Passive Mechanical Properties Research Articles

Characterizing the interaction effects of modular components on transtibial prosthesis stance-phase mechanical behavior

Background: Despite evidence that passive prosthesis mechanical properties can directly affect user experience, prosthetists have access to minimal information regarding the mechanical interactions between a prosthetic foot and proximal modular componentry. Objectives: This study quantified the stance phase mechanical behavior of a transtibial prosthetic system through the addition of passive modular componentry to a dynamic response (DR) foot. Study Design: Repeated measures, mechanical characterization. Methods: Maximum displacement and energy return were measured with a materials test machine simulating initial, mid, and terminal stances. Twelve conditions were tested: a DR foot in combination with a hydraulic ankle at 2 resistance settings and 3 different shock-absorbing pylons (SAPs). The roll-over shape of the DR foot with and without hydraulic ankle was measured using a test rig. Results: Adding modular passive components altered displacement and energy return, displaying independent and interaction effects. Generally, the hydraulic ankle and SAP reduced energy return (up to 18%) but decreased (up to 51%) and increased (up to 88%) displacement, respectively, while the combined properties were more complex. Roll-over shape radii decreased with increasing load for the foot alone but exhibited a nonlinear response with the addition of the ankle. Conclusions: Inclusion of modular components in a transtibial prosthetic system can have complex mechanical interactions that independently affect the system's response to load. It is important for clinicians to be aware of the cumulative effects of these interactions to inform the tuning of transtibial prosthesis mechanical behavior. Combinations of hydraulic ankles and SAPs can help clinicians adjust the prosthesis to achieve a balance between user comfort and energy return.

Effect of Skeletal Muscle Immobilization on Regional Anisotropic Viscohyperelastic Properties Change in a Rat Model

Passive mechanical properties in three different zones (distal, proximal, and medial) of biceps brachii immobilized in short position and its free contralateral were investigated. For that, in vitro equibiaxial relaxation tests were performed with samples harvested from skeletal muscles of immobilized rats during one or two weeks. From data obtained in two plane axes of loading, a viscohyperelastic anisotropic model described by a strain energy function coupled with second order Maxwell's model, was used to identify the material parameters. It has been shown that the zone influences the material parameters of the hyperelasticity behavior while the immobilization acts rather on the viscoelasticity response. Based on measurements of histological parameters from flexor carpi ulnaris muscles, we observed that immobilization produced contractile tissue atrophy and connective tissue thickening. The muscle atrophy caused by immobilization could lead to a more linear mechanical behavior along the axis of the muscle fibers. Furthermore, fibrosis, quantified by histological analysis on flexor carpi ulnaris muscles, could result in highly non-linear behavior along the other axis. These structural changes also contribute to an increase in relaxation following immobilization along both axes (+11.7% and +15.5% on average with p < 0.001 and p < 0.01 respectively for each axis). Statement of significanceTo our best knowledge, this work is the first to investigate the anisotropic, viscohyperelastic and heterogeneous properties within a passive skeletal muscle immobilized in a short position. For that, from a rat model, equibiaxial relaxation tests were performed and material parameters were found from a strain energy function coupled with a Maxwell's model. We showed that excising zone of samples greatly influences the parameters of the hyperelastic behavior while the immobilization influences the viscoelasticity response instead. Furthermore, histological analysis permitted to quantify fibrosis in the skeletal muscle and bear out, at least in part, changes in relaxation behavior following immobilization.

Study on the compressive performance of hyperelastic seismic isolation materials under passive confinement of surrounding rock simulated by CFRP tubes

Tunnel engineering has played a significant role in the development of human society. However, due to geological constraints, tunnels are prone to losing stability and safety under strong seismic forces. High-elasticity, super-tough polymer-inorganic composite tunnel isolation materials (PTIM), based on polyurethane elastomers, can meet the requirements for tunnel isolation, but research on their passive confinement mechanical properties remains insufficient. This study designed an experimental method to simulate the passive confinement state of tunnel isolation materials. The method uses CFRP tube confinement and core loading to replicate the actual stress conditions within a confined tunnel space. Based on the experimental data, a constitutive model for PTIM under passive confinement was established. The results show that the initial elastic modulus (Ec0) of PTIM and the CFRP confinement stiffness (K) are significantly correlated with the material's stress-strain curve, axial peak stress and strain, circumferential strain, compressive performance, and elastic modulus. Based on these mechanical properties as characteristic values, a tri-linear constitutive model for PTIM with different mix ratios under various confinement stress conditions was established. The high degree of agreement between the predicted data and the experimental data validates the effectiveness of the model.

