Investigaciones realizadas en la Universidad de Aveiro sobre caracterización mecánica de las construcciones existentes en adobe en Portugal y propuestas de rehabilitación y refuerzo. Resultados alcanzados

En Portugal, sobre todo en la región de Aveiro, las estructuras de fábrica de adobe fueron el sistema constructivo predominante durante la primera mitad del siglo XX. En la actualidad es aún significativo el legado del patrimonio – cerca de 30% de las construcciones existentes – el cual está formado por un conjunto significativo de construcciones de elevado valor histórico y arquitectónico. En las últimas décadas se ha descuidado su rehabilitación, que ha redundado en el estado actual de daño en muchas de estas construcciones, con desfavorables condiciones de seguridad, y en algunos casos comprometiendo su uso. No obstante, en los últimos años, se observa un creciente interés, asociado a factores ambientales, económicos y de salvaguarda del patrimonio, tanto por parte de las administraciones locales como en el ámbito de los inversores privados, por la conservación y rehabilitación de estas construcciones. Ante esta nueva realidad, que pone de manifiesto la necesidad de desarrollar soluciones y técnicas de intervención que permitan, a través de la rehabilitación y/o refuerzo, prolongar la vida útil de estas estructuras, en la Universidad de Aveiro un grupo de investigadores viene desarrollando un trabajo multidisciplinar sobre las construcciones de adobe en Portugal. El objetivo principal del mismo se centra en la creación de una base de resultados experimentales que apoye las intervenciones de rehabilitación y/o refuerzo del patrimonio edificado, y el desarrollo de soluciones de mejora de su comportamiento estructural. Esta investigación se constituye como un guía que procura contribuir al conocimiento de estas fábricas, enfocado sobre todo a la rehabilitación de las mismas, aportando información que permita a los diferentes profesionales que trabajan en este ámbito actuar en la conservación de este patrimonio

Estudio y propuestas en materia de prevención de riesgos laborales para el Laboratorio de investigaciones metalográficas y metalotecnia

En este trabajo se estudian y detallan , bajo el punto de vista de los riesgos laborales, los riesgos que suponen para los trabajadores los principales procesos , equipos y máquinas que se emplean en el Laboratorio Oficial de Investigaciones Metalográficas de la ETSI Minas y Energía- UPM (LIMM) ya sean mecánicos, químicos, físicos o eléctricos. Además de los riesgos específicos citados debemos tener en cuenta que el personal del laboratorio también se ve sometido a riesgos por manipulación de cargas de forma repetitiva y continuada. El estudio y las propuestas en materia de prevención de riesgos laborales de este proyecto han sido elaboradas para cumplir con las medidas de protección necesarias como queda establecido en el artículo 14 de la Ley de Prevención de Riesgos Laborales - Ley 31/1995 sobre el derecho a la protección frente a los riesgos laborales para garantizar la seguridad y salud de las personas que realizan las actividades del laboratorio. El objetivo es presentar propuestas correctoras frente a los riesgos encontrados para erradicar el número de accidentes laborales que se han materializado o que pueden llegar a producirse a causa de unas deficientes condiciones de trabajo, estas propuestas ofrecen las medidas correctoras de tipo colectivo, prioritarias en cualquier plan de prevención de riesgos laborales, como medidas de tipo individual o particular, los llamados EPIs (equipos de protección individual). En primer lugar se actúa sobre el foco de origen del riesgo, si no fuera posible sobre el medio de propagación y si ninguna de las anteriores medidas se pudiera llevar a cabo sobre las personas que se encuentran en contacto.

