33 research outputs found

    Spectrophotometric Observations of Blue Compact Dwarf Galaxies: Mrk 370

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    We present results from a detailed spectrophotometric analysis of the blue compact dwarf galaxy (BCD) Mrk 370, based on deep UBVRI broad-band and Halpha narrow-band observations, and long-slit and two-dimensional spectroscopy of its brightest knots. The spectroscopic data are used to derive the internal extinction, and to compute metallicities, electronic density and temperature in the knots. By subtracting the contribution of the underlying older stellar population, modeled by an exponential function, removing the contribution from emission lines, and correcting for extinction, we can measure the true colors of the young star-forming knots. We show that the colors obtained this way differ significantly from those derived without the above corrections, and lead to different estimates of the ages and star-forming history of the knots. Using predictions of evolutionary synthesis models, we estimate the ages of both the starburst regions and the underlying stellar component. We found that we can reproduce the colors of all the knots with an instantaneous burst of star formation and the Salpeter initial mass function with an upper mass limit of 100 solar masses. The resulting ages range between 3 and 6 Myrs. The colors of the low surface brightness component are consistent with ages larger than 5 Gyr. The kinematic results suggest ordered motion around the major axis of the galaxy.Comment: 26 pages with 14 figures; accepted for publication in Ap

    SHARDS: A global view of the star formation activity at z~0.84 and z~1.23

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    In this paper, we present a comprehensive analysis of star-forming galaxies (SFGs) at intermediate redshifts (z~1). We combine the ultra-deep optical spectro-photometric data from the Survey for High-z Absorption Red and Dead Sources (SHARDS) with deep UV-to-FIR observations in the GOODS-N field. Exploiting two of the 25 SHARDS medium-band filters, F687W17 and F823W17, we select [OII] emission line galaxies at z~0.84 and z~1.23 and characterize their physical properties. Their rest-frame equivalent widths (EWrf_{\mathrm{rf}}([OII])), line fluxes, luminosities, star formation rates (SFRs) and dust attenuation properties are investigated. The evolution of the EWrf_{\mathrm{rf}}([OII]) closely follows the SFR density evolution of the universe, with a trend of EWrf_{\mathrm{rf}}([OII])\propto(1+z)3^3 up to redshift z~1, followed by a possible flattening. The SF properties of the galaxies selected on the basis of their [OII] emission are compared with complementary samples of SFGs selected by their MIR and FIR emission, and also with a general mass-selected sample of galaxies at the same redshifts. We demonstrate observationally that the UVJ diagram (or, similarly, a cut in the specific SFR) is only partially able to distinguish the quiescent galaxies from the SFGs. The SFR-M_* relation is investigated for the different samples, yelding a logarithmic slope ~1, in good agreement with previous results. The dust attenuations derived from different SFR indicators (UV(1600), UV(2800), [OII], IR) are compared and show clear trends with respect to both the stellar mass and total SFR, with more massive and highly star-forming galaxies being affected by stronger dust attenuation.Comment: Replaced to match the accepted version (24 pages, 1 table, 17 figures). Published in ApJ, 812, 155 (2015): http://stacks.iop.org/0004-637X/812/15

    Design and rationale of a multicentre, randomised, double-blind, placebo-controlled clinical trial to evaluate the effect of vitamin D on ventricular remodelling in patients with anterior myocardial infarction: the VITamin D in Acute Myocardial Infarction (VITDAMI) trial

