241 research outputs found

    Secure data aggregation in wireless sensor networks: A survey

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    Data aggregation is a widely used technique in wireless sensor networks. The security issues, data confidentiality and integrity, in data aggregation become vital when the sensor network is deployed in a hostile environment. There has been many related work proposed to address these security issues. In this paper we survey these work and classify them into two cases: hop-by-hop encrypted data aggregation and end-to-end encrypted data aggregation. We also propose two general frameworks for the two cases respectively. The framework for end-to-end encrypted data aggregation has higher computation cost on the sensor nodes, but achieves stronger security, in comparison with the framework for hop-by-hop encrypted data aggregation.Yingpeng Sang, Hong Shen, Yasushi Inoguchi, Yasuo Tan, Naixue Xion

    Explicit solutions to the semi-discrete modified KdV equation and motion of discrete plane curves

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    We construct explicit solutions to continuous motion of discrete plane curves described by a semi-discrete potential modified KdV equation. Explicit formulas in terms the Ļ„\tau function are presented. B\"acklund transformations of the discrete curves are also discussed. We finally consider the continuous limit of discrete motion of discrete plane curves described by the discrete potential modified KdV equation to motion of smooth plane curves characterized by the potential modified KdV equation

    Discrete Integrable Systems and Hodograph Transformations Arising from Motions of Discrete Plane Curves

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    We consider integrable discretizations of some soliton equations associated with the motions of plane curves: the Wadati-Konno-Ichikawa elastic beam equation, the complex Dym equation, and the short pulse equation. They are related to the modified KdV or the sine-Gordon equations by the hodograph transformations. Based on the observation that the hodograph transformations are regarded as the Euler-Lagrange transformations of the curve motions, we construct the discrete analogues of the hodograph transformations, which yield integrable discretizations of those soliton equations.Comment: 19 page

    Improvements in vascular health by a low-fat diet, but not a high-fat diet, are mediated by changes in adipocyte biology

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    <p>Abstract</p> <p>Background</p> <p>Low-fat (LF) and high-fat (HF) weight loss diets improve brachial artery flow-mediated dilation (FMD) in obese individuals, although results are conflicting. Moreover, the role that adipose tissue plays in mediating these diet-related effects are unknown.</p> <p>Objective</p> <p>This study examined how modulations in FMD by HF and LF diets relate to changes in adipocyte parameters.</p> <p>Design</p> <p>Obese subjects (n = 17) were randomized to a HF diet (60% kcal as fat) or a LF diet (25% kcal as fat) for 6 weeks. Both groups were restricted by 25% of energy needs.</p> <p>Results</p> <p>Body weight decreased (<it>P <</it>0.05) in both groups (HF: -6.6 Ā± 0.5 kg, LF: -4.7 Ā± 0.6 kg). Fat mass and waist circumference were reduced (<it>P <</it>0.05) in the LF group only (-4.4 Ā± 0.3 kg; -3.6 Ā± 0.8 cm, respectively). FMD improved (<it>P <</it>0.05) in the LF group (7.4 Ā± 0.8% to 9.8 Ā± 0.8; 32% increase) and was impaired in the HF group (8.5 Ā± 0.6% to 6.9 Ā± 0.7; 19% reduction). Increases in plasma adiponectin (<it>P <</it>0.05, 16 Ā± 5%), and decreases in resistin (<it>P <</it>0.05, -26 Ā± 11%), were shown by the LF diet only. Greater decreases in leptin were observed with LF (-48 Ā± 9%) versus HF (-28 Ā± 12%) (<it>P <</it>0.05, diet Ɨ time). Increased FMD by the LF diet was associated with increased adiponectin, and decreased fat mass, waist circumference, leptin, and resistin.</p> <p>Conclusion</p> <p>Beneficial modulations in vascular health by LF diets may be mediated by improvements in adipocyte parameters.</p

    Lagrangian Curves in a 4-dimensional affine symplectic space

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    Lagrangian curves in R4 entertain intriguing relationships with second order deformation of plane curves under the special affine group and null curves in a 3-dimensional Lorentzian space form. We provide a natural affine symplectic frame for Lagrangian curves. It allows us to classify La- grangrian curves with constant symplectic curvatures, to construct a class of Lagrangian tori in R4 and determine Lagrangian geodesic

    Mind the gap: connexins and cellā€“cell communication in the diabetic kidney

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    Connexins, assembled as a hexameric connexon, form a transmembrane hemichannel that provides a conduit for paracrine signalling of small molecules and ions to regulate the activity and function of adjacent cells. When hemichannels align and associate with similar channels on opposing cells, they form a continuous aqueous pore or gap junction, allowing the direct transmission of metabolic and electrical signals between coupled cells. Regulation of gap junction synthesis and channel activity is critical for cell function, and a number of diseases can be attributed to changes in the expression/function of these important proteins. Diabetic nephropathy is associated with several complex metabolic and inflammatory responses characterised by defects at the molecular, cellular and tissue level. In both type 1 and type 2 diabetes, glycaemic injury of the kidney is the leading cause of end-stage renal failure, a consequence of multiple aetiologies, including increased deposition of extracellular matrix, glomerular hyperfiltration, albuminuria and tubulointerstitial fibrosis. In diabetic nephropathy, loss of connexin mediated cellā€“cell communication within the nephron may represent an early sign of disease; however, our current knowledge of the role of connexins in the diabetic kidney is sparse. This review highlights recent evidence demonstrating that maintenance of connexin-mediated cellā€“cell communication could benefit region-specific renal function in diabetic nephropathy and suggests that these proteins should be viewed as a tantalising novel target for therapeutic intervention

    Investigating the Role of Islet Cytoarchitecture in Its Oscillation Using a New Ī²-Cell Cluster Model

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    The oscillatory insulin release is fundamental to normal glycemic control. The basis of the oscillation is the intercellular coupling and bursting synchronization of Ī² cells in each islet. The functional role of islet Ī² cell mass organization with respect to its oscillatory bursting is not well understood. This is of special interest in view of the recent finding of islet cytoarchitectural differences between human and animal models. In this study we developed a new hexagonal closest packing (HCP) cell cluster model. The model captures more accurately the real islet cell organization than the simple cubic packing (SCP) cluster that is conventionally used. Using our new model we investigated the functional characteristics of Ī²-cell clusters, including the fraction of cells able to burst fb, the synchronization index Ī» of the bursting Ī² cells, the bursting period Tb, the plateau fraction pf, and the amplitude of intracellular calcium oscillation [Ca]. We determined their dependence on cluster architectural parameters including number of cells nĪ², number of inter-Ī² cell couplings of each Ī² cell nc, and the coupling strength gc. We found that at low values of nĪ², nc and gc, the oscillation regularity improves with their increasing values. This functional gain plateaus around their physiological values in real islets, at nĪ²āˆ¼100, ncāˆ¼6 and gcāˆ¼200 pS. In addition, normal Ī²-cell clusters are robust against significant perturbation to their architecture, including the presence of non-Ī² cells or dead Ī² cells. In clusters with nĪ²>āˆ¼100, coordinated Ī²-cell bursting can be maintained at up to 70% of Ī²-cell loss, which is consistent with laboratory and clinical findings of islets. Our results suggest that the bursting characteristics of a Ī²-cell cluster depend quantitatively on its architecture in a non-linear fashion. These findings are important to understand the islet bursting phenomenon and the regulation of insulin secretion, under both physiological and pathological conditions
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