51 research outputs found

    Numerical Simulation in Aortic Arch Aneurysm

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    Stress analysis in a layered aortic arch model under pulsatile blood flow

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    BACKGROUND: Many cardiovascular diseases, such as aortic dissection, frequently occur on the aortic arch and fluid-structure interactions play an important role in the cardiovascular system. Mechanical stress is crucial in the functioning of the cardiovascular system; therefore, stress analysis is a useful tool for understanding vascular pathophysiology. The present study is concerned with the stress distribution in a layered aortic arch model with interaction between pulsatile flow and the wall of the blood vessel. METHODS: A three-dimensional (3D) layered aortic arch model was constructed based on the aortic wall structure and arch shape. The complex mechanical interaction between pulsatile blood flow and wall dynamics in the aortic arch model was simulated by means of computational loose coupling fluid-structure interaction analyses. RESULTS: The results showed the variations of mechanical stress along the outer wall of the arch during the cardiac cycle. Variations of circumferential stress are very similar to variations of pressure. Composite stress in the aortic wall plane is high at the ascending portion of the arch and along the top of the arch, and is higher in the media than in the intima and adventitia across the wall thickness. CONCLUSION: Our analysis indicates that circumferential stress in the aortic wall is directly associated with blood pressure, supporting the clinical importance of blood pressure control. High stress in the aortic wall could be a risk factor in aortic dissections. Our numerical layered aortic model may prove useful for biomechanical analyses and for studying the pathogeneses of aortic dissection

    Farnesyl pyrophosphate regulates adipocyte functions as an endogenous PPARγ agonist

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    The cholesterol biosynthetic pathway produces not only sterols but also non-sterol mevalonate metabolites involved in isoprenoid synthesis. Mevalonate metabolites affect transcriptional and post-transcriptional events that in turn affect various biological processes including energy metabolism. In the present study, we examine whether mevalonate metabolites activate PPARγ (peroxisome-proliferator-activated receptor γ), a ligand-dependent transcription factor playing a central role in adipocyte differentiation. In the luciferase reporter assay using both GAL4 chimaera and full-length PPARγ systems, a mevalonate metabolite, FPP (farnesyl pyrophosphate), which is the precursor of almost all isoprenoids and is positioned at branch points leading to the synthesis of other longer-chain isoprenoids, activated PPARγ in a dose-dependent manner. FPP induced the in vitro binding of a co-activator, SRC-1 (steroid receptor co-activator-1), to GST (glutathione transferase)–PPARγ. Direct binding of FPP to PPARγ was also indicated by docking simulation studies. Moreover, the addition of FPP up-regulated the mRNA expression levels of PPARγ target genes during adipocyte differentiation induction. In the presence of lovastatin, an HMG-CoA (3-hydroxy-3-methylglutaryl-CoA) reductase inhibitor, both intracellular FPP levels and PPARγ-target gene expressions were decreased. In contrast, the increase in intracellular FPP level after the addition of zaragozic acid, a squalene synthase inhibitor, induced PPARγ-target gene expression. The addition of FPP and zaragozic acid promotes lipid accumulation during adipocyte differentiation. These findings indicated that FPP might function as an endogenous PPARγ agonist and regulate gene expression in adipocytes

    Geographical Distribution of Meloidogyne Species (Nematoda: Tylenchida) in Tobacco Fields of Japan

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    Asynchronous Island Parallel GA Using Multiform Subpopulations

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    . Island Parallel GA divides a population into subpopulations and assigns them to processing elements on a parallel computer. Then each subpopulation searches the optimal solution independently, and exchanges individuals periodically. This exchange operation is called migration. In this research, we propose a new algorithm that migrants are exchanged asynchronously among multiform subpopulations which have different search conditions. The effect of our algorithm on combinational optimization problems was verified by applying the algorithm to Knapsack Problem and Royal Road Functions using parallel computer CRAY-T3E. We obtained the results that our algorithm maintained the population's diversity effectively and searches building blocks efficiently. 1 Introduction There are two typical problems in Genetic Algorithms (GAs). First, GAs require huge calculation time for their genetic operations, such as selection, crossover, mutation, and individuals' fitness evaluations. Secondly, mainten..

    Blood Flow Simulation System with Interaction between Blood Flow and Blood Vessel Wall using Image Based Cartesian Grid

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    For the simulation of the fluid-structure interaction (FSI) between the blood flow and blood vessel walls, we have examined the voxel-based FSI method. This method uses a Cartesian grid, called voxel, made from medical images. Further, we have tested the accuracy and reliability of this simple method and have observed its features. In this document, we discuss the background, kinetic models of the blood vessel, a numerical method, and the result of an experiment conducted using an artificial identical shape and an actual realistic shape
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