4,647 research outputs found

    Involvement of leukotriene pathway in the pathogenesis of ischemia-reperfusion injury and septic and non-septic shock.

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    The 5-lipoxygenase (5-LO) pathway is responsible for the production of leukotrienes (LTs), inflammatory lipid mediators which play a role in innate immunity. More recently, a pivotal role of LTs in ischemia-reperfusion and shock injury has been suggested. In fact, these pathological conditions are characterized by a severe neutrophil infiltration that gives rise to tissue injury and 5-LO metabolites control neutrophil recruitment in injured tissue by the modulation of adhesion molecule expression. The aim of this review is to analyze the results reported in the literature on the role of 5-LO pathway, with particular regard to LTs, in these pathological conditions. A better understanding of the mechanisms underlying the role of the 5-LO enzyme and/or its metabolites in the regulation of neutrophil trafficking, might open new perspectives in the therapy of organ dysfunction and/or injury associated with shock and ischemia-reperfusion injury

    Design, implementation and validation of AI-inspired information systems

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    While there is an emerging and always-growing interest for novel paradigms appeared recently (e.g., social networks, Cloud computing, NoSQL databases, Big Data, and so forth), Artificial Intelligence (AI) always plays a critical role in next-generation Information Systems. Indeed, as technology and paradigms pervade our life, there is a challenging need for smarter and more sophisticated Information Systems, for instance using innovative methodologies like crowdsourcing. As a consequence, it is natural to foresee the advancement of a novel class of Information Systems, which we call as AI-Inspired Information Systems. Basically, these are Information Systems which incorporate in their critical layers (i.e., design, implementation, validation) AI methodologies, yet extending their roots to classical foundations, with, indeed, exciting innovations

    Few Graphene layer/Carbon-Nanotube composite Grown at CMOS-compatible Temperature

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    We investigate the growth of the recently demonstrated composite material composed of vertically aligned carbon nanotubes capped by few graphene layers. We show that the carbon nanotubes grow epitaxially under the few graphene layers. By using a catalyst and gaseous carbon precursor different from those used originally we establish that such unconventional growth mode is not specific to a precise choice of catalyst-precursor couple. Furthermore, the composite can be grown using catalyst and temperatures compatible with CMOS processing (T < 450\degree C).Comment: 4 pages, 4 figure

    Inhibition of nitric oxide biosynthesis by anthocyanin fraction of blackberry extract.

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    Anthocyanins are natural colorant belonging to the flavonoid family, widely distributed among flowers, fruits, and vegetables. Some flavonoids have been found to possess anticarcinogenic, cytotoxic, cytostatic, antioxidant, and anti-inflammatory properties. Since increased nitric oxide (NO) plays a role in inflammation, we have investigated whether the pharmacological activity of the anthocyanin fraction of a blackberry extract (cyanidin-3-O-glucoside representing about 88% of the total anthocyanin content) was due to the suppression of NO synthesis. The markedly increased production of nitrites by stimulation of J774 cells with lipopolysaccharide (LPS) for 24 h was concentration-dependently inhibited by the anthocyanin fraction (11, 22, 45, and 90 μg/ml) of the extract. Moreover, this inhibition was dependent on a dual mechanism, since the extract attenuated iNOS protein expression and decreased the iNOS activity in lungs from LPS-stimulated rats. Inhibition of iNOS protein expression appeared to be at the transcriptional level, since the extract and similarly cyanidin-3-O-glucoside (10, 20, 40, and 80 μg/ml, amounts corresponding to the concentrations present in the extract) decreased LPS-induced NF-κB activation, through inhibition of IκBα degradation, and reduced ERK-1/2 phosphorylation in a concentration-dependent manner. In conclusion, our study demonstrates that at least some part of the anti-inflammatory activity of blackberry extract is due to the suppression of NO production by cyanidin-3-O-glucoside, which is the main anthocyanin present in the extract. The mechanism of this inhibition seems to be due to an action on the expression/activity of the enzyme. In particular, the protein expression was inhibited through the attenuation of NF-κB and/or MAPK activatio

    Pietro Paoli, Italian Algebraist

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    Pietro Paoli was a leading Italian mathematician in the late 18th century. His signed letter pertaining to the death of astronomer Giuseppe Antonio Slop is translated from Italian to flowing (American) English

    Robustness to Non-Independence and Power of the I Test for Trend in Construct Validity

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    The Multitrait-Multimethod Matrix is used to evaluate construct validity; Sawilowsky (2002) created the I test to analyze the matrix. This article examined the robustness and power of the Sawilowsky I test. Ad hoc critical values were determined to improve the statistical power of the technique for analyzing the Multitrait-Multimethod Matrix

    Frequent subgraph mining from streams of linked graph structured data

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    Nowadays, high volumes of high-value data (e.g., semantic web data) can be generated and published at a high velocity. A collection of these data can be viewed as a big, interlinked, dynamic graph structure of linked resources. Embedded in them are implicit, previously unknown, and potentially useful knowledge. Hence, ecient knowledge discovery algorithms for mining frequent subgraphs from these dynamic, streaming graph structured data are in demand. Some existing algorithms require very large memory space to discover frequent subgraphs; some others discover collections of frequently co-occurring edges (which may be disjoint). In contrast, we propose|in this paper|algorithms that use limited memory space for discovering collections of frequently co-occurring connected edges. Evaluation results show the effectiveness of our algorithms in frequent subgraph mining from streams of linked graph structured data

    Myrtucommulone from Myrtus communis exhibits potent anti-inflammatory effectiveness in vivo.

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    Myrtucommulone a nonprenylated acylphloroglucinol contained in the leaves of myrtle (Myrtus communis), has been reported to suppress the biosynthesis of eicosanoids by inhibition of 5-lipoxygenase and cyclooxygenase-1 in vitro and to inhibit the release of elastase and the formation of reactive oxygen species in activated polymorphonuclear leukocytes. Here, in view of the ability of MC to suppress typical proinflammatory cellular responses in vitro, we have investigated the effects of MC in in vivo models of inflammation. MC was administered to mice intraperitoneally, and paw edema and pleurisy were induced by the subplantar and intrapleural injection of carrageenan, respectively. MC (0.5, 1.5, and 4.5 mg/kg i.p.) reduced the development of mouse carrageenan-induced paw edema in a dose-dependent manner. Moreover, MC (4.5 mg/kg i.p. 30 min before and after carrageenan) exerted anti-inflammatory effects in the pleurisy model. In particular, 4 h after carrageenan injection in the pleurisy model, MC reduced: 1) the exudate volume and leukocyte numbers; 2) lung injury (histological analysis) and neutrophil infiltration (myeloperoxidase activity); 3) the lung intercellular adhesion molecule-1 and P-selectin immunohistochemical localization; 4) the cytokine levels (tumor necrosis factor-α and interleukin-1 β in the pleural exudate and their immunohistochemical localization in the lung; 5) the leukotriene B 4, but not prostaglandin E2, levels in the pleural exudates; and 6) lung peroxidation (thiobarbituric acid-reactant substance) and nitrotyrosine and poly (ADP-ribose) immunostaining. In conclusion, our results demonstrate that MC exerts potent anti-inflammatory effects in vivo and offer a novel therapeutic approach for the management of acute inflammation. Copyright © 2009 by The American Society for Pharmacology and Experimental Therapeutics
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