996 resultados para Plinio Cecilio Segundo, Cayo, 62-114 d.C..
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Estudiar e investigar sobre el proceso de aprendizaje. Determinar el grado de entendimiento de los alumnos de ciertos conceptos matemáticos. A/ Prueba de lógica: pasada la prueba a 128 estudiantes de COU. B/ Prueba de enunciados: pasada a alumnos de Básica de quinto, sexto, séptimo y octavo, alumnos de BUP y de Formación Profesional. C/ Prueba de funciones: alumnos de séptimo y octavo de EGB, primero y segundo de BUP y primero y segundo de Formación Profesional. D/ Prueba de GeometrÃa. E/ Prueba de probabilidad: alumnos de séptimo y octavo de EGB, y alumnos de primero, segundo y tercero de BUP y COU. En la primera parte se estudian e investigan los conocimientos necesarios para llevar a cabo la investigación y que son: teorÃas del aprendizaje, estadÃstica y su aplicación a problemas de aprendizaje, y utilización del ordenador. En la segunda parte se confeccionan las siguientes pruebas: prueba de implicación lógica, prueba de enunciados, prueba de funciones, prueba de GeometrÃa y prueba de probabilidad. Finalmente, en la tercera parte se analizan los resultados de dichas pruebas. A/ EstadÃstica descriptiva univariante: media, desviación tipica, coeficiente de variación. B/ Covarianza y correlación. C/ Análisis de varianza de un factor. D/ Análisis multivariante: análisis de componentes principales, análisis factorial, problemas de clasificación y asignación, análisis discriminante. Programas de ordenador. Se han obtenido los items más discriminantes para confeccionar una nueva prueba sobre implicación lógica. Se ha comprobado que la variable sexo no incide significativamente en la prueba, aunque sà la variable centro. En la prueba de enunciado se ha evaluado como incide la edad. Para resultados pormenorizados consultar el capÃtulo V.
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Estudiar la droga en los alumnos de BUP en la capital de Salamanca, por ser esta etapa en la que tienen lugar los primeros contactos con ella. En este momento la persona comienza a precisar con exactitud de adulto tanto su entorno como asà mismo. Se tienen que asentar unos conocimiento precisos y objetivos sobre la realidad de la droga por parte de educadores y padres. Demanda del pedagogo especializado. 381 individuos entre 7.807 alumnos, con margen de confianza del 95,5 por ciento y un error del 5 por ciento en el curso 79-80. 6 colegios privados y 3 institutos. Cursos: primero, segundo y tercero de BUP atendiendo a la distinción de sexos y enseñanza estatal o privada. Variables del estudio : a) Alumnos que sà han tomado droga y alumnos que no, b) Cursos: primero, segundo y tercero de BUP, c) Atendiendo a la distinción de sexos, d) Atendiendo a la distinción: enseñanza estatal o enseñanza privada. Encuestas voluntarias, anónimas y aceptadas por la totalidad de alumnos. Cuestionarios para todos los alumnos. Cálculo de porcentajes. No se puede hablar de drogodependientes. Están en un periodo de iniciación e invitación con alta influencia del grupo. Han tomado drogas el 24,6 por ciento del total. Entre segundo y tercero de BUP la mitad a probado alguna sustancia. La más consumida es el canabis. Los varones toman más que las mujeres. La enseñanza estatal alcanza porcentajes más altos que la privada, a excepción de anfetaminas y alucinógenos. La consiguen por invitación de amigos. En la mujer se da mayor número en la compra de la droga. Evalúan de forma negativa a la sociedad y son inconformistas. Viven con sus padres y valoran a la familia positivamente. Considerando a los padres permisivos. Alta influencia del grupo de compañeros a la hora de tomar drogas. Les preocupa la soledad. CrÃtica más dura al colegio y a la educación. Sensibilización alta frente a problemas externos. El adolescente siente curiosidad por lo prohibido, que confirma la poca o ninguna efectividad de todo el programa preventivo, basado en lo negativo. Hay que fomentar un plan centrado en lograr un aprendizaje significativo orientado en formar una persona crÃtica y autónoma frente al entorno, a partir de un aprendizaje por descubrimiento.
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TÃtulo anterior: BoletÃn de la Comisión Española de la UNESCO
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We previously identified the function of the hepatitis C virus (HCV) p7 protein as an ion channel in artificial lipid bilayers and demonstrated that this in vitro activity is inhibited by amantadine. Here we show that the ion channel activity of HCV p7 expressed in mammalian cells can substitute for that of influenza virus M2 in a cell-based assay. This was also the case for the p7 from the related virus, bovine viral diarrhoea virus (BVDV). Moreover, amantadine was shown to abrogate HCV p7 function in this assay at a concentration that specifically inhibits M2. Mutation of a conserved basic loop located between the two predicted trans-membrane alpha helices rendered HCV p7 non-functional as an ion channel. The intracellular localization of p7 was unaffected by this mutation and was found to overlap significantly with membranes associated with mitochondria. Demonstration of p7 ion channel activity in cellular membranes and its inhibition by amantadine affirm the protein as a target for future anti-viral chemotherapy.