Modeling implications of the relationship between active and passive skeletal muscle mechanical properties

It is challenging to obtain in vivo or in situ experimental data from human muscles due to the invasive nature of such measurements. As a result, many investigations of human performance, surgery, or skeletal adaptation are necessarily based on musculoskeletal models. The utility of such models will depend on the question being asked and the extent to which the model is sufficiently accurate to address that question. In this perspective article, we take advantage of unique intraoperative access to the human gracilis muscle and make direct comparisons between commonly modeled parameters and those measured from the human gracilis. We directly compare muscle–tendon unit (MTU) length, optimal fiber length, and tendon slack length. Our results demonstrate that measured and modeled length parameters differ greatly. This is primarily due to the fact that slack muscle length and optimal muscle length differ greatly for the human gracilis and that models assume they are the same length.

Impact of a 5-min massage session on the gastrocnemius contractile and passive mechanical properties in young adults - A randomized controlled trial

The analysis of the impact of a 5-min massage session on the gastrocnemius contractile and passive mechanical properties in young adults - a randomized controlled trial. BackgroundThe effect of massage therapy on the muscle properties is unclear. New technologies make investigation more in-depth and reliable. ObjectivesThis study examined the effects of a 5-min massage session on the muscle stiffness and tone reduction in healthy young adults. Materials and methodsParticipants aged between 19 and 24 were randomly assigned to an intervention group (IG) (n = 40) or a control group (CG) (n = 40). The IG participated in a 5-min massage session of the lateral and medial gastrocnemius muscle (LGCM and MGCM respectively). The muscle contractile properties were assessed by tensiomyography (TMG). It measured maximal displacement (Dm), delay time (Td) and contraction time (Tc). Oscillation frequency (F) and stiffness (S) were used to assess muscle passive mechanical properties. These measurements were collected by MytonPro. ResultsThere were no differences between the groups in the pre-test measurements. The results of mixed-model ANOVA showed significant (p < 0.05) time × group interactions, with greater alteration in the IG compared to the CG in the LGCM for Dm (%diff = 22.5, ƞp2 = 0.41), Td (%diff = 3.63, ƞp2 = 0.02), Tc (%diff = 13.38, ƞp2 = 0.1), F (%diff = 5.55, ƞp2 = 0.07) and in the MGCM for Dm (%diff = −14.34, ƞp2 = 0.06), F (%diff = −7.53, ƞp2 = 0.12). No difference (p > 0.05) was noticed in other variables. ConclusionsA 5-min massage session impacts the contractile and passive mechanical properties of the LGCM and MGCM. The size and direction of changes may depend on the muscle type, its geometry as well as other factors.

Mathematical modeling of biomechanical elastic and hyperelastic properties of the myocardium

BACKGROUND: The study of mechanical properties of biological tissues is extremely informative and is one of the most important areas of biomechanics. Knowledge of these aspects of biological objects based on experimental data can become a source of new medical and technical solutions for the reconstruction of organs and the development of replacement materials. AIM: Passive mechanical properties of isolated myocardium are compared with linear, bilinear, exponential and the most common hyperelastic models (neohookean, Mooney–Rivlin, Ogden, Yeoh, polynomial and Veronda–Westmann). MATERIALS AND METHODS: Literature data on mechanical tests of autopsy material obtained from mongrel dogs were used as initial data. To search for the most advanced calculation algorithms the computer algebra system was used, the Mathcad 15.0 software package and the multifunctional finite element analysis application ANSYS 2022 R2 were used. Direct comparison of models was made based on mathematical statistics. RESULTS: Among the first group of models, the results closest to the experimental data were demonstrated by the exponential model R = 0.9958/0.9984 (in the longitudinal/transverse direction with respect to the myocardial fibers), the lowest accuracy was demonstrated by the linear model R = 0.9813/0.9803. Young’s moduli of linear, bilinear and exponential models and material constants of hyperelastic models are determined. The coefficient of elastic anisotropy of the myocardium, defined as the ratio of the elastic moduli of the linear model measured along and across the direction of the fibers, is equal to 2.18, which is very different from the literature data for the myocardium of the human heart. Deformation along the fibers of the heart muscle is more energy-consuming in the direction along the fibers than in the transverse direction (3.81 and 2.52 mJ/cm3). The most accurate hyperelastic models turned out to be the 2nd order polynomial model R = 0.9971 and the 3rd order Yeoh model R = 0.997. The largest deviations and the lowest correlation coefficient between the experimental and model data were demonstrated by the simple neohookean model R = 0.974 with a single parameter μ. The numerical values of the parameters of hyperelastic models obtained by calculation methods used practically did not differ from each other (≤2.16%). CONCLUSIONS: The study demonstrated the importance of selecting the correct mechanical model for isolated myocardium. The data obtained can be useful in virtual interventions (simulations) for predicting outcomes and supporting clinical decisions, developing replacement materials and structures made of them for reconstructive operations on heart structures.

