tissue strain
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2021 ◽  
Author(s):  
Anne-Lise Duroy ◽  
Valerie Detti ◽  
Agnes Coulon ◽  
Olivier Basset ◽  
Elisabeth Brusseau




Author(s):  
Benjamin E. Peterson ◽  
Rebecca A. Rolfe ◽  
Allen Kunselman ◽  
Paula Murphy ◽  
Spencer E. Szczesny

During embryonic development, tendons transform into a hypocellular tissue with robust tensile load-bearing capabilities. Previous work suggests that this mechanical transformation is due to increases in collagen fibril length and is dependent on mechanical stimulation via muscle activity. However, the relationship between changes in the microscale tissue structure and changes in macroscale tendon mechanics is still unclear. Additionally, the specific effect of mechanical stimulation on the multiscale structure-function relationships of developing tendons is also unknown. Therefore, the objective of this study was to measure the changes in tendon mechanics and structure at multiple length scales during embryonic development with and without skeletal muscle paralysis. Tensile testing of tendons from chick embryos was performed to determine the macroscale tensile modulus as well as the magnitude of the fibril strains and interfibrillar sliding with applied tissue strain. Embryos were also treated with either decamethonium bromide or pancuronium bromide to produce rigid or flaccid paralysis. Histology was performed to assess changes in tendon size, spacing between tendon subunits, and collagen fiber diameter. We found that the increase in the macroscale modulus observed with development is accompanied by an increase in the fibril:tissue strain ratio, which is consistent with an increase in collagen fibril length. Additionally, we found that flaccid paralysis reduced the macroscale tendon modulus and the fibril:tissue strain ratio, whereas less pronounced effects that were not statistically significant were observed with rigid paralysis. Finally, skeletal paralysis also reduced the size of collagen fibril bundles (i.e., fibers). Together, these data suggest that more of the applied tissue strain is transmitted to the collagen fibrils at later embryonic ages, which leads to an increase in the tendon macroscale tensile mechanics. Furthermore, our data suggest that mechanical stimulation during development is necessary to induce structural and mechanical changes at multiple physical length scales. This information provides valuable insight into the multiscale structure-function relationships of developing tendons and the importance of mechanical stimulation in producing a robust tensile load-bearing soft tissue.



2021 ◽  
Author(s):  
Benjamin E Peterson ◽  
Rebecca A. Rolfe ◽  
Allen Kunselman ◽  
Paula Murphy ◽  
Spencer E. Szczesny

During embryonic development, tendons transform into a hypocellular tissue with robust tensile load-bearing capabilities. Previous work suggests that this mechanical transformation is due to increases in collagen fibril length and is dependent on mechanical stimulation via muscle activity. However, the relationship between changes in the microscale tissue structure and changes in macroscale tendon mechanics is still unclear. Additionally, the specific effect of mechanical stimulation on the multiscale structure-function relationships of developing tendons is also unknown. Therefore, the objective of this study was to measure the changes in tendon mechanics and structure at multiple length scales during embryonic development with and without skeletal muscle paralysis. Tensile testing of tendons from chicken embryos was performed to determine the macroscale tensile modulus as well as the magnitude of the fibril strains and interfibrillar sliding with applied tissue strain. Embryos were also treated with either decamethonium bromide or pancuronium bromide to produce rigid or flaccid paralysis. Histology was performed to assess changes in tendon size, spacing between tendon subunits, and collagen fiber diameter. We found that the increase in the macroscale modulus observed with development is accompanied by an increase in the fibril:tissue strain ratio, which is consistent with an increase in collagen fibril length. Additionally, we found that flaccid paralysis reduced the macroscale tendon modulus and the fibril:tissue strain ratio, whereas less pronounced effects that were not statistically significant were observed with rigid paralysis. Finally, skeletal paralysis also reduced the size of collagen fibril bundles (i.e., fibers). Together, these data suggest that more of the applied tissue strain is transmitted to the collagen fibrils at later embryonic ages, which leads in an increase the tendon macroscale tensile mechanics. Furthermore, our data suggest that mechanical stimulation during development is necessary to induce structural and mechanical changes at multiple physical length scales. This information provides valuable insight into the multiscale structure-function relationships of developing tendons and the importance of mechanical stimulation in producing a robust tensile load-bearing soft tissue.



