In vivo formation of 8-Epi-prostaglandin F2 alpha is increased in hypercholesterolemia

F2-isoprostanes are bioactive prostaglandin (PG)-like compounds that are produced from arachidonic acid through a nonenzymatic process of lipid peroxidation catalyzed by oxygen free-radicals. 8-Epi-PGF2 alpha may amplify the platelet response to agonists, circulates in plasma, and is excreted in urine. We examined the hypothesis that the formation of 8-epi-PGF2 alpha is altered in patients with hypercholesterolemia and contributes to platelet activation in this setting. Urine samples were obtained from 40 hypercholesterolemic patients and 40 age- and sex-matched control subjects for measurement of immunoreactive 8-epi-PGF2 alpha. Urinary excretion of 11-dehydro-thromboxane (TX) B2, a major metabolite of TXA2, was measured as an in vivo index of platelet activation. Low-dose aspirin, indobufen, and vitamin E were used to investigate the mechanism of formation and effects of 8-epi-PGF2 alpha on platelet activation. Urinary 8-epi-PGF2 alpha was significantly (P = .0001) higher in hypercholesterolemic patients than in control subjects: 473 +/- 305 versus 205 +/- 95 pg/mg creatinine. Its rate of excretion was inversely related to the vitamin E content of LDL and showed a positive correlation with urinary 11-dehydro-TXB2. Urinary 8-epi-PGF2 alpha was unchanged after 2-week dosing with aspirin and indobufen despite complete suppression of TX metabolite excretion. Vitamin E supplementation was associated with dose-dependent reductions in both urinary 8-epi-PGF2 alpha and 11-dehydro-TXB2 by 34% to 36% and 47% to 58% at 100 and 600 mg daily, respectively. We conclude that the in vivo formation of the F2-isoprostane 8-epi-PGF2 alpha is enhanced in the vast majority of patients with hypercholesterolemia. This provides an aspirin-insensitive mechanism possibly linking lipid peroxidation to amplification of platelet activation in the setting of hypercholesterolemia. Dose-dependent suppression of enhanced 8-epi-PGF2 alpha formation by vitamin E supplementation may contribute to the beneficial effects of antioxidant treatment.     

Robust stability and stabilization of uncertain linear positive systems via integral linear constraints: L1‐gain and L∞‐gain characterization

Copositive linear Lyapunov functions are used along with dissipativity theory for stability analysis and control of uncertain linear positive systems. Unlike usual results on linear systems, linear supply rates are employed here for robustness and performance analysis using L₁‐gain and L_∞‐gain. Robust stability analysis is performed using integral linear constraints for which several classes of uncertainties are discussed. The approach is then extended to robust stabilization and performance optimization. The obtained results are expressed in terms of robust linear programming problems that are equivalently turned into finite dimensional ones using Handelman's theorem. Several examples are provided for illustration. Copyright © 2012 John Wiley & Sons, Ltd.     

Model of Frequency Analysis in the Visual Cortex and the Shape from Texture Problem

This paper addresses the question: at the level of cortical cells present in the primary area V1, is the information sufficient to extract the local perspective from the texture? Starting from a model of complex cells in visual area V1, we propose a biologically plausible algorithm for frequency analysis applied to the shape from texture problem. First, specific log-normal filters are designed in replacement of the classical Gabor filters because of their theoretical properties and of their biological plausibility. These filters are separable in frequency and orientation and they better sample the image spectrum which makes them appropriate for any pattern analysis technique. A method to estimate the local frequency in the image, which discards the need to choose the best local scale, is designed. Based on this frequency analysis model, a local decomposition of the image into patches leads to the estimation of the local frequency variation which is used to solve the problem of recovering the shape from the texture. From the analytical relation between the local frequency and the geometrical parameters, under perspective projection, it is possible to recover the orientation and the shape of the original image. The accuracy of the method is evaluated and discussed on different kind of textures, both regular and irregular, with planar and curved surfaces and also on natural scenes and psychophysical stimuli. It compares favorably to the best existing methods, with in addition, a low computational cost. The biological plausibility of the model is finally discussed.     