Passive mechanical properties of adipose tissue and skeletal muscle from C57BL/6J mice

Skeletal muscle and adipose tissue are characterized by unique structural features finely tuned to meet specific functional demands. In this study, we investigated the passive mechanical properties of soleus (SOL), extensor digitorum longus (EDL) and diaphragm (DIA) muscles, as well as subcutaneous (SAT), visceral (VAT) and brown (BAT) adipose tissues from 13 C57BL/6J mice. Thereto, alongside stress-relaxation assessments we subjected isolated muscles and adipose tissues (ATs) to force-extension tests up to 10% and 30% of their optimal length, respectively. Peak passive stress was highest in the DIA, followed by the SOL and lowest in the EDL (p < 0.05). SOL displayed also the highest Young's modulus and hysteresis among muscles (p < 0.05). BAT demonstrated highest peak passive stress and Young's modulus followed by VAT (p < 0.05), while SAT showed the highest hysteresis (p < 0.05). When comparing data across all six biological specimens at fixed passive force intervals (i.e., 20–40 and 50–70 mN), skeletal muscles exhibited significantly higher peak stresses and strains than ATs (p < 0.05). Young's modulus was higher in skeletal muscles than in ATs (p < 0.05). Muscle specimens exhibited slower force relaxation in the first phase compared to ATs (p < 0.05), while there was no significant difference in behavior between muscles and AT in the second phase of relaxation. The study revealed distinctive mechanical behaviors specific to different tissues, and even between different muscles and ATs. These variations in mechanical properties are likely such to optimize the specific functions performed by each biological tissue.

Allelic modulation of large (second-order) mesenteric artery mechanical properties in adult APOE3 &amp; APOE4 Mice

Previous studies from our lab have demonstrated age-related changes in vascular structure/function in posterior cerebral arteries (PCA) and left common carotid artery (CA) in male and female mice expressing human-APOE targeted replacement of APOE3 (B6.129P2-APOEtm2(APOE*3)MaeN8) and APOE4 (B6.129P2-APOEtm3(APOE*4)MaeN8) (Taconic Labs). Therefore, we hypothesize that similar changes may be observed in the systemic circulation. We isolated second-order mesenteric arteries (MA) from adult (6-month-old) male and female mice expressing APOE3 (n=3) and APOE4 (n=4). Mesenteric artery segments (5-8 mm in length) were rapidly isolated and cannulated on an arteriograph to assess mechanical properties: lumen diameter (LD), wall thickness (WT), wall:lumen ratio (W:L), distensibility, stress, strain, and stress versus strain (SvS) in the presence of Ca2+-free Krebs + diltiazem at intraluminal pressures ranging from 10mmHg–140mmHg. Phenylephrine and potassium-induced contractions were assessed in Ca2+-containing Krebs at intraluminal pressures ranging from 10-140mmHg. Data were analyzed using two-way ANOVA, Student’s t-test, and analysis of nonlinear fit. Values were considered statistically different at p&lt;0.05. Our preliminary data indicated APOE4 mice had a greater WT and W:L compared to APOE3. Interestingly, there were no significant differences in the remaining passive mechanical properties (LD, distensibility, stress, strain, SvS). In addition, phenylephrine and potassium-induced contractions were similar in the APOE3 and APOE4 mice. This data suggests changes in passive mechanical properties in APOE4 mice which may resemble premature aging. ABRC/ADHS18-205211 (DME, CBJ), Arizona Alzheimer’s Consortium (funded by the Arizona Department of Health Services, Contract No. CTR040636) and matching funds from Midwestern University (DME), Biomedical Sciences Program (IW, SM, DME), Biomedical Sciences Start-up Funds (DME). This is the full abstract presented at the American Physiology Summit 2024 meeting and is only available in HTML format. There are no additional versions or additional content available for this abstract. Physiology was not involved in the peer review process.