2021 ◽  
Vol 4 (4) ◽  
pp. 291-301
Author(s):  
Jaehong Lee ◽  
Stephan J. Ihle ◽  
Guglielmo Salvatore Pellegrino ◽  
Hwajoong Kim ◽  
Junwoo Yea ◽  
...  




2020 ◽  
Vol 64 (1-4) ◽  
pp. 1373-1380
Author(s):  
Wenguang Zhang ◽  
Xuele Yin ◽  
Xuhui Zhou

In order to develop long-lifetime neural electrodes, the insertion tissue injury caused by two optimized neural electrode (convex streamline electrode and vibration attenuation electrode) models were evaluated compared with a reference electrode. Based on the experimental evaluation system for testing tissue injury, the effects of insertion speeds on tissue injury of the two optimized electrodes with different insertion depths were studied. The maximum tissue strain caused by the two optimized neural electrodes firstly increased and then decreased with the increase of insertion speed at the depths of 3 mm and 4.5 mm. The insertion forces caused by vibration attenuation electrode are steady with the change of insertion speed. The convex streamline neural electrode caused less tissue injury compared with the other two electrodes. The higher or lower insertion speed causes smaller tissue strain for the two optimized electrodes, which is conductive to set implantation parameters to minimize tissue injury.



2020 ◽  
Vol 64 (1-4) ◽  
pp. 1401-1409
Author(s):  
Wenguang Zhang ◽  
Xuele Yin ◽  
Jie Xie ◽  
Yakun Ma ◽  
Zhengwei Li

In order to develop long-lifetime neural electrodes, the insertion tissue injury caused by two optimized neural electrode (convex streamline electrode and vibration attenuation electrode) models were evaluated compared with a reference electrode. Based on the experimental evaluation system for testing tissue injury, the effects of insertion speeds on tissue injury of the two optimized electrodes with different insertion depths were studied. The maximum tissue strain caused by the two optimized neural electrodes firstly increased and then decreased with the increase of insertion speed at the depths of 3 mm and 4.5 mm. The insertion forces caused by vibration attenuation electrode are steady with the change of insertion speed. The convex streamline neural electrode caused less tissue injury compared with the other two electrodes. The higher or lower insertion speed causes smaller tissue strain for the two optimized electrodes, which is conductive to set implantation parameters to minimize tissue injury.



Author(s):  
Karen Taylor ◽  
T Blaine Hoshizaki ◽  
Andrew Post ◽  
Michael D Gilchrist

Impact parameters used to design the American football helmet and the parameters associated with mechanisms of concussive injury are not consistent. Head impacts resulting in concussive injury in football are characterized as events creating rotational motion of the head that generate brain tissue strain. The extent of tissue strain influences the resulting severity of injury. Helmet technology aimed to decrease brain tissue strain by reducing the extent of brain motion could help reduce injury risk. Current helmet performance and evaluation measures, such as peak resultant of linear and rotational acceleration, do not fully define directional brain motion and therefore cannot provide sufficient information for this type of improvement. This study was conducted to determine whether coordinate components (X, Y, and Z) of linear and rotational acceleration would correlate with maximum principal strain, a common measure of brain injury risk. Coordinate components define directional motion of the head and offer a specific design parameter more easily reduced using engineered structures than peak resultant acceleration. In addition to coordinate components, this study introduces the dominant component, defined as the coordinate component with the highest contribution to the resultant acceleration, for additional evaluation. The results show that the relationship between the X, Y, and Z coordinate components of acceleration and maximum principal strain is location- and direction-dependent. The study indicates a strong relationship between the peak resultant and dominant components of acceleration to maximum principal strain. Because the dominant component of acceleration accounts for direction and location, identifying the relationship between dominant acceleration and maximum principal strain demonstrates the potential use of this metric to improve future helmet innovation aimed at reducing tissue strain.



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