Hydrophobic labeling of (Na+,K+)-ATPase: further evidence that the beta subunit is embedded in the membrane bilayer.

O-Hexanoyl-3,5-diiodo-N-(4-azido-2-nitro-phenyl)tyramine has been used after photochemical conversion into the reactive nitrene to label (Na+,K+)-ATPase from Bufo marinus toad kidney. Immunochemical evidence indicates that the reagent labels both subunits of the enzyme in partially purified form as well as in microsomal membranes. These results support the view that the glycoprotein subunit, like the catalytic subunit, possesses hydrophobic domains by which it is integrated into the plasma membrane.

Le traitement religieux par les médias

Depuis le début de cette décennie, les médias accordent un intérêt croissant au religieux. Cet intérêt évolue en relation étroite avec le changement socioculturel qui affecte aussi bien le champ de la communication de masse que celui de la religion. On ne s'étonnera pas dès lors, explique l'A., d'observer que la mise en scène du religieux par les médias échappe, partiellement du moins, au contrôle des institutions religieuses, même les mieux organisées, et obéisse aux lois qui régulent leur langage.

FXYD7 is a brain-specific regulator of Na,K-ATPase alpha 1-beta isozymes.

Recently, corticosteroid hormone-induced factor (CHIF) and the gamma-subunit, two members of the FXYD family of small proteins, have been identified as regulators of renal Na,K-ATPase. In this study, we have investigated the tissue distribution and the structural and functional properties of FXYD7, another family member which has not yet been characterized. Expressed exclusively in the brain, FXYD7 is a type I membrane protein bearing N-terminal, post-translationally added modifications on threonine residues, most probably O-glycosylations that are important for protein stabilization. Expressed in Xenopus oocytes, FXYD7 can interact with Na,K-ATPase alpha 1-beta 1, alpha 2-beta 1 and alpha 3-beta 1 but not with alpha-beta 2 isozymes, whereas, in brain, it is only associated with alpha 1-beta isozymes. FXYD7 decreases the apparent K(+) affinity of alpha 1-beta 1 and alpha 2-beta 1, but not of alpha 3-beta1 isozymes. These data suggest that FXYD7 is a novel, tissue- and isoform-specific Na,K-ATPase regulator which could play an important role in neuronal excitability.

Medida de la Velocidad de Onda de Pulso mediante Ecografía Doppler: Concordancia con el Método Complior

La rigidez arterial es un parámetro establecido dentro de la valoración del riesgo cardio-vascular. Actualmente disponemos de múltiples métodos para determinar la velocidad de onda de pulso (VOP) y entre ellos los más utilizados son los métodos mecánicos, como el Complior o el Sphigmocor, que precisan de dispositivos específicos y una inversión importante en aprendizaje y tiempo de exploración. La utilización del doppler guiado por ecografía 2D es una buena alternativa a estos métodos. Realizamos un estudio comparativo para evaluar la fiabilidad del eco-doppler en la medida de la VOP carótida-femoral respecto al método Complior. Se estudió la VOP carótida-femoral utilizando los dos sistemas en 40 pacientes, mostrando ambos métodos muy buena concordancia (R=0’91). En el análisis de reproducibilidad de la VOP por doppler no se hallaron diferencias intra e interobservador. En base a los resultados, el estudio demuestra que la ecografía doppler puede ser usada para medir la VOP aórtica de manera fiable y reproducible, similar otros métodos más establecidos.

WEB Cas Pràctic boo-k : Gestió d'una Botiga Virtual

L'objectiu d'aquest treball és especificar, dissenyar i implementar una aplicació web que permeti l'operativa real dels serveis de gestió d'una botiga virtual d'Internet, amb el suport d'un sistema de gestió de bases de dades.

Método alternativo a la modelización gráfica en el cálculo del espacio necesario para crear zonas lineales de aparcamiento en vías urbanas

Aquest mètode permet calcular numèricament l¿espai necessari per crear zones lineals d¿aparcament d¿ n places sense haver de recórrer a la modelització gràfica. Està dissenyat especialment per trobar amb facilitat les característiques òptimes de zones d¿aparcament en vies amb limitacions d¿espai. Aquest estudi és una anàlisi trigonomètrica d¿una àrea d¿aparcament tenint en compte el comportament d¿un vehicle estàndard en la maniobra d¿estacionament.