Small mesenteric artery passive mechanical properties in adult APOE3 &amp; APOE4 Mice

Previous studies from our lab have demonstrated changes in vascular structure and function in posterior cerebral arteries and left common carotid artery (CA) in adult male and female mice expressing human-ApoE targeted replacement of APOE3 (B6.129P2-Apoetm2(APOE*3)MaeN8) and APOE4 (B6.129P2-Apoetm3(APOE*4)MaeN8) (Taconic Labs). Therefore, we hypothesized that similar changes may be observed in the systemic circulation. We isolated 4thor 5th-order mesenteric arteries from adult 6-month-old male and female mice expressing hAPOE3 (n=5) or hAPOE4 (n=4). Mesenteric artery segments (5-8 mm in length) were isolated and cannulated on an arteriograph to assess vascular mechanical properties; lumen diameter, wall thickness, wall:lumen ratio, distensibility, stress versus strain (SvS), compliance, incremental modulus of elasticity (Einc), and calculated pulse wave velocity under passive conditions (Ca2+-free Krebs plus diltiazem) at intraluminal pressures ranging from 10mmHg to 140mmHg. In addition, phenylephrine-induced contraction and potassium-induced contraction were assessed using Ca2+-containing Krebs. Data was analyzed using two-way ANOVA, Student’s t-test, and analysis of nonlinear fit. Values were considered statistically different at p&lt;0.05. In our preliminary data, lumen diameter, distensibility, compliance, strain, and calculated pulse wave velocity were similar in APOE3 and APOE4 mice. Wall thickness and wall:lumen ratio were significantly greater in APOE4 compared to APOE3 mice. Wall stress and Einc were significantly less in APOE4 compared to APOE3 mice. Interestingly, the APOE4 mice exhibited a significantly lesser stress per given amount of strain compared to the APOE3 mice. Phenylephrine- and potassium-induced contractions were similar in APOE3 and APOE4 mice. This data suggests there are changes in passive mechanical properties in small mesenteric arteries from APOE4 mice, which resemble a hypertensive phenotype. ABRC/ADHS18-205211 (DME, CBJ), Arizona Alzheimer’s Consortium (funded by the Arizona Department of Health Services, Contract No. CTR040636) and matching funds from Midwestern University (DME), Biomedical Sciences Program (SM, IW, DME), Biomedical Sciences Start-up Funds (DME). This is the full abstract presented at the American Physiology Summit 2024 meeting and is only available in HTML format. There are no additional versions or additional content available for this abstract. Physiology was not involved in the peer review process.

Collagen fibers within skeletal muscle extracellular matrix dynamically change their alignment in a stretch-dependent fashion

