110 research outputs found

    Brasil: imágenes exportadas y turismo

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    Actas de las Terceras Jornadas Imagen, Cultura y Tecnología celebradas del 28 al 30 de julio de 2004 en la Universidad Carlos III de Madri

    Sediment Contamination and Toxicity in the Guadalquivir River (Southwest, Spain)

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    A segment of the Guadalquivir River was assessed between the Alcalá del Río dam and Seville through an integrative sediment quality assessment. Chemical concentrations of metals and toxicity under laboratory conditions were used as lines of evidence. A battery of bioassays with four organisms (the amphipod Ampelisca brevicornis, the bacteria Vibrio fischeri, the sea urchin Paracentrotus lividus, and the oligochaete Tubifex tubifex) exposed to sediment made it possible to determine the potential risk associated. The sediments from Seville and Alcalá del Río showed higher values of the concentration of most metals than the Algaba station, with Cu (35–37 µg/g), Zn (70–75 µg/g), Ni (23–26 µg/g), and Pb (27–30 µg/g) being the most abundant metals. An increasing toxicity gradient was shown downstream among the bioassays with the amphipod A. brevicornis, the fertilization test using the sea urchin P. lividus, and the freshwater worm growth T. tubifex. Conversely, an increasing toxicity gradient was shown upstream in the embryo-larval P. lividus development. The link between sediment contamination and toxicity makes it possible to obtain a gradient of contaminant concentration comparable with nationally and internationally widely accepted sediment quality guidelines in order to establish the risk associated with this area of study.13 página

    La interferencia retroactiva entre claves entrenadas por separado: evidencia empírica y enfoques teóricos

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    Retroactive interference between cues trained apart was long ago studied in the psychology of memory, within the paired associate tradition. Current theories of learning, however, predict that interference between cues should not occur if they are trained elementally. Here we review the available evidence on retroactive interference between cues trained apart and show that this effect is very similar to other, classical effects, in the area of learning, such as interference between outcomes and competition between cues. We suggest that a stronger connection between these research areas is important, as common mechanisms are quite possibly responsible for all these effects. Finally, we discuss whether associative or the causal inference mechanisms currently studied in the area of learning could provide a satisfactory explanation for these effects.La interferencia retroactiva entre claves entrenadas elementalmente fue en su día un fenómeno muy estudiado en la psicología de la memoria, dentro de la tradición de los pares asociados. Sin embargo, las teorías actuales del aprendizaje predicen que no debería ocurrir interferencia entre claves si estas se entrenan por separado. En este trabajo revisamos la evidencia disponible y mostramos que la interferencia entre claves tiene enormes similitudes con otros efectos clásicos del aprendizaje, especialmente con los efectos de interferencia entre resultados y de competición entre claves. Postulamos, por tanto, que tiene sentido establecer una mayor conexión entre todas estas áreas de investigación y plantear que es muy posible que todos estos efectos sean debidos a mecanismos comunes. Finalmente discutimos si los procesos asociativos o los procesos de inferencia causal que se estudian actualmente en la psicología del aprendizaje podrían dar cuenta de estos efectos

    Mujeres en pie de paz: exclusión y memoria de las mujeres víctimas del conflicto armado desde sus territorios

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    La Constitución de 1991 abrió una oportunidad para que Colombia, luego de diferentes procesos de paz maltrechos, construyera las bases de un contrato social que evitara la exclusión y la desigualdad social, económica y política de una buena parte de la población, sobre todo la campesina. La exclusión y la desigualdad son algunas de las principales causas y orígenes del conflicto colombiano (Alape, 2004; Centro Nacional de Memoria Histórica, 2013), por más de que no exista una única versión sobre cuándo y por qué inició la guerra en Colombia (Comisión Histórica del Conflicto y sus Víctimas [CHCV], 2015). A pesar de que algunos grupos guerrilleros se incorporaron a la vida política institucional y fueron garantes del nuevo pacto social, la nueva Constitución fue una oportunidad perdida. Las desigualdades y la exclusión no cesaron para muchos colombianos y colombianas y el conflicto armado se recrudeció en la última década del siglo XX