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    Introduction:Decreased plasma vitamin D (VD) levels are linked to cardiovascular damage. However, clinical trials have not demonstrated a benefit of VD supplements on left ventricular (LV) remodelling. Anterior ST-elevation acute myocardial infarction (STEMI) is the best human model to study the effect of treatments on LV remodelling. We present a proof-of-concept study that aims to investigate whether VD improves LV remodelling in patients with anterior STEMI. Methods and analysis:The VITamin D in Acute Myocardial Infarction (VITDAMI) trial is a multicentre, randomised, double-blind, placebo-controlled trial. 144 patients with anterior STEMI will be assigned to receive calcifediol 0.266 mg capsules (Hidroferol SGC)/15 days or placebo on a 2:1 basis during 12 months. Primary objective:to evaluate the effect of calcifediol on LV remodelling defined as an increase in LV end-diastolic volume >= 10\% (MRI). Secondary objectives:change in LV end-diastolic and end-systolic volumes, ejection fraction, LV mass, diastolic function, sphericity index and size of fibrotic area; endothelial function; plasma levels of aminoterminal fragment of B-type natriuretic peptide, galectin-3 and monocyte chemoattractant protein-1; levels of calcidiol (VD metabolite) and other components of mineral metabolism (fibroblast growth factor-23 (FGF-23), the soluble form of its receptor klotho, parathormone and phosphate). Differences in the effect of VD will be investigated according to the plasma levels of FGF-23 and klotho. Treatment safety and tolerability will be assessed. This is the first study to evaluate the effect of VD on cardiac remodelling in patients with STEMI. Ethics and dissemination: This trial has been approved by the corresponding Institutional Review Board (IRB) and National Competent Authority (Agencia Espanola de Medicamentos y Productos Sanitarios (AEMPS)). It will be conducted in accordance with good clinical practice (International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use-Good Clinical Practice (ICH-GCP)) requirements, ethical principles of the Declaration of Helsinki and national laws. The results will be submitted to indexed medical journals and national and international meetings.The VITDAMI trial is an investigator initiated study, sponsored by the Instituto de Investigacion Sanitaria Fundacion Jimenez Diaz (IIS-FJD). Funding has been obtained from Fondo de Investigaciones Sanitarias (PI14/01567; http://www.isciii.es/) and Spanish Society of Cardiology (http://secardiologia.es/). In addition, the study medication has been provided freely by the pharmaceutical Company FAES FARMA S.A. (Leioa, Vizcaya, Spain; http://faesfarma.com/). This company was the only funder who collaborated in study design (IG-H).S

    Deep Near Infrared Mapping of Young and Old Stars in Blue Compact Dwarf Galaxies

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    We analyze J, H and Ks near-infrared data for 9 Blue Compact Dwarf (BCD) galaxies, selected from a larger sample that we have already studied in the optical. We present contour maps, surface brightness and color profiles, as well as color maps of the sample galaxies. The morphology of the BCDs in the NIR has been found to be basically the same as in the optical. The inner regions of these systems are dominated by the starburst component. At low surface brightness levels the emission is due to the underlying host galaxy; the latter is characterized by red, radially constant colors and isophotes well fit by ellipses. We derive accurate optical near--infrared host galaxy colors for eight of the sample galaxies; these colors are typical of an evolved stellar population. Interestingly, optical near--infrared color maps reveal the presence of a complex, large-scale absorption pattern in three of the sample galaxies. We study the applicability of the Sersic law to describe the surface brightness profiles of the underlying host galaxy, and find that, because of the limited surface brightness interval over which the fit can be made, the derived Sersic parameters are very sensitive to the selected radial interval and to errors in the sky subtraction. Fitting an exponential model gives generally more stable results, and can provide a useful tool to quantify the structural properties of the host galaxy and compare them with those of other dwarf classes as well as with those of star-forming dwarfs at higher redshifts.Comment: 49 pages, 9 figures, 10 tables, accepted for publication in the Astrophysical Journa

    Valoracion por ecocardiografia doppler color de la insuficiencia tricuspide croncia en pacientes con valvulopatia izquierda Estudio comparativo con la angiografia en el laboratorio de hemodinamica

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    Centro de Informacion y Documentacion Cientifica (CINDOC). C/Joaquin Costa, 22. 28002 Madrid. SPAIN / CINDOC - Centro de Informaciòn y Documentaciòn CientìficaSIGLEESSpai

