all tissues. STRING clustering revealed changes in epigenetic modulators across all tissues, a decline in chondroprotective growth factors such as FGF2 and TGFβ in cartilage, and clusters indicating mitochondrial dysregulation and reduced collagen synthesis in bone. Several pathways were implicated in age-related disease. Fewer changes were observed for skin. This methodology provides dynamic protein data at a tissue level, uncovering age-related molecular changes that may predispose to disease.


Endocrinology ◽  
1996 ◽  
Vol 137 (4) ◽  
pp. 1358-1364 ◽  
Author(s):  
J Aerssens ◽  
R van Audekercke ◽  
M Talalaj ◽  
P Geusens ◽  
E Bramm ◽  
...  

2014 ◽  
Vol 29 (10) ◽  
pp. 1135-1143 ◽  
Author(s):  
Sebastián Jaramillo Isaza ◽  
Pierre-Emmanuel Mazeran ◽  
Karim El Kirat ◽  
Marie-Christine Ho Ba Tho

Abstract


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