Reflexión y refracción de la luz en medios anisótropos

En este proyecto se pretende estudiar el comportamiento de la luz al atravesar medios de diversos materiales, tanto isótropos como anisótropos uniáxicos. Para ello se requiere realizar un estudio previo de las condiciones de contorno aplicables a las ecuaciones de Maxwell en la interfase de dos medios que pueden ser isótropos o anisótropos. En el caso de dos materiales isótropos, la solución del problema son los conocidos coeficientes de Fresnel de reflexión y transmisión. En este trabajo se pretende generalizar el estudio al caso del paso de la luz desde un medio isótropo a otro anisótropo uniáxico (con su eje óptico en orientación arbitraria) y viceversa y al caso de dos materiales anisótropos uniáxicos con ejes ópticos en orientaciones arbitrarias. Es de especial interés el caso de un mismo material uniáxico en el que las dos partes tienen el eje óptico con distinta orientación. Una vez planteadas las condiciones de contorno específicas en cada caso, se obtendrá un conjunto de ecuaciones algebraicas cuya resolución permitirá obtener los coeficientes de reflexión y transmisión buscados. Para plantear el sistema de ecuaciones adecuado, será necesario tener una descripción de las características ópticas de los materiales empleados, la orientación de los ejes ópticos en cada caso, y los posibles ángulos de incidencia. Se realizará un tratamiento matricial de modo que el paquete MatLab permite su inversión de manera inmediata. Se desarrollará una interfaz sencilla, realizada con MatLab, que permita al usuario introducir sin dificultad los datos correspondientes a los materiales de los medios incidente y transmitido, la orientación en espacial del o de los ejes ópticos, de la longitud de onda de trabajo y del ángulo de incidencia del haz de luz, con los que la aplicación realizará los cálculos. Los coeficientes de reflexión y refracción obtenidos serán representados gráficamente en función del ángulo de incidencia. Así mismo se representarán los ángulos transmitidos y reflejados en función del de incidencia. Todo ello de esta forma, que resulte sencilla la interpretación de los datos por parte del usuario. ABSTRACT. The reason for this project is to study the behavior of light when light crosses different media of different materials, isotropic materials and uniaxial anisotropic materials. For this, a previous study is necessary where the boundary conditions apply to Maxwell equations at the interface between two media which can be isotropic and anisotropic. If both materials are isotropic, the Fresnel ccoefficients of reflection and refraction are used to solve the problem. The aim of this work is to generalize a study when light crosses from an isotropic media to a uniaxial anisotropic media, where its axis have arbitrary directions, and vicecersa. The system consisting of two materials with axis in arbitrary directions are also being studied. Once the specific boundary conditions are known in each case, a set of algebraic equations are obtained whose solution allows obtaining the reflection coefficients and refraction coefficients. It is necessary to have a description of the optical characteristics of the materials used; of the directions axis in each case and the possible angle of incidence. A matrix is proposed for later treatment in Matlab that allows the immediate inversion. A simple interface will de developed, manufactured with Matlab, that allows the user to enter data easily corresponding to the incident media and transmission media of the different materials, the special axis directions, the wavelength and the angle of incidence of the light beam. This data is used by the application to perform the necessary calculations to solve the problem. When reflection coefficients and refraction coefficients are obtained, the application draws the graphics in function of the angle of incidence. Also transmitted and reflected angles depending on the incidence are represented. This is to perform a data representation which is a simple interpretation of the user data.

Comentarios al libro Paisajes mineros antiguos en la Península Ibérica: investigaciones recientes y nuevas líneas de trabajo

El título del libro es el mismo que el de una reunión científica celebrada en Almadén (21-23 de marzo de 2012) y en la que se rindió homenaje a Claude Domergue, profesor emérito de la Universidad de Toulouse, pionero de la Arqueología Minera española y socio honorario de SEDPGYM. Esta obra fue editada por la UNED, en el mismo año, bajo la dirección de Mar Zarzalejos Prieto, Patricia Hevia Gómez y Luis Mansilla Plaza, todos ellos socios nuestros

Dynamic characteristics and adaptability of mouse vestibulo-ocular and optokinetic response eye movements and the role of the flocculo-olivary system revealed by chemical lesions