    Acetylation of Eugenol on Functionalized Mesoporous Aluminosilicates Synthesized from Amazonian Flint Kaolin

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    The present work was aimed to investigate the catalytic activity of a mesoporous catalyst synthesized from 3-mercaptopropyltrimethoxysilane (MPTS) functionalized Amazonian flint kaolin in the acetylation of eugenol with acetic anhydride. Materials were characterized by thermogravimetry (TGA), N2 adsorption (BET), X-ray dispersive energy spectroscopy (EDX), X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR) and acid-base titration. The results presented proved the efficiency of flint kaolin as an alternative source in the preparation of mesoporous materials, since the material exhibited textural properties (specific surface area of 1071 m2 g−1, pore volume of 1.05 cm3 g−1 and pore diameter of 3.85 nm) and structural properties (d100 = 4.35 nm, a0 = 5.06 nm and Wt = 1.21 nm) within the required and characteristic material standards. The catalyst with the total amount of acidic sites of 4.89 mmol H+ g−1 was efficient in converting 99.9% of eugenol (eugenol to acetic anhydride molar ratio of 1:5, 2% catalyst, temperature and reaction time 80 °C and 40 min reaction). In addition, the reused catalyst could be successfully recycled with 92% conversion activity under identical reaction conditions

    Best practices for expansion of smoke-free and aerosol-free environments in Europe: Protocol for the consultation to experts

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    Smoke-free legislation has been shown to positively impact reducing secondhand smoke (SHS) exposure, especially in countries that have implemented comprehensive legislation rather than partial bans. Also, secondhand aerosols (SHA) that come from the heating of tobacco or liquids, with or without nicotine, in electronic nicotine delivery systems (ENDS) have been proven to increase levels of harmful substances in the air. Therefore, protection against SHS and SHA exposure and expansion of smoke- and aerosol-free environments (SAFE) should be taken into account when creating or trying to expand or enforce clean air policies. This article aims to present the protocol for a consultation with experts on tobacco and nicotine control in order to identify best practices, barriers, and opportunities for the expansion of SAFE in Europe. We identified experts among policymakers, researchers, and tobacco regulators in European countries and invited them to participate in the consultation by completing an online survey designed, programmed, and pilot-tested using Survey Monkey. The responses to the questionnaire contained quantitative and qualitative information that was thematically analyzed. The experts’ consultation allowed us to produce a report on barriers and opportunities for SAFE, a report and a position paper on SAFE best practices, a web-based repository of best practices, and a weight of evidence paper that assembles evidence supporting the expansion of SAFE on indoor and outdoor spaces

    Novel anti-invasive properties of a Fascin1 inhibitor on colorectal cancer cells

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    Tumor invasion and metastasis involve processes in which actin cytoskeleton rearrangement induced by Fascin1 plays a crucial role. Indeed, Fascin1 has been found overexpressed in tumors with worse prognosis. Migrastatin and its analogues target Fascin1 and inhibit its activity. However, there is need for novel and smaller Fascin1 inhibitors. The aim of this study was to assess the effect of compound G2 in colorectal cancer cell lines and compare it to migrastatin in in vitro and in vivo assays. Molecular modeling, actin-bundling, cell viability, inmunofluorescence, migration, and invasion assays were carried out in order to test anti-migratory and anti-invasive properties of compound G2. In addition, the in vivo effect of compound G2 was evaluated in a zebrafish model of invasion. HCT-116 cells exhibited the highest Fascin1 expression from eight tested colorectal cancer cell lines. Compound G2 showed important inhibitory effects on actin bundling, filopodia formation, migration, and invasion in different cell lines. Moreover, compound G2 treatment resulted in significant reduction of invasion of DLD-1 overexpressing Fascin1 and HCT-116 in zebrafish larvae xenografts; this effect being less evident in Fascin1 known-down HCT-116 cells. This study proves, for the first time, the in vitro and in vivo anti-tumoral activity of compound G2 on colorectal cancer cells and guides to design improved compound G2-based Fascin1 inhibitors. Key messages center dot Fascin is crucial for tumor invasion and metastasis and is overexpressed in bad prognostic tumors. center dot Several adverse tumors overexpress Fascin1 and lack targeted therapy. center dot Anti-fascin G2 is for the first time evaluated in colorectal carcinoma and compared with migrastatin. center dot Filopodia formation, migration activity, and invasion in vitro and in vivo assays were performed. center dot G2 blocks actin structures, migration, and invasion of colorectal cancer cells as fascin-dependent.Peer reviewe