Collagen fiber architecture within the skeletal muscle extracellular matrix (ECM) contributes to muscle passive mechanical properties. There is evidence that collagen fibers change their alignment during muscle lengthening (stretching). Thus, the goal of this study was to characterize the dynamic changes of collagen fiber alignment in the muscle ECM during muscle stretching, and to assess the relationship between dynamic collagen re-alignment and muscle passive mechanics. We hypothesized that collagen fibers increase their alignment as the muscle is stretched, and that increased collagen alignment in stretched muscle is correlated to higher elastic stiffness. Extensor digitorum longus (EDL), soleus, and diaphragm muscles were collected from wildtype (WT) and D2.mdx (MDX) mice of 48-52 weeks of age. Muscles underwent a series of twitches to determine the optimum length (Lo) for isometric contraction, and then were decellularized to isolate the muscle ECM. Decellularized muscles (DCMs) were then mechanically tested using a series of stress-relaxation tests at 5% increments from 85% to 115% length relative to Lo. Elastic stiffness was measured as the slope of the tangent line on the stress-strain curve following stress-relaxation. Following mechanical testing, DCMs were imaged using second harmonic generation microscopy to visualize collagen alignment across the range of lengths used in mechanical testing. Collagen alignment was reported as an alignment index on a scale of 0 (perfect unalignment) to 1 (perfect alignment). We found that MDX diaphragm DCMs were less stiff than WT (WT: 910.2±586.7, MDX: 238±168.7, p=0.0041), but there were no significant differences in stiffness between WT and MDX EDL and soleus DCMs. We also observed a significant effect of stretch on collagen alignment in all DCMs tested (Diaphragm: p=0.0071, EDL: p=0.0004, soleus: p&lt;0.0001). Interestingly, the collagen fibers of the epimysium, the outermost layer of the muscle ECM, were more aligned in WT diaphragm DCMs than in MDX (WT 85%: 0.672±.14, MDX 85%: 0.344±0.16, p=0.0027; WT 115%: 0.783±0.04, MDX 115%: 0.480±0.19, p=0.0036). Finally, we found a significant positive correlation between the alignment and elastic stiffness at 110% Lo across all DCMs (p=0.0038, R2=0.1713). These data indicate that collagen fibers dynamically re-align as muscle is stretched. Additionally, increased collagen fiber alignment is associated with higher passive stiffness in the decellularized muscle ECM. Overall, we find that dynamic architectural changes in the muscle ECM contribute to passive mechanical behavior during a muscle stretch. This work was supported by a grant from the NIH NIAMS (R01-AR079545). This is the full abstract presented at the American Physiology Summit 2024 meeting and is only available in HTML format. There are no additional versions or additional content available for this abstract. Physiology was not involved in the peer review process.

Defective Biomechanics and Pharmacological Rescue of Human Cardiomyocytes with Filamin C Truncations.

Actin-binding filamin C (FLNC) is expressed in cardiomyocytes, where it localizes to Z-discs, sarcolemma, and intercalated discs. Although FLNC truncation variants (FLNCtv) are an established cause of arrhythmias and heart failure, changes in biomechanical properties of cardiomyocytes are mostly unknown. Thus, we investigated the mechanical properties of human-induced pluripotent stem cells-derived cardiomyocytes (hiPSC-CMs) carrying FLNCtv. CRISPR/Cas9 genome-edited homozygous FLNCKO-/- hiPSC-CMs and heterozygous knock-out FLNCKO+/- hiPSC-CMs were analyzed and compared to wild-type FLNC (FLNCWT) hiPSC-CMs. Atomic force microscopy (AFM) was used to perform micro-indentation to evaluate passive and dynamic mechanical properties. A qualitative analysis of the beating traces showed gene dosage-dependent-manner "irregular" peak profiles in FLNCKO+/- and FLNCKO-/- hiPSC-CMs. Two Young's moduli were calculated: E1, reflecting the compression of the plasma membrane and actin cortex, and E2, including the whole cell with a cytoskeleton and nucleus. Both E1 and E2 showed decreased stiffness in mutant FLNCKO+/- and FLNCKO-/- iPSC-CMs compared to that in FLNCWT. The cell adhesion force and work of adhesion were assessed using the retraction curve of the SCFS. Mutant FLNC iPSC-CMs showed gene dosage-dependent decreases in the work of adhesion and adhesion forces from the heterozygous FLNCKO+/- to the FLNCKO-/- model compared to FLNCWT, suggesting damaged cytoskeleton and membrane structures. Finally, we investigated the effect of crenolanib on the mechanical properties of hiPSC-CMs. Crenolanib is an inhibitor of the Platelet-Derived Growth Factor Receptor α (PDGFRA) pathway which is upregulated in FLNCtv hiPSC-CMs. Crenolanib was able to partially rescue the stiffness of FLNCKO-/- hiPSC-CMs compared to control, supporting its potential therapeutic role.

The interaction of in vivo muscle operating lengths and passive stiffness in rat hindlimbs.

The operating length of a muscle is a key determinant of its ability to produce force in vivo. Muscles that operate near the peak of their force-length relationship will generate higher forces whereas muscle operating at relatively short length may be safe from sudden lengthening perturbations and subsequent damage. At longer lengths, passive mechanical properties have the potential to contribute to force or constrain operating length with stiffer muscle-tendon units theoretically being restricted to shorter lengths. Connective tissues typically increase in density during aging, thus increasing passive muscle stiffness and potentially limiting the operating lengths of muscle during locomotion. Here, we compare in vivo and in situ muscle strain from the medial gastrocnemius in young (7 months old) and aged (30-32 months old) rats presumed to have varying passive tissue stiffness to test the hypothesis that stiffer muscles operate at shorter lengths relative to their force-length relationship. We measured in vivo muscle operating length during voluntary locomotion on inclines and flat trackways and characterized the muscle force-length relationship of the medial gastrocnemius using fluoromicrometry. Although no age-related results were evident, rats of both age groups demonstrated a clear relationship between passive stiffness and in vivo operating length, such that shorter operating lengths were significantly correlated with greater passive stiffness. Our results suggest that increased passive stiffness may restrict muscles to operating lengths shorter than optimal lengths, potentially limiting force capacity during locomotion.