The dynamic characteristics of reflex eye movements were measured in two strains of chronically prepared mice by using an infrared television camera system. The horizontal vestibulo-ocular reflex (HVOR) and horizontal optokinetic response (HOKR) were induced by sinusoidal oscillations of a turntable, in darkness, by 10° (peak to peak) at 0.11–0.50 Hz and of a checked-pattern screen, in light, by 5–20°at 0.11–0.17 Hz, respectively. The gains and phases of the HVOR and HOKR of the C57BL/6 mice were nearly equivalent to those of rabbits and rats, whereas the 129/Sv mice exhibited very low gains in the HVOR and moderate phase lags in the HOKR, suggesting an inherent sensory-motor anomaly. Adaptability of the HOKR was examined in C57BL/6 mice by sustained screen oscillation. When the screen was oscillated by 10° at 0.17 Hz, which induced sufficient retinal slips, the gain of the HOKR increased by 0.08 in 1 h on average, whereas the stimuli that induced relatively small or no retinal slips affected the gain very little. Lesions of the flocculi induced by local applications of 0.1% ibotenic acid and lesions of the inferior olivary nuclei induced by i.p. injection of 3-acetylpyridine in C57BL/6 mice little affected the dynamic characteristics of the HVOR and HOKR, but abolished the adaptation of the HOKR. These results indicate that the olivo-floccular system plays an essential role in the adaptive control of the ocular reflex in mice, as suggested in other animal species. The data presented provide the basis for analyzing the reflex eye movements of genetically engineered mice.

A release mechanism for stored ATP in ocular ciliary epithelial cells

Purines can modify ciliary epithelial secretion of aqueous humor into the eye. The source of the purinergic agonists acting in the ciliary epithelium, as in many epithelial tissues, is unknown. We found that the fluorescent ATP marker quinacrine stained rabbit and bovine ciliary epithelia but not the nerve fibers in the ciliary bodies. Cultured bovine pigmented and nonpigmented ciliary epithelial cells also stained intensely when incubated with quinacrine. Hypotonic stimulation of cultured epithelial cells increased the extracellular ATP concentration by 3-fold; this measurement underestimates actual release as the cells also displayed ecto-ATPase activity. The hypotonically triggered increase in ATP was inhibited by the Cl−-channel blocker 5-nitro-2-(3-phenylpropylamino)benzoic acid (NPPB) in both cell types. In contrast, the P-glycoprotein inhibitors tamoxifen and verapamil and the cystic fibrosis transmembrane conductance regulator (CFTR) blockers glybenclamide and diphenylamine-2-carboxylate did not affect ATP release from either cell type. This pharmacological profile suggests that ATP release is not restricted to P-glycoprotein or the cystic fibrosis transmembrane conductance regulator, but can proceed through a route sensitive to NPPB. ATP release also was triggered by ionomycin through a different NPPB-insensitive mechanism, inhibitable by the calcium/calmodulin-activated kinase II inhibitor KN-62. Thus, both layers of the ciliary epithelium store and release ATP, and purines likely modulate aqueous humor flow by paracrine and/or autocrine mechanisms within the two cell layers of this epithelium.

Monitoring ocular hypertension, how much and how often? : A cost-effectiveness perspective

Peer reviewed

A model of ocular dominance column development by competition for trophic factor

Recent experimental evidence has shown that application of certain neurotrophic factors (NTs) to the developing primary visual cortex prevents the development of ocular dominance (OD) columns. One interpretation of this result is that afferents from the lateral geniculate nucleus compete for postsynaptic trophic factor in an activity-dependent manner. Application of excess trophic factor eliminates this competition, thereby preventing OD column formation. We present a model of OD column development, incorporating Hebbian synaptic modification and activity-driven competition for NT, which accounts for both normal OD column development as well as the prevention of that development when competition is removed. In the “control” situation, when available NT is below a critical amount, OD columns form normally. These columns form without weight normalization procedures and in the presence of positive inter-eye correlations. In the “experimental” case, OD column development is prevented in a local neighborhood in which excess NT has been added. Our model proposes a biologically plausible mechanism for competition between neural populations that is motivated by several pieces of experimental data, thereby accounting for both normal and experimentally perturbed conditions.

