151 research outputs found

    CONTRIBUTION TO THE STUDY BY X-RAY PHOTOELECTRON SPECTROSCOPY OF THE NATURAL AGING OF THE POLYPROPYLENE

    Get PDF
    In the present work we are concerned in the study, by means of the X-ray Photoelectron Spectroscopy (XPS), of the solar radiation impact (atmospheric environment), on the natural aging of the polypropylene (PP). The study has focused on two periods of aging, 60 and 80 days. Results of the quantitative analysis show an important degradation of the aged material due essentially to the contamination by oxygen, The latter being the main contaminating agent in surface. The solar radiation accelerates the oxidation of the surface of the PP by rupture of the C-H bonds. The decomposition of C1s and O1s peaks has allowed a best comprehension of the chemical reactional mechanisms, in terms of carbon-oxygen bonds (C=O, C-OH and O=C-O) responsible of the photo-oxidation.In the present work we are concerned in the study, by means of the X-ray Photoelectron Spectroscopy (XPS), of the solar radiation impact (atmospheric environment), on the natural aging of the polypropylene (PP). The study has focused on two periods of aging, 60 and 80 days. Results of the quantitative analysis show an important degradation of the aged material due essentially to the contamination by oxygen, The latter being the main contaminating agent in surface. The solar radiation accelerates the oxidation of the surface of the PP by rupture of the C-H bonds. The decomposition of C1s and O1s peaks has allowed a best comprehension of the chemical reactional mechanisms, in terms of carbon-oxygen bonds (C=O, C-OH and O=C-O) responsible of the photo-oxidation

    Gene expression in lungs of mice lacking the 5-hydroxytryptamine transporter gene

    Get PDF
    <p>Abstract</p> <p>Background</p> <p>While modulation of the serotonin transporter (5HTT) has shown to be a risk factor for pulmonary arterial hypertension for almost 40 years, there is a lack of in vivo data about the broad molecular effects of pulmonary inhibition of 5HTT. Previous studies have suggested effects on inflammation, proliferation, and vasoconstriction. The goal of this study was to determine which of these were supported by alterations in gene expression in serotonin transporter knockout mice.</p> <p>Methods</p> <p>Eight week old normoxic mice with a 5-HTT knock-out (5HTT-/-) and their heterozygote(5HTT+/-) or wild-type(5HTT+/+) littermates had right ventricular systolic pressure(RVSP) assessed, lungs collected for RNA, pooled, and used in duplicate in Affymetrix array analysis. Representative genes were confirmed by quantitative RT-PCR and western blot.</p> <p>Results</p> <p>RVSP was normal in all groups. Only 124 genes were reliably changed between 5HTT-/- and 5HTT+/+ mice. More than half of these were either involved in inflammatory response or muscle function and organization; in addition, some matrix, heme oxygenase, developmental, and energy metabolism genes showed altered expression. Quantitative RT-PCR for examples from each major group confirmed changes seen by array, with an intermediate level in 5HTT +/- mice.</p> <p>Conclusion</p> <p>These results for the first time show the in vivo effects of 5HTT knockout in lungs, and show that many of the downstream mechanisms suggested by cell culture and ex vivo experiments are also operational in vivo. This suggests that the effect of 5HTT on pulmonary vascular function arises from its impact on several systems, including vasoreactivity, proliferation, and immune function.</p

    Nebulization of the acidified sodium nitrite formulation attenuates acute hypoxic pulmonary vasoconstriction