    Dominant Distal Myopathy 3 (MPD3) Caused by a Deletion in the HNRNPA1 Gene

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    Background and Objectives To determine the genetic cause of the disease in the previously reported family with adult-onset autosomal dominant distal myopathy (myopathy, distal, 3; MPD3). Methods Continued clinical evaluation including muscle MRI and muscle pathology. A linkage analysis with single nucleotide polymorphism arrays and genome sequencing were used to identify the genetic defect, which was verified by Sanger sequencing. RNA sequencing was used to investigate the transcriptional effects of the identified genetic defect. Results Small hand muscles (intrinsic, thenar, and hypothenar) were first involved with spread to the lower legs and later proximal muscles. Dystrophic changes with rimmed vacuoles and cytoplasmic inclusions were observed in muscle biopsies at advanced stage. A single nucleotide polymorphism array confirmed the previous microsatellite-based linkage to 8p22-q11 and 12q13-q22. Genome sequencing of three affected family members combined with structural variant calling revealed a small heterozygous deletion of 160 base pairs spanning the second last exon 10 of the heterogeneous nuclear ribonucleoprotein A1 (HNRNPA1) gene, which is in the linked region on chromosome 12. Segregation of the mutation with the disease was confirmed by Sanger sequencing. RNA sequencing showed that the mutant allele produces a shorter mutant mRNA transcript compared with the wild-type allele Immunofluorescence studies on muscle biopsies revealed small p62 and larger TDP-43 inclusions. Discussion A small exon 10 deletion in the gene HNRNPA1 was identified as the cause of MPD3 in this family. The new HNRNPA1-related phenotype, upper limb presenting distal myopathy, was thus confirmed, and the family displays the complexities of gene identification.Peer reviewe

    Splicing factor SF3B1 is overexpressed and implicated in the aggressiveness and survival of hepatocellular carcinoma