Subplate neuron ablation alters neurotrophin expression and ocular dominance column formation

Ocular dominance column formation in visual cortex depends on both the presence of subplate neurons and the endogenous expression of neurotrophins. Here we show that deletion of subplate neurons, which supply glutamatergic inputs to visual cortex, leads to a paradoxical increase in brain-derived neurotrophic factor mRNA in the same region of visual cortex in which ocular dominance columns are absent. Subplate neuron ablation also increases glutamic acid decarboxylase-67 levels, indicating an alteration in cortical inhibition. These observations imply a role for this special class of neurons in modulating activity-dependent competition by regulating levels of neurotrophins and excitability within a developing cortical circuit.

Ocular cicatricial pemphigoid antigen: Partial sequence and biochemical characterization

Ocular cicatricial pemphigoid (OCP) is an autoimmune disease that affects mainly conjunctiva and other squamous epithelia. OCP is histologically characterized by a separation of the epithelium from underlying tissues within the basement membrane zone. Immunopathological studies demonstrate the deposition of anti-basement membrane zone autoantibodies in vivo. Purified IgG from sera of patients with active OCP identified a cDNA clone from a human keratinocyte cDNA library that had complete homology with the cytoplasmic domain of β4-integrin. The sera recognized a 205-kDa protein in human epidermal, human conjunctiva, and tumor cell lysates that was identified as β4-integrin by its reaction with polyclonal and monoclonal antibodies to human β4-integrin. Sera from patients with bullous pemphigoid, pemphigus vulgaris, and cicatricial pemphigoid-like diseases did not recognize the 205-kDa protein, indicating the specificity of the binding. These data strongly implicate a role for human β4-integrin in the pathogenesis of OCP. It should be emphasized that multiple antigens in the basement membrane zone of squamous epithelia may serve as targets for a wide spectrum of autoantibodies observed in vesiculobullous diseases. Molecular definition of these autoantigens will facilitate the classification and characterization of subsets of cicatricial pemphigoid and help distinguishing them from bullous pemphigoid. This study highlights the function and importance of β4-integrin in maintaining the attachment of epithelial cells to the basement membrane.

Prevention of ischemia-induced retinopathy by the natural ocular antiangiogenic agent pigment epithelium-derived factor

Aberrant blood vessel growth in the retina that underlies the pathology of proliferative diabetic retinopathy and retinopathy of prematurity is the result of the ischemia-driven disruption of the normally antiangiogenic environment of the retina. In this study, we show that a potent inhibitor of angiogenesis found naturally in the normal eye, pigment epithelium-derived growth factor (PEDF), inhibits such aberrant blood vessel growth in a murine model of ischemia-induced retinopathy. Inhibition was proportional to dose and systemic delivery of recombinant protein at daily doses as low as 2.2 mg/kg could prevent aberrant endothelial cells from crossing the inner limiting membrane. PEDF appeared to inhibit angiogenesis by causing apoptosis of activated endothelial cells, because it induced apoptosis in cultured endothelial cells and an 8-fold increase in apoptotic endothelial cells could be detected in situ when the ischemic retinas of PEDF-treated animals were compared with vehicle-treated controls. The ability of low doses of PEDF to curtail aberrant growth of ocular endothelial cells without overt harm to retinal morphology suggests that this natural protein may be beneficial in the treatment of a variety of retinal vasculopathies.

Vaccination for protection of retinal ganglion cells against death from glutamate cytotoxicity and ocular hypertension: Implications for glaucoma