    Cinetoquimica de la oxidacion permanganica de aminoacidos en medio basico: glicina, alanina y fenilalanina

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    Centro de Informacion y Documentacion Cientifica (CINDOC). C/Joaquin Costa, 22. 28002 Madrid. SPAIN / CINDOC - Centro de Informaciòn y Documentaciòn CientìficaSIGLEESSpai

    Drug-loaded PCL electrospun nanofibers as anti-pancreatic cancer drug delivery systems

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    Cancer is one of the main causes of death worldwide, being pancreatic cancer the second deadliest cancer in Western countries. Surgery, chemotherapy and radiotherapy form the basis of pancreatic cancer's current treatment. However, these techniques have several disadvantages, such as surgery complications, chemotherapy systemic side effects and cancer recurrence. Drug delivery systems can reduce side effects, increasing the effectivity of the treatment by a controlled release at the targeted tumor cells. In this context, coaxial electrospun fibers can increase the control on the release profile of the drug. The aim of this study was to encapsulate and release different anticancer drugs (5-Fluorouracil and Methotrexate) from a polymeric fiber mat. Different flows and ratios were used to test their effect on fiber morphology, FTIR spectrum, drug encapsulation and release. Good integration of the anticancer drugs was observed and the use of a desiccator for 24 h showed to be a key step to remove solvent remanence. Moreover, the results of this study demonstrated that the polymeric solution could be used to encapsulate and release different drugs to treat cancers. This makes coaxial electrospinning a promising alternative to deliver complex chemotherapies that involve more than one drug, such as FOLFIRINOX, used in pancreatic cancer treatment

    Halothane induces oxidative stress and NF-kappa B activation in rat liver: Protective effect of propofol

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    We investigated the effects of propofol on markers of oxidative stress, nuclear factor kappa B (NF-kappa B) activation and inducible nitric oxide synthase (NOS) expression in liver of rats treated with halothane under hypoxic conditions. Male Wistar rats received halothane 1% oxygen 14%, oxygen 14%/propofol 60 mg kg(-1) i.p., or halothane 1% oxygen 14%/propofol 60 mg kg(-1) i.p. Morphological examination showed complete loss of architecture with massive necrosis of parenchyma in the halothane group, while only minor histological abnormalities were observed in rats receiving halothane plus propofol. the cytosolic concentration of TBARS and the hydroperoxide-initiated chemiluminescence increased significantly in the liver of animals from the halothane group (+62% and +40% versus controls, respectively), and this increase was abolished by propofol administration. Halothane induced a marked activation of NF-kappa B (+180%), and resulted in a significant decrease of the nonphosphorylated form of the inhibitor I kappa B alpha (-53%), while phosphorylated I kappa B alpha protein level was markedly increased (+ 146%). Propofol administration lowered these effects to +30% (NF-kappa B), -26% (nonphosphorylated I kappa B alpha), and +56% (phosphorylated I kappa B alpha). the increase of WOS protein level (+59%) induced by halothane was significantly reduced to +22% by additional administration of propofol. Results obtained show that administration of propofol inhibits oxidative stress, NF-kappa B nuclear traslocation and Nos overexpression in liver of rats receiving halothane. Propofol treatment, by inhibiting the NF-kappa B signal transduction pathway, might block the production of noxious mediators involved in the development of halothane-induced injury. (c) 2006 Elsevier Ireland Ltd. All rights reserved.Univ Leon, Dept Physiol, E-24071 Leon, SpainIrmandade Santa Casa Misericordia, Porto Alegre, RS, BrazilUniv Luterana Brasil, Porto Alegre, RS, BrazilUniversidade Federal de São Paulo, Dept Anesthesiol & Intens Care Med, São Paulo, BrazilUniversidade Federal de São Paulo, Dept Anesthesiol & Intens Care Med, São Paulo, BrazilWeb of Scienc
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