The Influence of Finite Element Meshing Accuracy on a Welding Machine for Offshore Platform’S Modal Analysis

The purpose objective of this study was to investigate the influence of finite element meshing accuracy on modal analysis which is one of the basic factors affecting the accuracy of finite element analysis and mostly preoccupies the working staff in pre-processing finite element simulation models. In this paper, we established several finite element models of a welding machine for offshore platform, with the meshing accuracy as the variable and workbench software as the platform for modal analysis, as the same time, comparing the analysis results. The results indicated that for some specific structures and simulation types, mesh refinement alone does not achieve desired results, and the authors indicate that mesh refinement is rarely related to the equipment’s low-frequency modal analysis but it’s great related to the equipment’s high-frequency modal analysis. The findings of this study may serve as breaking the opinion that smaller mesh size means higher calculation precision and provides references for mesh division practices in low frequency modal analysis

Diminished α7 nicotinic acetylcholine receptor (α7nAChR) rescues amyloid-β induced atrial remodeling by oxi-CaMKII/MAPK/AP-1 axis-mediated mitochondrial oxidative stress

The potential coexistence of Alzheimer's disease (AD) and atrial fibrillation (AF) is increasingly common as aging-related diseases. However, little is known about mechanisms responsible for atrial remodeling in AD pathogenesis. α7 nicotinic acetylcholine receptors (α7nAChR) has been shown to have profound effects on mitochondrial oxidative stress in both organ diseases. Here, we investigate the role of α7nAChR in mediating the effects of amyloid-β (Aβ) in cultured mouse atrial cardiomyocytes (HL-1 cells) and AD model mice (APP/PS1). In vitro, apoptosis, oxidative stress and mitochondrial dysfunction induced by Aβ long-term (72h) in HL-1 cells were prevented by α-Bungarotoxin(α-BTX), an antagonist of α7nAChR. This cardioprotective effect was due to reinstating Ca2+ mishandling by decreasing the activation of CaMKII and MAPK signaling pathway, especially the oxidation of CaMKII (oxi-CaMKII). In vivo studies demonstrated that targeting knockdown of α7nAChR in cardiomyocytes could ameliorate AF progression in late-stage (12 months) APP/PS1 mice. Moreover, α7nAChR deficiency in cardiomyocytes attenuated APP/PS1-mutant induced atrial remodeling characterized by reducing fibrosis, atrial dilation, conduction dysfunction, and inflammatory mediator activities via suppressing oxi-CaMKII/MAPK/AP-1. Taken together, our findings suggest that diminished α7nAChR could rescue Aβ-induced atrial remodeling through oxi-CaMKII/MAPK/AP-1-mediated mitochondrial oxidative stress in atrial cells and AD mice