Variability of intervertebral joint stiffness between specimens and spine levels.

Introduction: Musculoskeletal multibody models of the spine can be used to investigate the biomechanical behaviour of the spine. In this context, a correct characterisation of the passive mechanical properties of the intervertebral joint is crucial. The intervertebral joint stiffness, in particular, is typically derived from the literature, and the differences between individuals and spine levels are often disregarded. Methods: This study tested if an optimisation method of personalising the intervertebral joint stiffnesses was able to capture expected stiffness variation between specimens and between spine levels and if the variation between spine levels could be accurately captured using a generic scaling ratio. Multibody models of six T12 to sacrum spine specimens were created from computed tomography data. For each specimen, two models were created: one with uniform stiffnesses across spine levels, and one accounting for level dependency. Three loading conditions were simulated. The initial stiffness values were optimised to minimize the kinematic error. Results: There was a range of optimised stiffnesses across the specimens and the models with level dependent stiffnesses were less accurate than the models without. Using an optimised stiffness substantially reduced prediction errors. Discussion: The optimisation captured the expected variation between specimens, and the prediction errors demonstrated the importance of accounting for level dependency. The inaccuracy of the predicted kinematics for the level-dependent models indicated that a generic scaling ratio is not a suitable method to account for the level dependency. The variation in the optimised stiffnesses for the different loading conditions indicates personalised stiffnesses should also be considered load-specific.

Impact of knockout of dual-specificity protein phosphatase 5 on structural and mechanical properties of rat middle cerebral arteries: implications for vascular aging.

Vascular aging influences hemodynamics, elevating risks for vascular diseases and dementia. We recently demonstrated that knockout (KO) of Dusp5 enhances cerebral and renal hemodynamics and cognitive function. This improvement correlates with elevated pPKC and pERK1/2 levels in the brain and kidneys. Additionally, we observed that Dusp5 KO modulates the passive mechanical properties of cerebral and renal arterioles, associated with increased myogenic tone at low pressure, enhanced distensibility, greater compliance, and reduced stiffness. The present study evaluates the structural and mechanical properties of the middle cerebral artery (MCA) in Dusp5 KO rats. We found that vascular smooth muscle cell layers and the collagen content in the MCA wall are comparable between Dusp5 KO and control rats. The internal elastic lamina in the MCA of Dusp5 KO rats exhibits increased thickness, higher autofluorescence intensity, smaller fenestrae areas, and fewer fenestrations. Despite an enhanced myogenic response and tone of the MCA in Dusp5 KO rats, other passive mechanical properties, such as wall thickness, cross-sectional area, wall-to-lumen ratio, distensibility, incremental elasticity, circumferential wall stress, and elastic modulus, do not significantly differ between strains. These findings suggest that while Dusp5 KO has a limited impact on altering the structural and mechanical properties of MCA, its primary role in ameliorating hemodynamics and cognitive functions is likely attributable to its enzymatic activity on cerebral arterioles. Further research is needed to elucidate the specific enzymatic mechanisms and explore potential clinical applications in the context of vascular aging.

Numerical modeling of the abdominal wall biomechanics and experimental analysis for model validation.

The evaluation of the biomechanics of the abdominal wall is particularly important to understand the onset of pathological conditions related to weakening and injury of the abdominal muscles. A better understanding of the biomechanics of the abdominal wall could be a breakthrough in the development of new therapeutic approaches. For this purpose, several studies in the literature propose finite element models of the human abdomen, based on the geometry of the abdominal wall from medical images and on constitutive formulations describing the mechanical behavior of fascial and muscular tissues. The biomechanics of the abdominal wall depends on the passive mechanical properties of fascial and muscle tissue, on the activation of abdominal muscles, and on the variable intra-abdominal pressure. To assess the quantitative contribution of these features to the development and validation of reliable numerical models, experimental data are fundamental. This work presents a review of the state of the art of numerical models developed to investigate abdominal wall biomechanics. Different experimental techniques, which can provide data for model validation, are also presented. These include electromyography, ultrasound imaging, intraabdominal pressure measurements, abdominal surface deformation, and stiffness/compliance measurements.

