scholarly journals A Single Axial Impact Load Causes Articular Damage That Is Not Visible with Micro-Computed Tomography: An Ex Vivo Study on Caprine Tibiotalar Joints

Cartilage ◽  
2019 ◽  
pp. 194760351987635 ◽  
Author(s):  
Robin P. Blom ◽  
Douwe Mol ◽  
Leo J. van Ruijven ◽  
Gino M. M. J. Kerkhoffs ◽  
Theo H. Smit

Objective Excessive articular loading, for example, an ankle sprain, may result in focal osteochondral damage, initiating a vicious degenerative process resulting in posttraumatic osteoarthritis (PTOA). Better understanding of this degenerative process would allow improving posttraumatic care with the aim to prevent PTOA. The primary objective of this study was to establish a drop-weight impact testing model with controllable, reproducible and quantitative axial impact loads to induce osteochondral damage in caprine tibiotalar joints. We aimed to induce osteochondral damage on microscale level of the tibiotalar joint without gross intra-articular fractures of the tibial plafond. Design Fresh-frozen tibiotalar joints of mature goats were used as ex vivo articulating joint models. Specimens were axially impacted by a mass of 10.5 kg dropped from a height of 0.3 m, resulting in a speed of 2.4 m/s, an impact energy of 31.1 J and an impact impulse of 25.6 N·s. Potential osteochondral damage of the caprine tibiotalar joints was assessed using contrast-enhanced high-resolution micro-computed tomography (micro-CT). Subsequently, we performed quasi-static loading experiments to determine postimpact mechanical behavior of the tibiotalar joints. Results Single axial impact loads with a mass of 15.5 kg dropped from 0.3 m, resulted in intra-articular fractures of the tibial plafond, where a mass of 10.55 kg dropped from 0.3 m did not result in any macroscopic damage. In addition, contrast-enhanced high-resolution micro-CT imaging neither reveal any acute microdamage (i.e., microcracks) of the subchondral bone nor any (micro)structural changes in articular cartilage. The Hexabrix content or voxel density (i.e., proteoglycan content of the articular cartilage) on micro-CT did not show any differences between intact and impacted specimens. However, quasi-static whole-tibiotalar-joint loading showed an altered biomechanical behavior after application of a single axial impact (i.e., increased hysteresis when compared with the intact or nonimpacted specimens). Conclusions Single axial impact loads did not induce osteochondral damage visible with high-resolution contrast-enhanced micro-CT. However, despite the lack of damage on macro- and even microscale, the single axial impact loads resulted in “invisible injuries” because of the observed changes in the whole-joint biomechanics of the caprine tibiotalar joints. Future research must focus on diagnostic tools for the detection of early changes in articular cartilage after a traumatic impact (i.e., ankle sprains or ankle fractures), as it is well known that this could result in PTOA.

2016 ◽  
Vol 24 ◽  
pp. S277-S278
Author(s):  
H. Gahunia ◽  
S. Karhula ◽  
T. Ylitalo ◽  
E. Hæggström ◽  
K.P. Pritzker ◽  
...  

2004 ◽  
Vol 12 (8) ◽  
pp. 614-626 ◽  
Author(s):  
Danika L. Batiste ◽  
Alexandra Kirkley ◽  
Sheila Laverty ◽  
Lisa M.F. Thain ◽  
Alison R. Spouge ◽  
...  

2021 ◽  
Author(s):  
Eva Chatzinikolaou ◽  
Kleoniki Keklikoglou

Micro-computed tomography (micro-CT) is a high-resolution 3D-imaging technique which is now increasingly applied in biological studies focusing on taxonomy and functional morphology. The creation of virtual representations of specimens can increase availability of otherwise underexploited and inaccessible samples. This protocol aims to standardise micro-CT scanning procedures for embryos and juveniles of the marine gastropod species Hexaplex trunculus.


2018 ◽  
Vol 314 (3) ◽  
pp. F493-F499 ◽  
Author(s):  
Ruslan Hlushchuk ◽  
Cédric Zubler ◽  
Sébastien Barré ◽  
Carlos Correa Shokiche ◽  
Laura Schaad ◽  
...  

In the last decades, the contrast-enhanced micro-computed tomography (micro-CT) imaging of a whole animal kidney became increasingly important. The visualization was mainly limited to middle-sized vessels. Since modern desktop micro-CT scanners provide the necessary detail resolution, we developed an approach for rapid visualization and consistent assessment of kidney vasculature and glomeruli number. This method is based on μAngiofil, a new polymerizing contrast agent with homogenous X-ray absorption, which provides continuous filling of the complete vasculature and enables correlative imaging approaches. For rapid and reliable kidney morphometry, the microangio-CT (µaCT) data sets from glial cell line-derived neurotrophic factor (GDNF)+/− mice and their wild-type littermates were used. The results were obtained much faster compared with the current gold standard, histology-based stereology, and without processing artifacts. The histology-based morphometry was done afterward on the same kidneys. Both approaches revealed that the GDNF+/− male mice had about 40% fewer glomeruli. Furthermore, our approach allows for the definition of sites of interest for further histological investigation, i.e., correlative morphology. The polymerized μAngiofil stays in perfused vessels and is autofluorescent, which is what greatly facilitates the matching of histological sections with µaCT data. The presented approach is a time-efficient, reliable, qualitative, and quantitative methodology. Besides glomerular morphometry, the µaCT data can be used for qualitative and quantitative analysis of the kidney vasculature and correlative morphology.


2017 ◽  
Vol 35 (12) ◽  
pp. 2740-2748 ◽  
Author(s):  
Maleeha Mashiatulla ◽  
Meghan M. Moran ◽  
Deva Chan ◽  
Jun Li ◽  
Jonathan D. Freedman ◽  
...  

2016 ◽  
Vol 13 (123) ◽  
pp. 20160589
Author(s):  
James Rafferty ◽  
Lance Farr ◽  
Tim James ◽  
David Chase ◽  
John Heinrich ◽  
...  

We present a novel, high-resolution magnetic resonance technique, fine structure analysis (FSA) for the quantification and analysis of amorphous and quasi-amorphous biological structures. The one-dimensional technique is introduced mathematically and then applied to one simulated phantom, two physical phantoms and a set of ex vivo biological samples, scanned with interpoint spacings of 0.0038–0.195 mm and cross-sectional sizes of 3 × 3 or 5 × 5 mm. The simulated phantom and one of the physical phantoms consists of randomly arranged beads of known size in two and three dimensions, respectively. The second physical phantom was constructed by etching lines on Perspex. The ex vivo samples are human bone specimens. We show that for all three phantoms, the FSA technique is able to elucidate the average spacing of the structures present within each sample using structural spectroscopy, the smallest of which was 180 µm in size. We further show that in samples of trabecular bone, FSA is able to produce comparable results to micro-computed tomography, the current gold standard for measuring bone microstructure, but without the need for ionizing radiation. Many biological structures are too small to be captured by conventional, clinically deployed medical imaging techniques. FSA has the potential for use in the analysis of pathologies where such small-scale repeating structures are disrupted or their size, and spacing is otherwise altered.


2020 ◽  
Vol 237 (6) ◽  
pp. 1062-1071
Author(s):  
Colet E. M. Voert ◽  
R. Y. Nigel Kour ◽  
Bente C. J. Teeffelen ◽  
Niloufar Ansari ◽  
Kathryn S. Stok

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