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Hepatitis C virus (HCV) infection is associated with dysregulation of both lipid and glucose metabolism. As well as contributing to viral replication, these perturbations influence the pathogenesis associated with the virus, including steatosis, insulin resistance, and type 2 diabetes. AMP-activated protein kinase (AMPK) plays a key role in regulation of both lipid and glucose metabolism. We show here that, in cells either infected with HCV or harboring an HCV subgenomic replicon, phosphorylation of AMPK at threonine 172 and concomitant AMPK activity are dramatically reduced. We demonstrate that this effect is mediated by activation of the serine/threonine kinase, protein kinase B, which inhibits AMPK by phosphorylating serine 485. The physiological significance of this inhibition is demonstrated by the observation that pharmacological restoration of AMPK activity not only abrogates the lipid accumulation observed in virus-infected and subgenomic replicon-harboring cells but also efficiently inhibits viral replication. These data demonstrate that inhibition of AMPK is required for HCV replication and that the restoration of AMPK activity may present a target for much needed anti-HCV therapies.
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An estimated 3% of the global population are infected with hepatitis C virus (HCV), and the majority of these individuals will develop chronic liver disease. As with other chronic viruses, establishment of persistent infection requires that HCV-infected cells must be refractory to a range of pro-apoptotic stimuli. In response to oxidative stress, amplification of an outward K(+) current mediated by the Kv2.1 channel, precedes the onset of apoptosis. We show here that in human hepatoma cells either infected with HCV or harboring an HCV subgenomic replicon, oxidative stress failed to initiate apoptosis via Kv2.1. The HCV NS5A protein mediated this effect by inhibiting oxidative stress-induced p38 MAPK phosphorylation of Kv2.1. The inhibition of a host cell K(+) channel by a viral protein is a hitherto undescribed viral anti-apoptotic mechanism and represents a potential target for antiviral therapy.
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The permeability parameter (C) for the movement of cephalosporin C across the outer membrane of Pseudomonas aeruginosa was measured using the widely accepted method of Zimmermann & Rosselet. In one experiment, the value of C varied continuously from 4·2 to 10·8 cm3 min-1 (mg dry wt cells)-1 over a range of concentrations of the test substrate, cephalosporin C, from 50 to 5 μm. Dependence of C on the concentration of test substrate was still observed when the effect of a possible electric potential difference across the outer membrane was corrected for. In quantitative studies of β-lactam permeation the dependence of C on the concentration of β-lactam should be taken into account.
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The state-resolved reactivity of CH4 in its totally symmetric C-H stretch vibration (�1) has been measured on a Ni(100) surface. Methane molecules were accelerated to kinetic energies of 49 and 63:5 kJ=mol in a molecular beam and vibrationally excited to �1 by stimulated Raman pumping before surface impact at normal incidence. The reactivity of the symmetric-stretch excited CH4 is about an order of magnitude higher than that of methane excited to the antisymmetric stretch (�3) reported by Juurlink et al. [Phys. Rev. Lett. 83, 868 (1999)] and is similar to that we have previously observed for the excitation of the first overtone (2�3). The difference between the state-resolved reactivity for �1 and �3 is consistent with predictions of a vibrationally adiabatic model of the methane reaction dynamics and indicates that statistical models cannot correctly describe the chemisorption of CH4 on nickel.
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Background: ABCA1 plays an important role in HDL metabolism. Single nucleotide polymorphisms (SNPs) in ABCA1 gene were associated with variation in plasina HDL-c. Methods: The effect of the ABCA1 SNPs C-14T, R219K and of a novel variant C-105T on serum lipids was investigated in 367 unrelated Brazilian individuals (224 hypercholesterolemic and 143 normolipidemic). The relation between ABCA1 SNPs and the lipid-lowering response to atorvastatin (10 mg/day/4 weeks) was also evaluated in 141 hypercholesterolemic (HC) individuals. The polymorphisms were detected by PCRR_FLP and confirmed by DNA sequencing. Results: Linkage disequilibrium was found between the SNPs C-105T and C-14T in the HC group. HC individuals carrying - 105CT/TT genotypes had higher serum HDL-c and lower triglyceride and VLDL-c concentrations as well as lower TG/HDL-c ratio compared to the -105CC carriers (p<0.05). The R219K SNP was associated with reduced serum triglyceride, VLDL-c and TG/HDL-c ratio in the HC group (p<0.05), and with an increased serum apoAI in NL individuals. The effects of ABCA1 SNPs on basal serum lipids of HC individuals were not modified by atorvastatin treatment. Conclusions: The ABCA1 SNPs R219K and C-105T were associated with a less atherogenic lipid profile but not with the lowering-cholesterol response to atorvastatin in a Brazilian population. (C) 2007 Elsevier B.V. All rights reserved.