    Get PDF
    <p>Abstract</p> <p>Background</p> <p>Generalized hypoxic pulmonary vasoconstriction (HPV) occurring during exposure to hypoxia is a detrimental process resulting in an increase in lung vascular resistance. Nebulization of sodium nitrite has been shown to inhibit HPV. The aim of this project was to investigate and compare the effects of nebulization of nitrite and different formulations of acidified sodium nitrite on acute HPV.</p> <p>Methods</p> <p><it>Ex vivo </it>isolated rabbit lungs perfused with erythrocytes in Krebs-Henseleit buffer (adjusted to 10% hematocrit) and <it>in vivo </it>anesthetized catheterized rabbits were challenged with periods of hypoxic ventilation alternating with periods of normoxic ventilation. After baseline hypoxic challenges, vehicle, sodium nitrite or acidified sodium nitrite was delivered via nebulization. In the <it>ex vivo </it>model, pulmonary arterial pressure and nitric oxide concentrations in exhaled gas were monitored. Nitrite and nitrite/nitrate were measured in samples of perfusion buffer. Pulmonary arterial pressure, systemic arterial pressure, cardiac output and blood gases were monitored in the <it>in vivo </it>model.</p> <p>Results</p> <p>In the <it>ex vivo </it>model, nitrite nebulization attenuated HPV and increased nitric oxide concentrations in exhaled gas and nitrite concentrations in the perfusate. The acidified forms of sodium nitrite induced higher levels of nitric oxide in exhaled gas and had longer vasodilating effects compared to nitrite alone. All nitrite formulations increased concentrations of circulating nitrite to the same degree. In the <it>in vivo </it>model, inhaled nitrite inhibited HPV, while pulmonary arterial pressure, cardiac output and blood gases were not affected. All nitrite formulations had similar potency to inhibit HPV. The tested concentration of appeared tolerable.</p> <p>Conclusion</p> <p>Nitrite alone and in acidified forms effectively and similarly attenuates HPV. However, acidified nitrite formulations induce a more pronounced increase in nitric oxide exhalation.</p

    Impact of interleukin-6 on hypoxia-induced pulmonary hypertension and lung inflammation in mice

    Get PDF
    <p>Abstract</p> <p>Background</p> <p>Inflammation may contribute to the pathogenesis of various forms of pulmonary hypertension (PH). Recent studies in patients with idiopathic PH or PH associated with underlying diseases suggest a role for interleukin-6 (IL-6).</p> <p>Methods</p> <p>To determine whether endogenous IL-6 contributes to mediate hypoxic PH and lung inflammation, we studied IL-6-deficient (IL-6<sup>-/-</sup>) and wild-type (IL-6<sup>+/+</sup>) mice exposed to hypoxia for 2 weeks.</p> <p>Results</p> <p>Right ventricular systolic pressure, right ventricle hypertrophy, and the number and media thickness of muscular pulmonary vessels were decreased in IL-6<sup>-/- </sup>mice compared to wild-type controls after 2 weeks' hypoxia, although the pressure response to acute hypoxia was similar in IL-6<sup>+/+ </sup>and IL-6<sup>-/- </sup>mice. Hypoxia exposure of IL-6<sup>+/+ </sup>mice led to marked increases in IL-6 mRNA and protein levels within the first week, with positive IL-6 immunostaining in the pulmonary vessel walls. Lung IL-6 receptor and gp 130 (the IL-6 signal transducer) mRNA levels increased after 1 and 2 weeks' hypoxia. In vitro studies of cultured human pulmonary-artery smooth-muscle-cells (PA-SMCs) and microvascular endothelial cells revealed prominent synthesis of IL-6 by PA-SMCs, with further stimulation by hypoxia. IL-6 also markedly stimulated PA-SMC migration without affecting proliferation. Hypoxic IL-6<sup>-/- </sup>mice showed less inflammatory cell recruitment in the lungs, compared to hypoxic wild-type mice, as assessed by lung protein levels and immunostaining for the specific macrophage marker F4/80, with no difference in lung expression of adhesion molecules or cytokines.</p> <p>Conclusion</p> <p>These data suggest that IL-6 may be actively involved in hypoxia-induced lung inflammation and pulmonary vascular remodeling in mice.</p

    Lessons learned from cancer may help in the treatment of pulmonary hypertension

    No full text

    Production of TiB2 in an auxiliary iron bath

    No full text
    Lebeau and Figueras introduced the use of liquid metals as media for the synthesis of compounds. The process consists of promoting the reaction of elements by dissolving them in a metallic liquid. One method, known as the auxiliary metal bath process, or the Menstruum process, is used for the production of hard metals. Similarly, mixed carbides of WC, TiC and TaC are produced according to the so-called McKenna process. It is also possible to make silicides, nitrides, carbonitrides and some borides by the auxiliary metal bath process. However, little information is available on the production of TiB2 in auxiliary metal bath, and the present work was undertaken to study its formation in an iron bath. The metallic baths were formed by melting mixtures of ferroboron and ferrotitanium powders. A characterization of the reaction products with respect to the composition of the metallic bath and the temperature of formation is presented.Peer reviewed: YesNRC publication: Ye
    corecore