Médiatiser la police. Policer les médias

Le travail policier est depuis longtemps l'objet de récits etd'images qui ont durablement influencé notre imaginaire.Cette puissance narrative acquise fait aujourd'hui del'univers policier l'un des arrière-plans préférés des médias.À partir de ce constat, cet ouvrage se propose d'explorercomment des représentations de la police sont produiteset circulent dans, et entre, les champs du divertissement etde l'information, mais également comment l'institutionpolicière s'est elle-même constituée en pourvoyeuse et engardienne de son « image publique ». Plus que jamais, lemonde réel et le monde médiatique de la police coexistentet se confrontent, car les corps de police sont devenus desproducteurs actifs d'images et de discours sur leurspropres actions.Par un double mouvement, «médiatiser la police » et«policer les médias », ce livre étudie l'imaginaire social surla police, sa diffusion dans les médias de masse (télévision,presse, affiches, espaces muséaux...) ainsi que le travailcommunicationnel des polices modernes.

Mejora diagnóstica de hepatopatías de afectación difusa mediante técnicas de inteligencia artificial

The automatic diagnostic discrimination is an application of artificial intelligence techniques that can solve clinical cases based on imaging. Diffuse liver diseases are diseases of wide prominence in the population and insidious course, yet early in its progression. Early and effective diagnosis is necessary because many of these diseases progress to cirrhosis and liver cancer. The usual technique of choice for accurate diagnosis is liver biopsy, an invasive and not without incompatibilities one. It is proposed in this project an alternative non-invasive and free of contraindications method based on liver ultrasonography. The images are digitized and then analyzed using statistical techniques and analysis of texture. The results are validated from the pathology report. Finally, we apply artificial intelligence techniques as Fuzzy k-Means or Support Vector Machines and compare its significance to the analysis Statistics and the report of the clinician. The results show that this technique is significantly valid and a promising alternative as a noninvasive diagnostic chronic liver disease from diffuse involvement. Artificial Intelligence classifying techniques significantly improve the diagnosing discrimination compared to other statistics.

Access of extracellular cations to their binding sites in Na,K-ATPase: role of the second extracellular loop of the alpha subunit.

Na,K-ATPase, the main active transport system for monovalent cations in animal cells, is responsible for maintaining Na(+) and K(+) gradients across the plasma membrane. During its transport cycle it binds three cytoplasmic Na(+) ions and releases them on the extracellular side of the membrane, and then binds two extracellular K(+) ions and releases them into the cytoplasm. The fourth, fifth, and sixth transmembrane helices of the alpha subunit of Na,K-ATPase are known to be involved in Na(+) and K(+) binding sites, but the gating mechanisms that control the access of these ions to their binding sites are not yet fully understood. We have focused on the second extracellular loop linking transmembrane segments 3 and 4 and attempted to determine its role in gating. We replaced 13 residues of this loop in the rat alpha1 subunit, from E314 to G326, by cysteine, and then studied the function of these mutants using electrophysiological techniques. We analyzed the results using a structural model obtained by homology with SERCA, and ab initio calculations for the second extracellular loop. Four mutants were markedly modified by the sulfhydryl reagent MTSET, and we investigated them in detail. The substituted cysteines were more readily accessible to MTSET in the E1 conformation for the Y315C, W317C, and I322C mutants. Mutations or derivatization of the substituted cysteines in the second extracellular loop resulted in major increases in the apparent affinity for extracellular K(+), and this was associated with a reduction in the maximum activity. The changes produced by the E314C mutation were reversed by MTSET treatment. In the W317C and I322C mutants, MTSET also induced a moderate shift of the E1/E2 equilibrium towards the E1(Na) conformation under Na/Na exchange conditions. These findings indicate that the second extracellular loop must be functionally linked to the gating mechanism that controls the access of K(+) to its binding site.