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High strain rate compression of soft tissues has recently gained attention due to its application in computational simulation of traumatic injuries. To understand high rate tissue behavior, a comparative study is needed to examine the biomechanical responses of multiple soft tissues. We hypothesized that the underlying mechanisms of soft tissue high rate compression is dependent upon water, microstructural organization, and extracellular matrix (ECM). Porcine brain, liver, and tendon, which have similar material density (brain: 1.05g/cm³, liver: 1.06g/cm³, and tendon: 1.12g/cm³) and water content (brain: $\sim$78%, liver: $\sim$71–75%, and tendon: $\sim$70%) but different cellularity and ECM properties, were subjected to polymeric split Hopkinson pressure bar (PSHPB) testing. Hydrated brain tissue, due to its high microstructural cavities (cavity area $\mathrm{\text{fraction}}=0.49\pm 0.26$) and low ECM content, had a high initial stress spike of $0.22\pm 0.12$MPa. Hydrated liver, with moderate microstructural cavities (cavity area $\mathrm{\text{fraction}}=0.30\pm 0.07$) and moderate ECM content, had a moderate stress spike of $0.10\pm 0.04$MPa. Hydrated tendon had low microstructural cavities (cavity area $\mathrm{\text{fraction}}=0.03\pm 0.02$) and high ECM content and had a minimal initial stress spike of $0.02\pm 0.01$MPa. Electron microscopy of the tissues’ microstructural cavities revealed a first-order estimation of water content that was not bound to ECM (e.g., intracellular water). Linear regression analysis showed that the initial spike was highly correlated ($r^2=0.9532$) with intracellular water. To understand the role of water in each tissue’s response to high deformation, each soft tissue was completely dehydrated and subjected to the same PSHPB compression test. After removal of all the water, neither the brain, liver, nor tendon revealed an initial stress spike, implicating the essential nature of water in the initial responses of high-rate compression. These results suggest that cellular water and ECM content play a critical role in the biomechanical responses to high strain rate compression.

Momordica charantia (MC) is a plant belonging to the family Cucurbitaceae. MC has antidiabetic, antibacterial, antioxidant, antimutagenic, antiulcerative, antiinflammatory and antilipidemic effects. However, information on the effect of MC on fracture union is lacking. This study aimed to examine the effect of MC on fracture union histopathologically and biomechanically. A total of 42 male Wistar-Albino rats were randomly divided into 3 groups, 14 in each group. A diaphyseal fracture was created on the right tibia of all rats. All fractures were fixed with a Kirschner (K) wire. The rats in Group I did not undergo any further procedures (Control group). Group II rats were treated with 0.9% saline oral gavage at a dose of $500\mu$L/day for 28 days [Saline (S) group]. The rats in Group III were given 300mg/kg MC extract per day, dissolved in $500\mu$L 0.9% saline by oral gavage for 28 days [MC (Extract) group]. After 28 days, all rats were sacrificed. Each group was randomly divided into two subgroups. The histopathological examination was performed on the right tibia of rats in the first subgroup and the biomechanical examination in the second subgroup. The kidneys and livers of all rats were evaluated histopathologically. Fracture union was significantly better in the Extract group compared with the Control and S groups histopathologically. The fracture inflammation values were lower in the Extract group than in the other groups. No statistically significant difference was found between the groups in terms of possible side effects to kidneys and livers. In terms of biomechanics, fracture union was significantly better in the Extract group compared with the Control and S groups except yield displacement values. MC had a positive effect on fracture union histopathologically and biomechanically.

Hepatic injury induced by blunt abdominal impact is a major cause of death in vehicle crashes. However, few works have been done effectively in cadaver experiments to clarify the liver’s specific dynamic behavior and mechanical characteristics. This paper described the dynamic behavior and mechanical characteristics of the liver under blunt impacts to the upper abdomen with the finite element model (FEM) of the Chinese human body — the 50 percentile-sized male (CHUBM-M50). The simulation matrix, three directions (frontal, oblique, lateral), and four speeds included in each group were designed with a 23.4kg, rigid cylindrical impactor aligning the T11 level. The liver deformation contours displayed compression against the spine and rotation in the horizontal plane, which were the two main features in liver motion. Pressure distribution in the liver capsule and parenchyma was discussed to elucidate the biomechanical characteristics related to impact direction. Generally, the stress distribution in the capsule was 10 times higher than that in the parenchyma. A discussion of the injury mechanism of the liver capsule and parenchyma observed in the simulations was given upon the pressure distribution. It demonstrated that the capsule could protect liver parenchyma at low-speed impacts and should not be neglected for understanding liver injury mechanisms.