12.1‐in. WXGA AMOLED display driven by InGaZnO thin‐film transistors

Abstract— A full‐color 12.1‐in.WXGA active‐matrix organic‐light‐emitting‐diode (AMOLED) display was, for the first time, demonstrated using indium‐gallium‐zinc oxide (IGZO) thin‐film transistors (TFTs) as an active‐matrix backplane. It was found that the fabricated AMOLED display did not suffer from the well‐known pixel non‐uniformity in luminance, even though the simple structure consisting of two transistors and one capacitor was adopted as the unit pixel circuit, which was attributed to the amorphous nature of IGZO semiconductors. The n‐channel a‐IGZO TFTs exhibited a field‐effect mobility of 17 cm²/V‐sec, threshold voltage of 1.1 V, on/off ratio >10⁹, and subthreshold gate swing of 0.28 V/dec. The AMOLED display with a‐IGZO TFT array is promising for large‐sized applications such as notebook PCs and HDTVs because the a‐IGZO semiconductor can be deposited on large glass substrates (larger than Gen 7) using the conventional sputtering system.     

The k-simultaneous consensus problem

This paper introduces and investigates the k-simultaneous consensus task: each process participates at the same time in k independent consensus instances until it decides in any one of them. It is shown that the k-simultaneous consensus task is equivalent to the k-set agreement task in the wait-free read/write shared memory model, and furthermore k-simultaneous consensus possesses properties that k-set does not. In particular we show that the multivalued version and the binary version of the k-simultaneous consensus task are wait-free equivalent. These equivalences are independent of the number of processes. Interestingly, this provides us with a new characterization of the k-set agreement task that is based on the fundamental binary consensus problem.     

Universal constructions that ensure disjoint-access parallelism and wait-freedom

A universal construction is a general mechanism for obtaining a concurrent implementation of an object from its sequential code. We show that there is no universal construction that is both disjoint-access parallel (guaranteeing the processes operating on different parts of an implemented object do not interfere with one another) and wait-free (guaranteeing progress for each nonfaulty process when accessing an object). In contrast, we present a universal construction which results in disjoint-access parallel, wait-free implementations of any object provided there is a bound on the number of data items accessed by each operation supported by the object.     

Content-Dependent Question Generation Using LOD for History Learning in Open Learning Space

The objective of this research is to use current linked open data (LOD) to generate questions automatically to support history learning. This paper tries to clarify the potential of LOD as a learning resource. By linking LOD to natural language documents, we created an open learning space where learners have access to machine understandable natural language information about many topics. The learning environment supports learners with content-dependent questions. In this paper, we describe the question generation method that creates natural language questions using LOD. The integrated data is combined to a history domain ontology and a history dependent question ontology to generate content-dependent questions. To prove whether the generated questions have a potential to support learning, a human expert conducted an evaluation comparing our automatically generated questions with questions generated manually. The results of the evaluation showed that the generated questions could cover more than 80% of the questions supporting knowledge acquisition generated by humans. In addition, we confirmed the automatically generated questions have a potential to reinforce learners’ deep historical understanding.     

Correlated fluorescence lifetime and spectral measurements in living cells

Studies of proteins' interaction in cells by FRET can take benefit from two important photo-physical properties describing fluorescent proteins: fluorescence emission spectrum and fluorescence lifetime. These properties provide specific and complementary information about the tagged proteins and their environment. However, none of them taken individually can completely quantify the involved fluorophore characteristics due to their multiparametric dependency with molecular environment, experimental conditions, and interpretation complexity. A solution to get a better understanding of the biological process implied at the cellular level is to combine the spectral and temporal fluorescence data acquired simultaneously at every cell region under investigation. We present the SLiM-SPRC160, an original temporal/spectral acquisition system for simultaneous lifetime measurements in 16 spectral channels directly attached to the descanned port of a confocal microscope with two-photon excitation. It features improved light throughput, enabling low-level excitation and minimum invasivity in living cells studies. To guarantee a fairly good level of accuracy and reproducibility in the measurements of fluorescence lifetime and spectra on living cells, we propose a rigorous protocol for running experiments with this new equipment that preserves cell viability. The usefulness of SLiM approach for the precise determination of overlapping fluorophores is illustrated with the study of known solutions of rhodamine. Then, we describe reliable FRET experiments in imaging mode realized in living cells using this protocol. We also demonstrate the benefit of localized fluorescence spectrum-lifetime acquisitions for the dynamic study of fluorescent proteins. proteins.