Mechanical characteristics of the ureter and clinical implications.

The ureteric wall is a complex multi-layered structure. The ureter shows variation in passive mechanical properties, histological morphology and insertion forces along the anatomical length. Ureter mechanical properties also vary depending on the direction of tensile testing and the anatomical region tested. Compliance is greatest in the proximal ureter and lower in the distal ureter, which contributes to the role of the ureter as a high-resistance sphincter. Similar to other human tissues, the ureteric wall remodels with age, resulting in changes to the mechanical properties. The passive mechanical properties of the ureter vary between species, and variation in tissue storage and testing methods limits comparison across some studies. Knowledge of the morphological and mechanical properties of the ureteric wall can aid in understanding urine transport and safety thresholds in surgical techniques. Indeed, various factors alter the forces required to insert access sheaths or scopes into the ureter, including sheath diameter, safety wires and medications. Future studies on human ureteric tissue both in vivo and ex vivo are required to understand the mechanical properties of the ureter and how forces influence these properties. Testing of instrument insertion forces in humans with a focus on defining safe upper limits and techniques to reduce trauma are also needed. Last, evaluation of dilatation limits in the mid and proximal ureter and clarification of tensile strength anisotropy in human specimens are necessary.

Multiscale analysis of Klf10's impact on the passive mechanical properties of murine skeletal muscle

Skeletal muscle is a hierarchical structure composed of multiple organizational scales. A major challenge in the biomechanical evaluation of muscle relates to the difficulty in evaluating the experimental mechanical properties at the different organizational levels of the same tissue. Indeed, the ability to integrate mechanical properties evaluated at various levels will allow for improved assessment of the entire tissue, leading to a better understanding of how changes at each level evolve over time and/or impact tissue function, especially in the case of muscle diseases.Therefore, the purpose of this study was to analyze a genetically engineered mouse model (Klf10 KO: Krüppel-Like Factor 10 knockout) with known skeletal muscle defects to compare the mechanical properties with wild-type (WT) controls at the three main muscle scales: the macroscopic (whole muscle), microscopic (fiber) and submicron (myofibril) levels. Passive mechanical tests (ramp, relaxation) were performed on two types of skeletal muscle (soleus and extensor digitorum longus (EDL)).Results of the present study revealed muscle-type specific behaviors in both genotypes only at the microscopic scale. Interestingly, loss of Klf10 expression resulted in increased passive properties in the soleus but decreased passive properties in the EDL compared to WT controls.At the submicron scale, no changes were observed between WT and Klf10 KO myofibrils for either muscle; these results demonstrate that the passive property differences observed at the microscopic scale (fiber) are not caused by sarcomere intrinsic alterations but instead must originate outside the sarcomeres, likely in the collagen-based extracellular matrix. The macroscopic scale revealed similar passive mechanical properties between WT and Klf10 KO hindlimb muscles.The present study has allowed for a better understanding of the role of Klf10 on the passive mechanical properties of skeletal muscle and has provided reference data to the literature which could be used by the community for muscle multiscale modeling.