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Marine organisms have been shown to be potential sources of bioactive compounds with pharmaceutical applications. Previous chemical investigation of the nudibranch Tambja eliora led to the isolation of the alkaloid tambjamine D. Tambjamines have been isolated from marine sources and belong to the family of 4-methoxypyrrolic-derived natural products, which display promising immunosuppressive and cytotoxic properties. Their ability to intercalate DNA and their pro-oxidant activity may be related to some of the biological effects of the 4-methoxypyrrolic alkaloids. The aim of the present investigation was to determine the cytotoxic, pro-oxidant and genotoxic properties of tambjamine D in V79 Chinese hamster lung fibroblast cells. Tambjamine D displayed a potent cytotoxic effect in V79 cells (IC50 1.2 mu g/mL) evaluated by the MTT assay. Based on the MTT result, V79 cells were treated with different concentrations of tambjamine D (0.6. 1.2. 2.4 and 4.8 mu g/mL). After 24 h, tambjamine D reduced the number of viable cells in a concentration-dependent way at all concentrations tested. assessed by the trypan blue dye exclusion test. The hemolytic assay showed that the cytotoxic activity of tambjamine D was not related to membrane disruption (EC50 > 100 mu g/mL). Tambjamine D increased the number of apoptotic cells in a concentration-dependent manner at all concentrations tested according to acridine orange/ethidium bromide staining, showing that the alkaloid cytotoxic effect was related to the induction of apoptosis. MTT reduction was stimulated by tambjamine D, which may indicate the generation of reactive oxygen species. Accordingly, treatment of cells with tambjamine D increased nitrite/nitrate at all concentrations and TBARS production starting at the concentration corresponding to the IC50. Tambjamine D, also, induced DNA strand breaks and increased the micronucleus cell frequency as evaluated by comet and micronucleus tests, respectively, at all concentrations evaluated. showing a genotoxic risk induced by tambjamine D. (C) 2008 Elsevier Ireland Ltd. All rights reserved.
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A carbon-supported binary Pt(3)Sn catalyst has been prepared using a modified polymeric precursor method under controlled synthesis conditions This material was characterized using X-ray diffraction (XRD). and the results indicate that 23% (of a possible 25%) of Sn is alloyed with Pt, forming a dominant Pt(3)Sn phase. Transmission election microscopy (TEM) shows good dispersion of the electrocatalyst and small particle sizes (3 6 nm +/- 1 nm) The polarization curves for a direct ethanol fuel cell using Pt(3)Sn/C as the anode demonstrated Improved performance compared to that of a PtSn/C E-TEK. especially in the intrinsic resistance-controlled and mass transfer regions. This behavior is probably associated with the Pt(3)Sn phase. The maximum power density for the Pt(3)Sn/C electrocatalyst (58 mW cm(-2)) is nearly twice that of a PtSn/C E-TEK electrocatalyst (33 mW cm(-2)) This behavior is attributed to the presence of a mixed Pt(9)Sn and Pt(3)Sn alloy phase in the commercial catalysts (C) 2009 Elsevier B V All rights reserved
Ethanol oxidation reaction on PtCeO(2)/C electrocatalysts prepared by the polymeric precursor method
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This paper presents a study of the electrocatalysis of ethanol oxidation reactions in an acidic medium on Pt-CeO(2)/C (20 wt.% of Pt-CeO(2) on carbon XC-72R), prepared in different mass ratios by the polymeric precursor method. The mass ratios between Pt and CeO(2) (3:1, 2:1, 1:1, 1:2, 1:3) were confirmed by Energy Dispersive X-ray Analysis (EDAX). X-ray diffraction (XRD) structural characterization data shows that the Pt-CeO(2)/C catalysts are composed of nanosized polycrystalline non-alloyed deposits, from which reflections corresponding to the fcc (Pt) and fluorite (CeO(2)) structures were clearly observed. The mean crystallite sizes calculated from XRD data revealed that, independent of the mass ratio, a value close to 3 nm was obtained for the CeO(2) particles. For Pt, the mean crystallite sizes were dependent on the ratio of this metal in the catalysts. Low platinum ratios resulted in small crystallites. and high Pt proportions resulted in larger crystallites. The size distributions of the catalysts particles, determined by XRD, were confirmed by Transmission Electron Microscope (TEM) imaging. Cyclic voltammetry and chronoamperometic experiments were used to evaluate the electrocatalytic performance of the different materials. In all cases, except Pt-CeO(2)/C 1:1, the Pt-Ceo(2)/C catalysts exhibited improved performance when compared with Pt/C. The best result was obtained for the Pt-CeO(2)/C 1:3 catalyst, which gave better results than the Pt-Ru/C (Etek) catalyst. (C) 2009 Elsevier B.V. All rights reserved.
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Print No: 66.; Initials Lower Right: ELW (Everett Longley Warner)
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Print No:80.; Initials Lower Right: ELW (Everett Longley Warner)