Impacte de la SIDA sobre el creixement econòmic de l'Àfrica

Aquest treball tracta, des d’una perspectiva general, sobre quin impacte té el virus del VIH sobre el creixement econòmic dels països africans. Per a veure com evoluciona una economia, s’ha pres com a mesura el PIB per càpita, ja que es tracta d’una mesura que no té en compte el tamany dels estats, sinó que permet veure de manera més directa com pateix la malaltia la població.Partint d’una hipòtesi en forma de pregunta, i després d’una introducció a la malaltia i la seva situació en l’actualitat, se separa l’anàlisi dels efectes microeconòmics de la dels macroeconòmics, per acabar enllaçant-les i il·lustrant-les amb una senzilla explicació seguint el model de creixement de Solow. La conclusió a la qual s’arriba és que, a llarg termini, la SIDA comporta unes conseqüències clarament negatives sobre l’economia de l’Àfrica i que, a més a més, requereixen d’una resposta urgent a nivell global per evitar-les.

Infoquiniela

Al plantejar-nos aquest treball volíem que estigués relacionat amb coneixements que ja hem estudiat i a la vegada profunditzar en ells, però a més, tenir l’oportunitat d’introduir-nos en nous temes, com el màrqueting o la creació de l’empresa.Després d’estudiar diverses opcions, vàrem decidir estudiar la viabilitat de una empresarelacionada amb dos temes centrals: Internet i futbol. Amb el primer hi estem contínuament en contacte i ens interessava veure les possibilitats que dona la xarxa a l’hora de desenvolupar un negoci i a lavegada quins costos implica. Per l’altra banda, el futbol és un esport que ens agrada i sabem que hi ha un gran volum de persones interessades en aquest esport i que a més realitzen travesses, l’objecte de la nostra empresa.A partir d’aquí, analitzarem el mercat, coneixerem tots els requisits necessaris per crear una empresa, decidirem el tipus d’inversió que necessita aquest projecte i veurem per últim la viabilitat delprojecte comparant els costos i ingressos que s’enfrontarà l’empresa durant 4 anys.

Analog circuit for real-time computation of respiratory mechanical impedance in sleep studies

The aim of this work was to develop a low-cost circuit for real-time analog computation of the respiratory mechanical impedance in sleep studies. The practical performance of the circuit was tested in six patients with obstructive sleep apnea. The impedance signal provided by the analog circuit was compared with the impedance calculated simultaneously with a conventional computerized system. We concluded that the low-cost analog circuit developed could be a useful tool for facilitating the real-time assessment of airway obstruction in routine sleep studies.

Effect of expiratory flow limitation on respiratory mechanical impedance: a model study

Large phasic variations of respiratory mechanical impedance (Zrs) have been observed during induced expiratory flow limitation (EFL) (M. Vassiliou, R. Peslin, C. Saunier, and C. Duvivier. Eur. Respir. J. 9: 779-786, 1996). To clarify the meaning of Zrs during EFL, we have measured from 5 to 30 Hz the input impedance (Zin) of mechanical analogues of the respiratory system, including flow-limiting elements (FLE) made of easily collapsible rubber tubing. The pressures upstream (Pus) and downstream (Pds) from the FLE were controlled and systematically varied. Maximal flow (Vmax) increased linearly with Pus, was close to the value predicted from wave-speed theory, and was obtained for Pus-Pds of 4-6 hPa. The real part of Zin started increasing abruptly with flow (V) >85%Vmax and either further increased or suddenly decreased in the vicinity of V¿max. The imaginary part of Zin decreased markedly and suddenly above 95%Vmax. Similar variations of Zin during EFL were seen with an analogue that mimicked the changes of airway transmural pressure during breathing. After pressure andV measurements upstream and downstream from the FLE were combined, the latter was analyzed in terms of a serial (Zs) and a shunt (Zp) compartment. Zs was consistent with a large resistance and inertance, and Zp with a mainly elastic element having an elastance close to that of the tube walls. We conclude that Zrs data during EFL mainly reflect the properties of the FLE.

Thrombin-induced contraction in alveolar epithelial cells probed by traction microscopy

Contractile tension of alveolar epithelial cells plays a major role in the force balance that regulates the structural integrity of the alveolar barrier. The aim of this work was to study thrombin-induced contractile forces of alveolar epithelial cells. A549 alveolar epithelial cells were challenged with thrombin, and time course of contractile forces was measured by traction microscopy. The cells exhibited basal contraction with total force magnitude 55.0 ± 12.0 nN (mean ± SE, n = 12). Traction forces were exerted predominantly at the cell periphery and pointed to the cell center. Thrombin (1 U/ml) induced a fast and sustained 2.5-fold increase in traction forces, which maintained peripheral and centripetal distribution. Actin fluorescent staining revealed F-actin polymerization and enhancement of peripheral actin rim. Disruption of actin cytoskeleton with cytochalasin D (5 µM, 30 min) and inhibition of myosin light chain kinase with ML-7 (10 µM, 30 min) and Rho kinase with Y-27632 (10 µM, 30 min) markedly depressed basal contractile tone and abolished thrombin-induced cell contraction. Therefore, the contractile response of alveolar epithelial cells to the inflammatory agonist thrombin was mediated by actin cytoskeleton remodeling and actomyosin activation through myosin light chain kinase and Rho kinase signaling pathways. Thrombin-induced contractile tension might further impair alveolar epithelial barrier integrity in the injured lung.