Mechanomics study of cardiomyocytes with filamin c truncations

Abstract Background Filamin C (FLNC) is expressed in cardiomyocytes, where it binds to actin and localizes to Z-discs, sarcolemma, and intercalated discs. Although FLNC truncation variants (FLNCtv) are an established cause of arrhythmias and heart failure (arrhythmogenic cardiomyopathy), the underlying mechanisms, in particular changes in mechanical properties of cardiomyocytes, are mostly unknown. Purpose In this study, we applied a biophysical approach to investigate the interaction between altered mechanical properties and biological response in human induced pluripotent stem cells–derived cardiomyocytes (hiPSC-CMs) carrying FLNCtv. Methods CRISPR/Cas9 genome-edited FLNC-/- hiPSC-CMs, a homozygous condition that is lethal in animal models, and FLNC+/- hiPSC-CMs, recapitulating the heterozygous human disease, were analyzed. Wild-type FLNC hiPSC-CMs were used as controls. Atomic Force microscopy (AFM) was used to perform single-cell force spectroscopy (SCFS) microindentation, to evaluate passive and dynamic mechanical properties. From the loading curves, two cell Young’s Moduli were calculated: E1, related to the compression of the plasma membrane and actin cortex, and E2, including the rest of the inner cell layers (cytoskeleton and nucleus). Cell adhesion was assessed using the retraction curve of the SCFS. Data were processed in terms of adhesion force (the highest value of the force exerted by the cell-surface contact to the cantilever during retraction) and work of adhesion (integrating the area under the retraction curve). Finally, FLNC-/- hiPSC-CMs were incubated with 1 µM Crenolanib (a PDGFRA signaling inhibitor) for 3 days, and the microindentation was performed again using DMSO-only-treated FLNC-/- cells as controls. Results The AFM indentation curve for the cells analyzed showed significant differences. Both elastic contributions (E1 and E2) show that wild-type FLNC iPSC-CMs are stiffer than both mutant FLNC+/- and FLNC-/- iPSC-CMs (see Figure upper panel). The adhesion showed the same trend as the elasticity: mutant FLNC iPSC-CMs showed a progressive decrease of work of adhesion as well as max adhesion force from the FLNC+/- to the FLNC-/- models. Rescue of the latter with Crenolanib showed to moderately increase their stiffness. Moreover, a qualitative analysis of the beating traces showed that FLNC+/- but mostly FLNC-/- display "irregular" small peaks, resembling those of delayed after depolarizations (see Figure lower panel). Conclusions We found that FLNCtv causes a decrease in cell stiffness which declines progressively from the heterozygous status, which is associated with FLNC haploinsufficiency, to the homozygous status, which lacks FLNC. This indicates a progressive softening of the cardiomyocytes, suggesting a damaged cytoskeleton. Crenolanib rescue suggests that the inhibition of PDGFRA signaling could partially restore such damage (see Figure upper panel - right corner).

Abstract 16749: Influence of Dual-Specificity Protein Phosphatase 5 on Structural and Mechanical Properties of Rat Middle Cerebral Artery

Dual-specificity protein phosphatase 5 (DUSP5) is a multifunctional phosphatase that modulates signaling cascades by catalyzing the dephosphorylation of both threonine and tyrosine residues. We recently reported that KO of Dusp5 enhances cerebral and renal hemodynamics and cognitive function. This effect is associated with increased pPKC and pERK1/2 levels in arteries and arterioles of the brain and kidneys. Further, we found that KO of Dusp5 contributes to the regulation of arteriolar passive mechanical properties with higher myogenic tones, better distensibility, greater compliance, and less stiffness. The present study focuses on the structural and mechanical properties of rat middle cerebral artery (MCA) to evaluate whether it contributes to enhanced vascular and cognitive function in Dusp5 KO rats. Vascular smooth muscle cell layer numbers and collagen content in the wall of the MCA are similar in Dusp5 KO and control rats. While external elastic lamina was absent in the MCA in both strains, internal elastic lamina was thicker in the MCA of Dusp5 KO vs. control rats (2.33 ± 0.02 vs. 1.85 ± 0.03 μm) and associated with higher autofluorescence intensity (953.76 ± 10.03 vs. 737.31 ± 64.88 au), smaller fenestrae areas (51.31 ± 3.62 vs. 70.46 ± 2.24), and fewer number of fenestrations (138.19 ± 8.86 vs. 374.73 ± 17.02 μm 2 ). Even though the myogenic tone is enhanced in Dusp5 KO vs. control rats (52.37 ± 1.65 vs. 44.87 ± 2.00%), other passive mechanical properties (wall thickness, cross-sectional area, wall-to-lumen ratio, wall tension, distensibility, incremental distensibility, circumferential wall strain, circumferential wall stress, and elastin modulus) of the MCA of Dusp5 KO rats do not exhibit significant changes. The findings suggest that while Dusp5 KO has a limited impact on changing the structural and mechanical properties of the MCA, its role in enhancing hemodynamics and cognitive function is primarily attributed to its enzymatic function.

The immediate effect of multidirectional elastic tape on the passive mechanical properties of the ankle joint

The immediate effect of multidirectional elastic tape on the passive mechanical properties of the ankle joint