Vertex Displacement-Based Discontinuous Deformation Analysis Using Virtual Element Method.

To avoid disadvantages caused by rotational degrees of freedom in the original Discontinuous Deformation Analysis (DDA), a new block displacement mode is defined within a time step, where displacements of all the block vertices are taken as the degrees of freedom. An individual virtual element space V1(Ω) is defined for a block to illustrate displacement of the block using the Virtual Element Method (VEM). Based on VEM theory, the total potential energy of the block system in DDA is formulated and minimized to obtain the global equilibrium equations. At the end of a time step, the vertex coordinates are updated by adding their incremental displacement to their previous coordinates. In the new method, no explicit expression for the displacement u is required, and all numerical integrations can be easily computed. Four numerical examples originally designed by Shi are analyzed, verifying the effectiveness and precision of the proposed method.

Modeling Structural Dynamics Using FE-Meshfree QUAD4 Element with Radial-Polynomial Basis Functions.

The PU (partition-of-unity) based FE-RPIM QUAD4 (4-node quadrilateral) element was proposed for statics problems. In this element, hybrid shape functions are constructed through multiplying QUAD4 shape function with radial point interpolation method (RPIM). In the present work, the FE-RPIM QUAD4 element is further applied for structural dynamics. Numerical examples regarding to free and forced vibration analyses are presented. The numerical results show that: (1) If CMM (consistent mass matrix) is employed, the FE-RPIM QUAD4 element has better performance than QUAD4 element under both regular and distorted meshes; (2) The DLMM (diagonally lumped mass matrix) can supersede the CMM in the context of the FE-RPIM QUAD4 element even for the scheme of implicit time integration.

Ubiquinol-10 supplementation activates mitochondria functions to decelerate senescence in senescence-accelerated mice.

AIM: The present study was conducted to define the relationship between the anti-aging effect of ubiquinol-10 supplementation and mitochondrial activation in senescence-accelerated mouse prone 1 (SAMP1) mice. RESULTS: Here, we report that dietary supplementation with ubiquinol-10 prevents age-related decreases in the expression of sirtuin gene family members, which results in the activation of peroxisome proliferator-activated receptor γ coactivator 1α (PGC-1α), a major factor that controls mitochondrial biogenesis and respiration, as well as superoxide dismutase 2 (SOD2) and isocitrate dehydrogenase 2 (IDH2), which are major mitochondrial antioxidant enzymes. Ubiquinol-10 supplementation can also increase mitochondrial complex I activity and decrease levels of oxidative stress markers, including protein carbonyls, apurinic/apyrimidinic sites, malondialdehydes, and increase the reduced glutathione/oxidized glutathione ratio. Furthermore, ubiquinol-10 may activate Sirt1 and PGC-1α by increasing cyclic adenosine monophosphate (cAMP) levels that, in turn, activate cAMP response element-binding protein (CREB) and AMP-activated protein kinase (AMPK). INNOVATION AND CONCLUSION: These results show that ubiquinol-10 may enhance mitochondrial activity by increasing levels of SIRT1, PGC-1α, and SIRT3 that slow the rate of age-related hearing loss and protect against the progression of aging and symptoms of age-related diseases.