A new estimator to minimize the error due to breathing in the measurement of respiratory impedance

This paper presents a new respiratory impedance estimator to minimize the error due to breathing. Its practical reliability was evaluated in a simulation using realistic signals. These signals were generated by superposing pressure and flow records obtained in two conditions: 1) when applying forced oscillation to a resistance- inertance- elastance (RIE) mechanical model; 2) when healthy subjects breathed through the unexcited forced oscillation generator. Impedances computed (4-32 Hz) from the simulated signals with the new estimator resulted in a mean value which was scarcely biased by the added breathing (errors less than 1 percent in the mean R, I , and E ) and had a small variability (coefficients of variation of R, I, and E of 1.3, 3.5, and 9.6 percent, respectively). Our results suggest that the proposed estimator reduces the error in measurement of respiratory impedance without appreciable extracomputational cost.

An introduction to Mediterranean deep-sea biology

This chapter presents the state of the art concerning the deep-sea Mediterranean environment: geology, hydrology, biology and fisheries. These are the fields of study dealt with in the scientific papers of this volume. The authors are specialists who have addressed their research to the Mediterranean deep-sea environment during the last years. This introduction is an overview but not an exhaustive review.

Analog circuit for real-time computation of respiratory mechanical impedance in sleep studies

The aim of this work was to develop a low-cost circuit for real-time analog computation of the respiratory mechanical impedance in sleep studies. The practical performance of the circuit was tested in six patients with obstructive sleep apnea. The impedance signal provided by the analog circuit was compared with the impedance calculated simultaneously with a conventional computerized system. We concluded that the low-cost analog circuit developed could be a useful tool for facilitating the real-time assessment of airway obstruction in routine sleep studies.

Corticosterone inhibits the lipid-mobilizing effects of oleoyl-estrone in adrenalectomized rats

Oleoyl-estrone (OE) is an adipose-derived signal that decreases energy intake and body lipid, maintaining energy expenditure and glycemic homeostasis. Glucocorticoids protect body lipid and the metabolic status quo. We studied the combined effects of OE and corticosterone in adrenalectomized female rats: daily OE gavages (0 or 10 nmol/g) and slow-release corticosterone pellets at four doses (0, 0.5, 1.7, and 4.8 mg/d). Intact and sham-operated controls were also included. After 8 d, body composition and plasma metabolites and hormones were measured. OE induced a massive lipid mobilization (in parallel with decreased food intake and maintained energy expenditure). Corticosterone increased fat deposition and inhibited the OE-elicited mobilization of body energy, even at the lowest dose. OE enhanced the corticosterone-induced rise in plasma triacylglycerols, and corticosterone blocked the OE-induced decrease in leptin. High corticosterone and OE increased insulin resistance beyond the effects of corticosterone alone. The presence of corticosterone dramatically affected OE effects, reversing its decrease of body energy (lipid) content, with little or no change on food intake or energy expenditure. The maintenance of glycemia and increasing insulin in parallel to the dose of corticosterone indicate a decrease in insulin sensitivity, which is enhanced by OE. The reversal of OE effects on lipid handling, insulin resistance, can be the consequence of a corticosterone-induced OE resistance. Nevertheless, OE effects on cholesterol were largely unaffected. In conclusion, corticosterone administration effectively blocked OE effects on body lipid and energy balance as well as insulin sensitivity and glycemia.

In rats, oral oleoyl-DHEA is rapidly hydrolysed and converted to DHEA-sulphate

Background: Dehydroepiandrosterone (DHEA) released by adrenal glands may be converted to androgens and estrogens mainly in the gonadal, adipose, mammary, hepatic and nervous tissue. DHEA is also a key neurosteroid and has antiglucocorticoid activity. DHEA has been used for the treatment of a number of diseases, including obesity; its pharmacological effects depend on large oral doses, which effect rapidly wanes in part because of its short half-life in plasma. Since steroid hormone esters circulate for longer periods, we have studied here whether the administration of DHEA oleoyl ester may extend its pharmacologic availability by keeping high circulating levels. Results: Tritium-labelled oleoyl-DHEA was given to Wistar male and female rats by gastric tube. The kinetics of appearance of the label in plasma was unrelated to sex; the pattern being largely coincident with the levels of DHEA-sulfate only in females, and after 2 h undistinguishable from the results obtained using labelled DHEA gavages; in the short term, practically no lipophilic DHEA label was found in plasma. After 24 h only a small fraction of the label remained in the rat organs, with a different sex-related distribution pattern coincident for oleoyl- and free- DHEA gavages. The rapid conversion of oleoyl-DHEA into circulating DHEA-sulfate was investigated using stomach, liver and intestine homogenates; which hydrolysed oleoyl-DHEA optimally near pH 8. Duodenum and ileum contained the highest esterase activities. Pure hog pancreas cholesterol-esterase broke down oleoyl-DHEA at rates similar to those of oleoyl-cholesterol. The intestinal and liver esterases were differently activated by taurocholate and showed different pH-activity patterns than cholesterol esterase, suggesting that oleoyl-DHEA can be hydrolysed by a number of esterases in the lumen (e.g. cholesterol-esterase), in the intestinal wall and the liver. Conclusion: The esterase activities found may condition the pharmacological availability (and depot effect) of orally administered steroid hormone fatty acid esters such as oleoyl-DHEA. The oral administration of oleoyl-DHEA in order to extend DHEA plasma availability has not been proved effective, since the ester is rapidly hydrolysed, probably in the intestine itself, and mainly converted to DHEA-sulfate at least in females.