Our group recently demonstrated that autoimmune T cells directed against central nervous system-associated myelin antigens protect neurons from secondary degeneration. We further showed that the synthetic peptide copolymer 1 (Cop-1), known to suppress experimental autoimmune encephalomyelitis, can be safely substituted for the natural myelin antigen in both passive and active immunization for neuroprotection of the injured optic nerve. Here we attempted to determine whether similar immunizations are protective from retinal ganglion cell loss resulting from a direct biochemical insult caused, for example, by glutamate (a major mediator of degeneration in acute and chronic optic nerve insults) and in a rat model of ocular hypertension. Passive immunization with T cells reactive to myelin basic protein or active immunization with myelin oligodendrocyte glycoprotein-derived peptide, although neuroprotective after optic nerve injury, was ineffective against glutamate toxicity in mice and rats. In contrast, the number of surviving retinal ganglion cells per square millimeter in glutamate-injected retinas was significantly larger in mice immunized 10 days previously with Cop-1 emulsified in complete Freund's adjuvant than in mice injected with PBS in the same adjuvant (2,133 ± 270 and 1,329 ± 121, respectively, mean ± SEM; P < 0.02). A similar pattern was observed when mice were immunized on the day of glutamate injection (1,777 ± 101 compared with 1,414 ± 36; P < 0.05), but not when they were immunized 48 h later. These findings suggest that protection from glutamate toxicity requires reinforcement of the immune system by antigens that are different from those associated with myelin. The use of Cop-1 apparently circumvents this antigen specificity barrier. In the rat ocular hypertension model, which simulates glaucoma, immunization with Cop-1 significantly reduced the retinal ganglion cell loss from 27.8% ± 6.8% to 4.3% ± 1.6%, without affecting the intraocular pressure. This study may point the way to a therapy for glaucoma, a neurodegenerative disease of the optic nerve often associated with increased intraocular pressure, as well as for acute and chronic degenerative disorders in which glutamate is a prominent participant.

Involvement of integrins alpha v beta 3 and alpha v beta 5 in ocular neovascular diseases.

Angiogenesis underlies the majority of eye diseases that result in catastrophic loss of vision. Recent evidence has implicated the integrins alpha v beta 3 and alpha v beta 5 in the angiogenic process. We examined the expression of alpha v beta 3 and alpha v beta 5 in neovascular ocular tissue from patients with subretinal neovascularization from age-related macular degeneration or the presumed ocular histoplasmosis syndrome or retinal neovascularization from proliferative diabetic retinopathy (PDR). Only alpha v beta 3 was observed on blood vessels in ocular tissues with active neovascularization from patients with age-related macular degeneration or presumed ocular histoplasmosis, whereas both alpha v beta 3 and alpha v beta 5 were present on vascular cells in tissues from patients with PDR. Since we observed both integrins on vascular cells from tissues of patients with retinal neovascularization from PDR, we examined the effects of a systemically administered cyclic peptide antagonist of alpha v beta 3 and alpha v beta 5 on retinal angiogenesis in a murine model. This antagonist specifically blocked new blood vessel formation with no effect on established vessels. These results not only reinforce the concept that retinal and subretinal neovascular diseases are distinct pathological processes, but that antagonists of alpha v beta 3 and/or alpha v beta 5 may be effective in treating individuals with blinding eye disease associated with angiogenesis.

The ocular albinism type 1 gene product is a membrane glycoprotein localized to melanosomes.

Ocular albinism type 1 (OA1) is an inherited disorder characterized by severe reduction of visual acuity, photophobia, and retinal hypopigmentation. Ultrastructural examination of skin melanocytes and of the retinal pigment epithelium reveals the presence of macromelanosomes, suggesting a defect in melanosome biogenesis. The gene responsible for OA1 is exclusively expressed in pigment cells and encodes a predicted protein of 404 aa displaying several putative transmembrane domains and sharing no similarities with previously identified molecules. Using polyclonal antibodies we have identified the endogenous OA1 protein in retinal pigment epithelial cells, in normal human melanocytes and in various melanoma cell lines. Two forms of the OA1 protein were identified by Western analysis, a 60-kDa glycoprotein and a doublet of 48 and 45 kDa probably corresponding to unglycosylated precursor polypeptides. Upon subcellular fractionation and phase separation with the nonionic detergent Triton X-114, the OA1 protein segregated into the melanosome-rich fraction and behaved as an authentic integral membrane protein. Immunofluorescence and immunogold analyses on normal human melanocytes confirmed the melanosomal membrane localization of the endogenous OA1 protein, consistent with its possible involvement in melanosome biogenesis. The identification of a novel melanosomal membrane protein involved in a human disease will provide insights into the mechanisms that control the cell-specific pathways of subcellular morphogenesis.