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    Splicing alterations represent an actionable cancer hallmark. Splicing factor 3B subunit 1 (SF3B1) is a crucial splicing factor that can be targeted pharmacologically (e.g. pladienolide-B). Here, we show that SF3B1 is overexpressed (RNA/protein) in hepatocellular carcinoma (HCC) in two retrospective (n = 154 and n = 172 samples) and in five in silico cohorts (n > 900 samples, including TCGA) and that its expression is associated with tumor aggressiveness, oncogenic splicing variants expression (KLF6-SV1, BCL-XL) and decreased overall survival. In vitro, SF3B1 silencing reduced cell viability, proliferation and migration and its pharmacological blockade with pladienolide-B inhibited proliferation, migration, and formation of tumorspheres and colonies in liver cancer cell lines (HepG2, Hep3B, SNU-387), whereas its effects on normal-like hepatocyte-derived THLE-2 proliferation were negligible. Pladienolide-B also reduced the in vivo growth and the expression of tumor-markers in Hep3B-induced xenograft tumors. Moreover, SF3B1 silencing and/or blockade markedly modulated the activation of key signaling pathways (PDK1, GSK3b, ERK, JNK, AMPK) and the expression of cancer-associated genes (CDK4, CD24) and oncogenic SVs (KLF6-SV1). Therefore, the genetic and/or pharmacological inhibition of SF3B1 may represent a promising novel therapeutic strategy worth to be explored through randomized controlled trials.Las alteraciones en el splicing son un rasgo distintivo del cáncer. La subunidad 1 del factor de splicing 3B (SF3B1) es un factor de splicing crucial que puede ser objeto de tratamiento farmacológico (por ejemplo, pladienolide-B). En este estudio demostramos que SF3B1 está sobreexpresado (ARN/proteína) en el carcinoma hepatocelular (CHC) en dos cohortes retrospectivas (n = 154 y n = 172 muestras) y en cinco cohortes in silico (n > 900 muestras, incluyendo TCGA) y que su expresión está asociada con la agresividad tumoral, la expresión de variantes de splicing oncogénicas (KLF6-SV1, BCL-XL) y la disminución de la supervivencia global. In vitro, el silenciamiento de SF3B1 redujo la viabilidad, proliferación y migración celular, y su bloqueo farmacológico con pladienolide-B inhibió la proliferación, migración y formación de esferas tumorales y colonias en líneas celulares de cáncer de hígado (HepG2, Hep3B, SNU-387), mientras que sus efectos sobre la proliferación de THLE-2 derivadas de hepatocitos de tipo normal fueron insignificantes. Pladienolide-B también redujo el crecimiento in vivo y la expresión de marcadores tumorales en tumores xenoinjertados inducidos por Hep3B. Además, el silenciamiento y/o bloqueo de SF3B1 moduló notablemente la activación de vías de señalización clave (PDK1, GSK3b, ERK, JNK, AMPK) y la expresión de genes asociados al cáncer (CDK4, CD24) y de SV oncogénicos (KLF6-SV1)

    Effects of α-tocopherol and ternatin antioxidants on morphology and activation of goat preantral follicles in vitro cultured

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    Os efeitos do α-tocoferol e da ternatina sobre morfologia, ativação e crescimento de folículos pré-antrais caprinos cultivados in vitro, por um ou cinco dias, foram avaliados. Os fragmentos ovarianos foram imediatamente fixados (controle não-cultivado) ou cultivados in vitro, por um ou cinco dias, em Meio Essencial Mínimo (MEM) com ou sem suplementação com α-tocoferol ou ternatina nas concentrações de 5, 10 ou 15M, formando os tratamentos MEM, TOC5, TOC10, TOC 15, TER5, TER10, TER15. O percentual de folículos pré-antrais normais no controle não-cultivado foi de 73,2%, depois de cinco dias de cultivo, houve redução desse percentual em todos os tratamentos, quando comparados com o controle não-cultivado (P<0,05). O cultivo por cinco dias aumentou a ativação folicular em todos os tratamentos (P<0,05). A análise ultra-estrutural não mostrou folículos pré-antrais íntegros após cinco dias de cultivo em meio contendo antioxidantes. Concluiu-se que o α -tocoferol e a ternatina podem promover a ativação folicular, no entanto a adição desses antioxidantes nas concentrações testadas reduziu a viabilidade folicular após o cultivo in vitro. ______________________________________________________________________________________________________________ ABSTRACTThe effects of α-tocopherol and ternatin on the morphology, activation, and growth of goat preantral follicles in vitro cultured, for one or five days, were evaluated. Ovarian fragments were immediately fixed (non-cultured control) or in vitro cultured for one or five days in Minimum Essential Medium (MEM) with or without α-tocopherol or ternatin supplementation, both at concentrations of 5, 10, or 15M, corresponding to the following treatments: MEM, TOC5, TOC10, TOC 15, TER5, TER10, and TER15. The percentages of morphologically normal preantral follicles in non-cultured ovarian tissue (control) was 73.2% and after five days of culture, there was a decrease on these percentages in all treatments (P<0.05) when compared with non-cultured control. Culture of ovarian cortex for five days increased the percentages of follicular activation in all treatments (P<0.05). Ultrastructural analysis did not confirm the integrity of caprine preantral follicles cultured for five days in medium containing antioxidants. This study demonstrated that α-tocopherol and ternatin can promote follicular activation; however, addition of these antioxidants in the tested concentrations reduced the follicular viability after in vitro culture
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