Semiquantitative RT-PCR measurement of gene expression in rat tissues including a correction for varying cell size and number

Background: Current methodology of gene expression analysis limits the possibilities of comparison between cells/tissues of organs in which cell size and/or number changes as a consequence of the study (e.g. starvation). A method relating the abundance of specific mRNA copies per cell may allow direct comparison or different organs and/or changing physiological conditions. Methods: With a number of selected genes, we analysed the relationship of the number of bases and the fluorescence recorded at a present level using cDNA standards. A lineal relationship was found between the final number of bases and the length of the transcript. The constants of this equation and those of the relationship between fluorescence and number of bases in cDNA were determined and a general equation linking the length of the transcript and the initial number of copies of mRNA was deduced for a given pre-established fluorescence setting. This allowed the calculation of the concentration of the corresponding mRNAs per g of tissue. The inclusion of tissue RNA and the DNA content per cell, allowed the calculation of the mRNA copies per cell. Results: The application of this procedure to six genes: Arbp, cyclophilin, ChREBP, T4 deiodinase 2, acetyl-CoA carboxylase 1 and IRS-1, in liver and retroperitoneal adipose tissue of food-restricted rats allowed precise measures of their changes irrespective of the shrinking of the tissue, the loss of cells or changes in cell size, factors that deeply complicate the comparison between changing tissue conditions. The percentage results obtained with the present methods were essentially the same obtained with the delta-delta procedure and with individual cDNA standard curve quantitative RT-PCR estimation. Conclusion: The method presented allows the comparison (i.e. as copies of mRNA per cell) between different genes and tissues, establishing the degree of abundance of the different molecular species tested.

Didàctica de la llengua i la literatura. Experiències d'innovació docent a la Universitat. Presentació

Totes les universitats de l'Estat Espanyol es troben immerses en el procés d'implantació dels nous estudis de grau i postgrau adaptats a l'Espai Europeu d'Educació Superior (EEES). Aquest procés ¿conegut popularment amb el nom de Pla Bolonya¿ ha suscitat un amplíssim debat, centrat fonamentalment en el paper que ha derepresentar la universitat en la societat tecnològica i globalitzada del segle XXI. Nombroses veus d'experts en àmbits molt diversos han posat de relleu les dificultats que comporta definir i tirar endavant el Pla Bolonya i han alertat dels perills que comporta la seva aplicació, sobretot per la supeditació als dictats del mercat (mercantilització) i pel que alguns han anomenat la "pèrdua de les humanitats". Serveixin com a exempled'aquests posicionaments les paraules de N. López Calera en una publicació recent sobre la innovació a la universitat: "El Plan Bolonia ha evitado que se hiciera una filosofía de las universidades y, en últimainstancia, de la educación y de la cultura. Ha limitado las perspectivas a lo que la universidad "tiene que ser" de acuerdo con las exigencias del desarrollo económico y el progreso tecnológico de las sociedades de nuestro tiempo. La universidad no debe ser una cuestión de estrategias de productividad y rentabilidad" ...

Teràpia aquàtica en pacients afectats d' AVC

La teràpia aquàtica o hidroteràpia és una de les tècniques de fisioteràpia poc valorades pels beneficis que aporten. En aquest estudi analitzem com aquest tractament en el medi aquàtic pot beneficiar als pacients afectats de un accident vascular cerebral (AVC). Els participants d’aquest estudi son pacients els quals han patit un AVC en els últims dos anys. Aquest estudi serà dut a terme ha l’Hospital Sant Joan de Déu de Palma de Mallorca. La investigació consisteix en una combinació entre el mètode qualitatiu i el mètode quantitatiu, cada mètode aporta diferents visions de l’estudi amb la finalitat d’obtenir resultats més complets, arribant als objectius marcats. Per una banda, l’aspecte bio-psico-social serà avaluat utilitzant el mètode qualitatiu, realitzant entrevistes semi-estructures abans i després del tractament amb la finalitat d’obtenir la sensació que percep el pacient en cada moment. Per l’altre banda, l’espasticitat la valorarem mitjançant l’escala de Ashworth amb el mètode quantitatiu abans i després del tractament. Tenint en compte que poden sorgir varis limitacions com el temps de durada de l’estudi, la planificació o limitacions entre els participants, és un estudi interessant per valorar els canvis en la qualitat de vida d’aquestes persones.